CROSS REFERENCE TO RELATED APPLICATIONS

[0001] This application claims the benefit of U.S. Provisional Patent Application No. 62/425,752, filed November 23, 2016, the entirety of which is incorporated by reference.

TECHNICAL FIELD

[0002] The subject matter provided herein relates to folate receptor alpha (FRa)-specific antibodies as well as methods of using the antibodies to detect FRa and methods to diagnose, monitor, or treat FRa-expressing cancers.

BACKGROUND

[0003] In humans, the high affinity receptor for folate comes in four isoforms: alpha, beta, gamma, and delta. The alpha, beta and delta forms are typically bound to the membranes of cells by a glycosyl phosphatidylinositol (GPI) anchor. They recycle between extracellular and endocytic compartments and are capable of transporting folate into the cell. Soluble forms of folate receptor may be derived by the action of proteases or phospholipase on membrane anchored folate receptors.

[0004] Folate receptor alpha (also referred to as FRa, FR-alpha, FOLR-1 or FOLR1) is expressed in a variety of epithelial tissues, including those of the choroid plexus, lung, thyroid, kidney, uterus, breast, Fallopian tube, epididymis, and salivary glands. Weitman, S D et al, Cancer Res 52: 3396-3401 (1992); Weitman S D et al, Cancer Res 52: 6708-6711 (1992).

Overexpression of FRa has been observed in various cancers, including lung cancer (e.g., carcinoid tumors, and non-small cell lung cancers, such as adenocarcinomas); mesothelioma; ovarian cancer; renal cancer; brain cancer (e.g., anaplastic ependymoma, cerebellar juvenile pilocytic astrocytoma, and brain metastases); cervical cancer; nasopharyngeal cancer;

mesodermally derived tumor; squamous cell carcinoma of the head and neck; endometrial cancer; papillary serous and endometrioid adenocarcinomas of the ovary, serous cystadenocarcinomas of the ovary, breast cancer; bladder cancer; pancreatic cancer; bone cancer (e.g., high-grade osteosarcoma); pituitary cancer (e.g., pituitary adenomas); colorectal cancer and medullary thyroid cancer. See e.g. , U.S. Pat. No. 7,754,698; U.S. Patent Application No. 2005/0232919; Intl. Publ. No. WO 2009/132081; Bueno R et al, J of Thoracic and Cardiovascular Surgery, 121(2): 225-233 (2001); Elkanat H & Ratnam M. Frontiers in Bioscience, 11, 506-519 (2006); Basal et al., PLoS ONE, 4(7):6292 (2009); Fisher R E JNuclMed, 49: 899-906 (2008); Franklin, W A et al., Int J Cancer, Suppl 8: 89-95 (1994); Hartmann L C et al, Int J Cancer 121 : 938-942 (2007); Iwakiri S et al, Annals of Surgical Oncology, 15(3): 889-899 (2008); European patent publication EP 2199796, Parker N. et al, Analytical Biochemistry, 338: 284-293 (2005); Weitman, S D et al., Cancer Res 52: 3396-3401 (1992); Saba N F et al, Head Neck, 31(4): 475-481 (2009); Yang R et al., Clin Cancer Res 13: 2557-2567 (2007). In some types of cancers (e.g., squamous cell carcinoma of the head and neck), a high level of FRa expression is associated with a poor prognosis, whereas in other types of cancers (e.g., non-small-cell lung cancers), a higher level of FRa expression is associated with a more favorable prognosis. See, e.g., Iwakiri S et al, Annals of Surgical Oncology, 15(3): 889-899; Saba N F et al, Head Neck, 31(4): 475-481 (2009).

[0005] Earlier detection of cancer improves survival rates and quality of life. To improve the likelihood of early detection and treatment, a pressing need exists for non-invasive methods for diagnosing FRa-expressing cancers and for monitoring existing FRa-expressing cancers.

SUMMARY

[0006] Provided herein are antibodies that specifically bind to FRa. Also described are related polynucleotides capable of encoding the provided antibodies, cells expressing the provided antibodies, as well as associated vectors and detectable antibody labels. In addition, methods of using the provided antibodies to detect FRa and to diagnose, monitor, or treat ovarian cancer are described. For example, the provided antibodies may be used to diagnose, monitor or treat a folate receptor alpha-expressing cancer in a subject.

Folate Receptor Alpha (FRa)-Specific Antibodies

[0007] Described herein are isolated antibodies and antigen-binding fragments that specifically bind to FRa. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ

ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ

ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ

ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 9, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 10, wherein the CDR is defined according to the IMGT method.

[0008] In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO:

11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID

NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 12, wherein the

CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 13, wherein the CDR is defined according to the KABAT method.

[0009] In some embodiments, the antibodies or antigen-binding fragments are murine, IgG, chimeric or humanized.

[0010] In some embodiments, the antibodies or antigen-binding fragments include a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 6 and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 14 where the antibodies or antigen- binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method.

[0011] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 6, and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 14 where the antibodies or antigen- binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method.

[0012] Also disclosed are isolated antibodies or antigen-binding fragments specific for

FRa which include a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 6. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 14. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 6 and a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 14.

[0013] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 7. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 15. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 7 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 15.

[0014] In some embodiments, the FRa antibody is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 5, 2016 and assigned Accession No. PTA-123090.

[0015] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 21. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 29. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 21 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 29.

[0016] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 22. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 30. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 22 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 30.

[0017] Also disclosed are isolated polynucleotides that encode an antibody or antigen- binding fragment comprising a light chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 6. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a heavy chain variable region, wherein the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 14. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a light chain variable region and a heavy chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 6 and the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 14.

[0018] Also disclosed are isolated polynucleotides that encode an antibody or antigen- binding fragment comprising a light chain, wherein the light chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 7. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a heavy chain, wherein the heavy chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 15. In some embodiments, the isolated polynucleotides encode an antibody or antigen- binding fragment comprising a light chain and a heavy chain, wherein the light chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 7 and the heavy chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 15.

[0019] Described herein are isolated polynucleotides that encode an antibody or antigen- binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 1, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 2, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 3, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 8, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 9, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 1, wherein the CDR is defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 2, wherein the CDR is defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 3, wherein the CDR is defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 8, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 9, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 10, wherein the CDR is defined according to the IMGT method.

[0020] Described herein are isolated polynucleotides that encode an antibody or antigen- binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 4, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 5, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 3, a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 11, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 12, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 4, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 5, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 3, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 11, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 12, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 13, wherein the CDR is defined according to the KABAT method.

[0021] Described herein are isolated polynucleotide nucleotide sequences substantially similar to, or the same as, SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 23, SEQ ID NO: 24, and SEQ ID NO 25. In other embodiments, the isolated polynucleotides are substantially similar to, or the same as, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 18, SEQ ID NO: 26, SEQ ID NO: 27, and SEQ ID NO 28.

[0022] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein the light chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 1, the light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 2, and the light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence SEQ ID NO: 3, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 1, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 2, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated

polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 3, wherein the CDR is defined according to the IMGT method.

[0023] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein the light chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 4, the light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 5, and the light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence SEQ ID NO: 3, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 4, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 5, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 3, wherein the CDR is defined according to the KABAT method.

[0024] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein the heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 8, the heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 9, and the heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 8, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 9, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 10, wherein the CDR is defined according to the IMGT method.

[0025] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein the heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 11, the heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 12, and the heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence SEQ ID

NO: 13, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID

NO: 11, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID

NO: 12, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 13, wherein the CDR is defined according to the KABAT method.

[0026] In some embodiments the isolated polynucleotides capable of encoding the domains provided herein may be included on the same, or different, vectors to produce an antibody or antigen-binding fragment. Also provided are cells capable of expressing the described vectors. The cells may be eukaryotic cells, yeast cells, plant cells or bacteria. In preferred embodiments, the eukaryotic cell is a CHO cell.

Methods for Detecting Folate Receptor Alpha (FRa) in a Biological Sample

[0027] Provided herein are methods for detecting folate receptor alpha (FRa) in a biological sample. In some embodiments, the method involves exposing the sample to any one of the antibodies or antigen-binding fragments described herein and detecting FRa. In some embodiments, the biological sample is derived from urine, blood, serum, plasma, saliva, ascites, circulating cells, circulating tumor cells, cells that are not tissue associated, tissues, surgically resected tumor tissue, biopsies, fine needle aspiration samples, or histological preparations. In some embodiments, the biological sample is derived from a human or nonhuman primate. In some embodiments, the antibody is labeled. In some embodiments, the label is a radiolabel, an epitope tag, biotin, a chromophore label, a fluorophore label, an electrochemiluminescence (ECL) label, or an enzyme. In preferred embodiments, the electrochemiluminescence (ECL) label is a sulfo-tag. In some embodiments, the method further involves exposing the sample to a second antibody or antigen-binding fragment of any one of the described antibodies. In some embodiments, the second antibody or antigen-binding fragment is immobilized to a solid support.

In preferred embodiments, the second antibody or antigen-binding fragment is biotinylated and the solid support is coated with streptavidin, and the isolated antibody or antigen-binding fragment is immobilized to the solid support by the binding of biotin to streptavidin. In some embodiments, the presence of folate receptor alpha (FRa) in the sample is detected using westem blot, immunohistochemistry, immunofluorescence, flow cytometry, radioimmunoassay, immunoprecipitation, electrochemiluminescence immunoassay (ECLIA), or ELISA. In some embodiments, the sample is diluted prior to detecting folate receptor alpha (FRa) in the sample.

In some embodiments, the sample is centrifuged, vortexed, or both, prior to detecting folate receptor alpha (FRa) in the sample. In some embodiments, the level of folate receptor alpha

(FRa) in the sample is quantified. In some embodiments, the sample is exposed to MORAb-003 prior to detecting folate receptor alpha (FRa) in the sample. [0028] Also provided herein are methods for detecting folate receptor alpha (FRa) in a biological sample. In some embodiments, the method involves exposing the sample to a first isolated antibody or antigen-binding fragment comprising a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method, or a first isolated antibody or antigen- binding fragment comprising a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 5, 2016 that has been assigned Accession No. PTA-123090 and a second isolated antibody or antigen-binding fragment with a light chain CDRl comprising the amino acid sequence of SEQ ID NO: 31, a light chain CDR2 comprising the amino acid sequence of SEQ ID NO: 32, a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 33, a heavy chain CDRl comprising the amino acid sequence of SEQ ID NO: 35, a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 36, and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 37 or a second isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 19, 2011 that has been assigned Accession No. PTA- 11884, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[0029] In other embodiments, the method involves exposing the sample to a first isolated antibody or antigen-binding fragment with a light chain CDRl comprising the amino acid sequence of SEQ ID NO: 31, a light chain CDR2 comprising the amino acid sequence of SEQ ID

NO: 32, a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 33, a heavy chain CDRl comprising the amino acid sequence of SEQ ID NO: 35, a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 36, and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 37 or the isolated antibody that is produced by antibody- producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 19, 2011 that has been assigned Accession No. PTA-11884 and a second isolated antibody or antigen-binding fragment comprising a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method, or a second isolated antibody or antigen-binding fragment comprising a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method, or a second isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 5, 2016 that has been assigned Accession No. PTA- 123090, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[0030] In some embodiments, the biological sample is derived from urine, blood, serum, plasma, saliva, ascites, circulating cells, circulating tumor cells, cells that are not tissue associated, tissues, surgically resected tumor tissue, biopsies, fine needle aspiration samples, or histological preparations. In some embodiments, the biological sample is derived from a human or nonhuman primate. In some embodiments, the antibody is labeled. In some embodiments, the label is a radiolabel, an epitope tag, biotin, a chromophore label, a fluorophore label, an electrochemiluminescence (ECL) label, or an enzyme. In preferred embodiments, the electrochemiluminescence (ECL) label is a sulfo-tag. In some embodiments, the first isolated antibody or antigen-binding fragment is biotinylated and the solid support is coated with streptavidin, and the isolated antibody or antigen-binding fragment is immobilized to the solid support by the binding of biotin to streptavidin. In some embodiments, the presence of folate receptor alpha (FRa) in the sample is detected using western blot, immunohistochemistry, immunofluorescence, flow cytometry, radioimmunoassay, immunoprecipitation,

electrochemiluminescence immunoassay (ECLIA), or ELISA. In some embodiments, the level of FRa in the sample is quantified. In some embodiments, the sample is exposed to MORAb-003 prior to detecting folate receptor alpha (FRa) in the sample.

Methods for Diagnosing, Monitoring and Treating Folate Receptor Alpha (FRa)- Expressing Cancer

[0031] Provided herein are methods for diagnosing a folate receptor alpha (FRa)- expressing cancer in a subject. In some embodiments, the described methods involve exposing the biological sample of the subject to any one of the antibodies or antigen-binding fragments described herein. In some embodiments, the described methods involve exposing the biological sample of the subject to an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by any one of the antibodies or antigen binding fragments described herein. In some embodiments, the described methods involve quantifying the amount of FRa present in the sample that is bound by the antibody or antigen-binding fragment. In some embodiments, the described methods involve comparing the amount of FRa present in the sample to a known standard. In some embodiments, the described methods involve determining whether the subject's FRa levels fall within the levels of FRa associated with cancer.

[0032] Also described herein are methods for monitoring a folate receptor alpha (FRa)- expressing cancer in a subject. In some embodiments, the described methods involve exposing the biological sample of the subject to any one of the antibodies or antigen-binding fragments described herein. In some embodiments, the described methods involve exposing the biological sample of the subject to an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by the antibody or antigen binding fragment of any one of the antibodies or antigen-binding fragments described herein. In some embodiments, the described methods involve quantifying the amount of FRa present in the sample that is bound by the antibody or antigen-binding fragment. In some embodiments, the described methods involve comparing the amount of FRa present in the sample to a known standard. In some embodiments, the described methods involve comparing the amount of FRa present in the sample to a biological sample obtained from the subject at an earlier point in time. In some embodiments, the described methods involve determining whether the subject's FRa levels are indicative of cancer progression, regression or stable disease.

[0033] Also provided herein are methods for treating a folate receptor alpha (FRa)- expressing cancer in a subject. In some embodiments, the described methods involve exposing the biological sample of the subject to any one of the antibodies or antigen-binding fragments described herein. In some embodiments, the described methods involve exposing the biological sample of the subject to an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by any one of the antibodies or antigen-binding fragments described herein. In some embodiments, the described methods involve quantifying the amount of FRa present in the sample that is bound by the antibody or antigen-binding fragment. In some embodiments, the described methods involve comparing the amount of FRa present in the sample to a known standard. In some embodiments, the described methods involve determining whether the subject's FRa levels fall within the levels of FRa associated with cancer. In some embodiments, the described methods involve administering to the subject, or prescribing, a treatment for the cancer.

[0034] In some embodiments of the methods described herein, the antibody or antigen- binding fragment of any one of the antibodies or antigen-binding fragments described herein is labeled. In some embodiments, the label is a radiolabel, an epitope tag, biotin, a chromophore label, a fluorophore label, an electrochemiluminescence (ECL) label, or an enzyme. In preferred embodiments, the electrochemiluminescence (ECL) label is a sulfo-tag.

[0035] In some embodiments of the methods described herein, the antibody or antigen- binding fragment is the isolated antibody or antigen-binding fragment which includes a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method. In some embodiments of the methods described herein, the antibody or antigen-binding fragment is the isolated antibody or antigen-binding fragment which includes a light chain CDR1 amino acid sequence

substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method. In some embodiments, the FRa antibody is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 5, 2016 and assigned Accession No. PTA-123090. In some embodiments, the antibody or antigen-binding fragment is the isolated antibody or antigen-binding fragment with a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 31, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 32, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 33, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to SEQ ID NO: 35, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 36, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 37 or the isolated antibody or antigen-binding fragment produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 19, 2011 that has been assigned Accession No. PTA-11884.

[0036] In some embodiments of the methods described herein, the step of exposing a biological sample of the subject to the antibody or antigen-binding fragment of any one of the antibodies or antigen-binding fragments described herein or an antibody or antigen-binding fragment capable of binding the epitope of folate receptor alpha (FRa) that is bound by the antibody or antigen binding fragment of any one of the antibodies or antigen-binding fragments described herein further comprises exposing the biological sample of the subject to a second antibody or antigen-binding fragment capable of binding FRa.

[0037] In some embodiments of the methods described herein, the second antibody or antigen-binding fragment includes a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method. In some embodiments of the methods described herein, the second antibody or antigen-binding fragment includes a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method. In some embodiments of the methods described herein, the second antibody or antigen-binding fragment is the isolated antibody or antigen-binding fragment that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 5, 2016 that has been assigned Accession No. PTA-123090. In some embodiments, the second antibody or antigen-binding fragment is the isolated antibody or antigen-binding fragment with a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 31, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 32, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 33, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to SEQ ID NO: 35, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 36, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 37 or the isolated antibody or antigen-binding fragment that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 19, 2011 that has been assigned Accession No. PTA-11884.

[0038] In some embodiments, the antibody or antigen-binding fragment is the isolated antibody or antigen-binding fragment with a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 31, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 32, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 33, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to SEQ ID NO: 35, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 36, and a heavy chain

CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 37 or the isolated antibody or antigen-binding fragment that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va.

20110-2209) on May 19, 2011 that has been assigned Accession No. PTA-11884 and the second antibody or antigen-binding fragment is the isolated antibody or antigen-binding fragment with a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method; the isolated antibody or antigen-binding fragment with a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method; or the antigen-binding fragment is the isolated antibody or antigen-binding fragment that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 5, 2016 that has been assigned Accession No. PTA-123090.

[0039] In some embodiments, the second antibody or antigen-binding fragment is immobilized to a solid support. In some embodiments, the second antibody or antigen-binding fragment is biotinylated and the solid support is coated with streptavidin, and the isolated antibody or antigen-binding fragment is immobilized to the solid support by the binding of biotin to streptavidin. In some embodiments, the presence of folate receptor alpha (FRa) in the sample is detected using western blot, immunohistochemistry, immunofluorescence, flow cytometry, radioimmunoassay, immunoprecipitation, electrochemiluminescence immunoassay (ECLIA), or ELISA. In some embodiments, the FRa -expressing cancer is ovarian cancer. In some embodiments, the method is conducted following treatment of the subject for cancer with MORAb-003.

Kits of the Invention

[0040] Provided herein are kits for detecting the presence of folate receptor alpha (FRa) in a biological sample. In some embodiments, the kit may contain any one of the antibodies or antigen-binding fragments described herein. In some embodiments, the kit may contain an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by any one of the antibodies or antigen-binding fragments described herein. In some embodiments, the kit may contain an isolated antibody or antigen-binding fragment with a light chain CDR1 comprising the amino acid sequence of SEQ ID NO: 31, a light chain CDR2 comprising the amino acid sequence of SEQ ID NO: 32, a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 33, a heavy chain CDR1 comprising the amino acid sequence of SEQ ID NO: 35, a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 36, and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 37 or an isolated antibody or antigen- binding fragment that is produced by antibody -producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 19, 2011 that has been assigned Accession No. PTA-11884. In some embodiments, the kit may contain a vessel for containing the antibody, when not in use, and instructions for use of the antibody.

[0041] Also provided herein are kits for detecting the presence of folate receptor alpha (FRa) in a biological sample. In some embodiments, the kit may contain the antibody or antigen- binding fragment of any one of the antibodies or antigen-binding fragments described herein, wherein the antibody or antigen-binding fragment is affixed to a solid support. In some embodiments, the kit may contain an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by the antibody or antigen binding fragment of any one of the antibodies or antigen-binding fragments described herein wherein the antibody or antigen-binding fragment is affixed to a solid support. In some embodiments, the kit may contain an isolated antibody or antigen-binding fragment with a light chain CDR1 comprising the amino acid sequence of SEQ ID NO: 31, a light chain CDR2 comprising the amino acid sequence of SEQ ID NO: 32, a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 33, a heavy chain CDR1 comprising the amino acid sequence of SEQ ID NO: 35, a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 36, and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 37 or an isolated antibody or antigen-binding fragment that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 19, 2011 that has been assigned Accession No. PTA-11884, wherein the antibody or antigen-binding fragment is affixed to a solid support.

[0042] Also described herein are kits for detecting the presence of folate receptor alpha (FRa) in a biological sample. In some embodiments, the kit may contain the antibody or antigen- binding fragment of any one of the antibodies or antigen-binding fragments described herein, wherein the antibody or antigen-binding fragment is detectably labeled. In some embodiments, the kit may contain an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by the antibody or antigen binding fragment of any one of the antibodies or antigen-binding fragments described herein, wherein the antibody or antigen-binding fragment is detectably labeled. In some embodiments, the kit may contain an isolated antibody or antigen- binding fragment with a light chain CDR1 comprising the amino acid sequence of SEQ ID NO: 31, a light chain CDR2 comprising the amino acid sequence of SEQ ID NO: 32, a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 33, a heavy chain CDR1 comprising the amino acid sequence of SEQ ID NO: 35, a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 36, and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 37 or an isolated antibody or antigen-binding fragment that is produced by antibody- producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 19, 2011 that has been assigned Accession No. PTA-11884, wherein the antibody or antigen-binding fragment is detectably labeled.

BRIEF DESCRIPTION OF THE DRAWINGS

[0043] FIG. 1 depicts the migratory patterns of folate receptor alpha (FRa or FOLR1) by SDS-PAGE under nonreducing conditions. FRa was assessed in either native (lane 2) or reduced and alkylated (lane 3) form.

[0044] FIG. 2A shows the light intensity count resulting from pairwise combinations of thirteen capture antibodies and thirteen detection antibodies. FIG. 2B shows the average signal to background (S/B) values resulting from pairwise combinations of thirteen capture antibodies and thirteen detection antibodies.

[0045] FIG. 3A shows percent interference/drug suppression after adding 10μg/mL MORAb-003 for the pairwise combinations of thirteen capture antibodies and thirteen detection antibodies in a control calibrator solution containing untagged recombinant purified FRa at a concentration of 500pg/mL. FIG. 3B shows percent interference/drug suppression after adding 10μg/mL MORAb-003 for the pairwise combinations of thirteen capture antibodies and thirteen detection antibodies in serum samples. The positive control is located in the upper right corner for comparison. Percent interference = (Signal with MORAb-003 - Blank) / (Signal without MORAb-003 - Blank).

[0046] FIG. 4 shows examples of dilution linearity when using 24H8.D3 and 19D4.B7 as both the capture and detection antibody as compared to other antibody pairs. Dilution adjusted concentrations were normalized to the concentration at 1 :20 dilution and the grayed sections represent antibody combinations not considered during the screening. [0047] FIGS. 5A and 5B show the FRa standard curves and hillslopes. FIG. 5A depicts graphs of signal plotted against concentration for a defined capture antibody and paired with one of four detection antibodies. FIG. 5B shows the standard curve and hill slope data for the tested antibody pairs.

[0048] FIG. 6 shows a graph of light intensity counts of FRa standard samples across six consecutive runs plotted against the concentration (in pg/mL) of the standard samples.

[0049] FIGS. 7 A - 7D illustrate the FRa signal and FRa dilution linearity curves for five serum and five urine samples. FIG. 7A shows a graph of the light intensity counts (y-axis) of eight standard FRa samples and five serum samples (x-axis) at 10, 20, 40, 80, 160 and 320-fold dilutions. FIG. 7B shows a graph of the percent normalized recovery (y-axis) plotted against the fold dilution for all five serum samples (x-axis). FIG. 7C shows a graph of the light intensity counts (y-axis) of eight standard FRa samples and five urine samples (x-axis) at 10, 20, 40, 80, 160 and 320-fold dilutions. FIG. 7D shows a graph of the % normalized recovery (y-axis) plotted against the fold dilution for all five urine samples (x-axis).

[0050] FIGS. 8 A and 8B illustrate FRa serum and urine spike recovery values. Five serum samples and five urine samples were spiked with high (H), medium (M) and low (L) levels of FRa calibrator and run with a control diluent. The percent normalized recovery, as compared to expected recovery values, was plotted on the y-axis and spike levels were plotted on the x-axis. FIG. 8A shows the results from the five serum samples and FIG. 8B shows the results from the five urine samples.

[0051] FIG. 9 depicts percent coefficient of variance (CV) values for urine and serum/plasma samples, in duplicate.

[0052] FIG. 10A illustrates the percent inhibition of FRa levels in plasma and serum samples with and without 100μg/mL MORAb-003, where percent inhibition = (Diluent - MORAb-003) / Diluent. FIG. 10B is a plot of FRa levels in serum or plasma samples treated with 100μg/mL MORAb-003 (y-axis) against FRa levels in control, diluent-treated, serum or plasma samples (x-axis), and FIG. IOC is an expanded view of the low, boxed, end of the curve in FIG. 10B. R ² values for serum and plasma are also provided in FIG. IOC.

[0053] FIG. 11 shows a graph of the FRa light intensity count (y-axis) for eight standard samples, serum and plasma samples with and without MORAb-003, and spot and AM urine samples (x-axis).

[0054] FIGS. 12A and 12B show the antibody characterization profiles for 24H8.D3 (FIG. 12A) and 19D4.B7 (FIG. 12B), along with the results from capillary isoelectric focusing (cIEF), dynamic light scattering (DLS), and experion automated electrophoresis characterization tests.

DETAILED DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS

[0055] The following description characterizes antibodies that specifically bind to FRa. Also described are related polynucleotides capable of encoding the provided antibodies, cells expressing the provided antibodies, as well as associated vectors and detectable antibody labels. In addition, methods of using the provided antibodies to detect FRa and to diagnose, monitor, or treat ovarian cancer are described. For example, the provided antibodies may be used to diagnose, monitor or treat a folate receptor alpha-expressing cancer in a subject.

Definitions

[0056] Various terms relating to aspects of the description are used throughout the specification and claims. Such terms are to be given their ordinary meaning in the art unless otherwise indicated. Other specifically defined terms are to be construed in a manner consistent with the definitions provided herein.

[0057] As used in this specification and the appended claims, the singular forms "a," "an," and "the" include plural referents unless the content clearly dictates otherwise. Thus, for example, reference to "a cell" includes a combination of two or more cells, and the like.

[0058] The term "about" as used herein when referring to a measurable value such as an amount, a temporal duration, and the like, is meant to encompass variations of up to ±10% from the specified value; as such variations are appropriate to perform the disclosed methods. Unless otherwise indicated, all numbers expressing quantities of ingredients, properties such as molecular weight, reaction conditions, and so forth used in the specification and claims are to be understood as being modified in all instances by the term "about." Accordingly, unless indicated to the contrary, the numerical parameters set forth in the following specification and attached claims are approximations that may vary depending upon the desired properties sought to be obtained by the present invention. At the very least, and not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims, each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques.

[0059] Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contain certain errors necessarily resulting from the standard deviation found in their respective testing measurements.

[0060] "Isolated" means a biological component (such as a nucleic acid, peptide or protein) has been substantially separated, produced apart from, or purified away from other biological components of the organism in which the component naturally occurs, i.e., other chromosomal and extrachromosomal DNA and RNA, and proteins. Nucleic acids, peptides and proteins that have been "isolated" thus include nucleic acids and proteins purified by standard purification methods. "Isolated" nucleic acids, peptides and proteins that can be part of a composition and still be isolated if such composition is not part of the native environment of the nucleic acid, peptide, or protein. The term also embraces nucleic acids, peptides and proteins prepared by recombinant expression in a host cell as well as chemically synthesized nucleic acids.

[0061] "Polynucleotide," synonymously referred to as "nucleic acid molecule" or "nucleic acids," refers to any polyribonucleotide or polydeoxyribonucleotide, which may be unmodified RNA or DNA or modified RNA or DNA. "Polynucleotides" include, without limitation single- and double-stranded DNA, DNA that is a mixture of single- and double- stranded regions, single- and double-stranded RNA, and RNA that is mixture of single- and double-stranded regions, hybrid molecules comprising DNA and RNA that may be single- stranded or, more typically, double-stranded or a mixture of single- and double-stranded regions. In addition, "polynucleotide" refers to triple-stranded regions comprising RNA or DNA or both RNA and DNA. The term polynucleotide also includes DNAs or RNAs containing one or more modified bases and DNAs or RNAs with backbones modified for stability or for other reasons. "Modified" bases include, for example, tritylated bases and unusual bases such as inosine. A variety of modifications may be made to DNA and RNA; thus, "polynucleotide" embraces chemically, enzymatically or metabolically modified forms of polynucleotides as typically found in nature, as well as the chemical forms of DNA and RNA characteristic of viruses and cells. "Polynucleotide" also embraces relatively short nucleic acid chains, often referred to as oligonucleotides.

[0062] The meaning of "substantially the same" can differ depending on the context in which the term is used. Because of the natural sequence variation likely to exist among heavy and light chains and the genes encoding them, one would expect to find some level of variation within the amino acid sequences or the genes encoding the antibodies or antigen-binding fragments described herein, with little or no impact on their unique binding properties (e.g., specificity and affinity). Such an expectation is due in part to the degeneracy of the genetic code, as well as to the evolutionary success of conservative amino acid sequence variations, which do not appreciably alter the nature of the encoded protein. Accordingly, in the context of nucleic acid sequences, "substantially the same" means at least 65% identity between two or more sequences. Preferably, the term refers to at least 70% identity between two or more sequences, more preferably at least 75% identity, more preferably at least 80% identity, more preferably at least 85% identity, more preferably at least 90% identity, more preferably at least 91% identity, more preferably at least 92% identity, more preferably at least 93% identity, more preferably at least 94% identity, more preferably at least 95% identity, more preferably at least 96% identity, more preferably at least 97% identity, more preferably at least 98% identity, and more preferably at least 99% or greater identity. Such identity may be determined using nBLAST algorithm (Altschul et al., (1990) Proc. Natl. Acad. Sci. USA 87:2264-8; Karlin and Altschul (1993) Proc. Natl. Acad. Sci. USA 90:5873- 7).

[0063] The degree of variation that may occur within the amino acid sequence of a protein without having a substantial effect on protein function is much lower than that of a nucleic acid sequence, since the same degeneracy principles do not apply to amino acid sequences.

Accordingly, in the context of an antibody or antigen-binding fragment, "substantially the same" means antibodies or antigen-binding fragments having 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identity to the antibodies or antigen-binding fragments described. Other embodiments include FRa specific antibodies, or antigen-binding fragments, that have framework, scaffold, or other non-binding regions that do not share significant identity with the antibodies and antigen-binding fragments described herein, but do incorporate one or more CDRs or other sequences needed to confer binding that are 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to such sequences described herein.

[0064] A "vector" is a replicon, such as plasmid, phage, cosmid, or virus in which another nucleic acid segment may be operably inserted so as to bring about the replication or expression of the segment.

[0065] A cell has been "transformed" when exogenous or heterologous nucleic acids such as DNA have been introduced inside the cell. The transforming DNA may or may not be integrated (covalently linked) into the genome of the cell. In prokaryotes, yeast, and mammalian cells for example, the transforming DNA may be maintained on an episomal element such as a plasmid. With respect to eukaryotic cells, a stably transformed cell, or "stable cell" is

demonstrated by the ability of the eukaryotic cell to establish cell lines or clones comprised of a population of daughter cells containing the transforming DNA. A "clone" is a population of cells derived from a single cell or common ancestor by mitosis. A "cell line" is a clone of a primary cell that is capable of stable growth in vitro for many generations. In some examples provided herein, cells are transformed by transfecting the cells with DNA.

[0066] The terms "express" and "produce" are used synonymously herein, and refer to the biosynthesis of a gene product. These terms encompass the transcription of a gene into RNA. These terms also encompass translation of RNA into one or more polypeptides, and further encompass all naturally occurring post-transcriptional and post-translational modifications. The expression or production of an antibody or antigen-binding fragment thereof may be within the cytoplasm of the cell, or into the extracellular milieu such as the growth medium of a cell culture.

[0067] The terms "treating" or "treatment" refer to any success or indicia of success in the attenuation or amelioration of an injury, pathology or condition, including any objective or subjective parameter such as abatement, remission, diminishing of symptoms or making the condition more tolerable to the patient, slowing in the rate of degeneration or decline, making the final point of degeneration less debilitating, improving a subject's physical or mental well-being, or prolonging the length of survival. The treatment may be assessed by objective or subjective parameters; including the results of a physical examination, neurological examination, or psychiatric evaluations.

[0068] "Antibody" refers to all isotypes of immunoglobulins (IgG, IgA, IgE, IgM, IgD, and IgY) including various monomeric and polymeric forms of each isotype, unless otherwise specified.

[0069] Antigen-binding fragments are any proteinaceous structure that may exhibit binding affinity for a particular antigen. Some antigen-binding fragments are composed of portions of intact antibodies that retain antigen-binding specificity of the parent antibody molecule. For example, antigen-binding fragments may comprise at least one variable region (either a heavy chain or light chain variable region) or one or more CDRs of an antibody known to bind a particular antigen. Examples of suitable antigen-binding fragments include, without limitation diabodies and single-chain molecules as well as Fab, F(ab')2, Fc, Fabc, and Fv molecules, single chain (Sc) antibodies, individual antibody light chains, individual antibody heavy chains, chimeric fusions between antibody chains or CDRs and other proteins, protein scaffolds, heavy chain monomers or dimers, light chain monomers or dimers, dimers consisting of one heavy and one light chain, and the like. All antibody isotypes may be used to produce antigen-binding fragments. Additionally, antigen-binding fragments may include non-antibody proteinaceous frameworks that may successfully incorporate polypeptide segments in an orientation that confers affinity for a given antigen of interest, such as protein scaffolds. Antigen- binding fragments may be recombinantly produced or produced by enzymatic or chemical cleavage of intact antibodies. The phrase "an antibody or antigen-binding fragment thereof may be used to denote that a given antigen-binding fragment incorporates one or more amino acid segments of the antibody referred to in the phrase. The CDR sequences of this invention are defined using the KABAT method (Kabat, E. A. et al, Sequences of Proteins of Immunological Interest, Fifth Edition, U.S. Department of Health and Human Services, U.S. Government Printing Office (1991)) or the international ImMunoGeneTics (IMGT) method (Lefranc, M.-P., et al. (2005). IMGT, the international ImMunoGeneTics information system®. Nucl. Acids Res. 33, D593-D597).

[0070] "Specific binding" when used in the context of antibodies, or antibody fragments, represents binding via domains encoded by immunoglobulin genes or fragments of immunoglobulin genes to one or more epitopes of a protein of interest, but which do not substantially recognize and bind other molecules in a sample containing a mixed population of antigenic molecules. Typically, an antibody binds to a cognate antigen with a Kd of less than about 1 x 10 ^"8 M, as measured by a surface plasmon resonance assay or a cell binding assay.

[0071] The term "subject" refers to human and non-human animals, including all vertebrates, e.g., mammals and non-mammals, such as non-human primates, mice, rabbits, sheep, dogs, cats, horses, cows, chickens, amphibians, and reptiles. In many embodiments of the described methods, the subject is a human.

[0072] As used herein, the term "folate receptor alpha" (also referred to as FRa, FR- alpha, FOLR-1 or FOLR1) refers to the alpha isoform of the high affinity receptor for folate. Membrane bound FRa is attached to the cell surface by a glycosyl phosphatidylinositol (GPI) anchor. Soluble forms of FRa may be derived by the action of proteases or phospholipase on membrane anchored folate receptors. The amino acid sequence for human FRa is set forth herein as SEQ ID NO: 293. Variants, for example, naturally occurring allelic variants or sequences containing at least one amino acid substitution, are encompassed by the terms as used herein. As will be appreciated by those skilled in the art, cell associated and non-cell associated forms of human FRa may encompass variant forms of SEQ ID NO: 293.

[0073] The term "sample" as used herein refers to a collection of similar fluids, cells, or tissues (e.g., surgically resected tumor tissue, biopsies, including fine needle aspiration), isolated from a subject, as well as fluids, cells, or tissues present within a subject. In some embodiments the sample is a biological fluid. Biological fluids are typically liquids at physiological temperatures and may include naturally occurring fluids present in, withdrawn from, expressed or otherwise extracted from a subject or biological source. Certain biological fluids derive from particular tissues, organs or localized regions and certain other biological fluids may be more globally or systemically situated in a subject or biological source. Examples of biological fluids include blood, serum and serosal fluids, plasma, lymph, urine, saliva, cystic fluid, tear drops, feces, sputum, mucosal secretions of the secretory tissues and organs, vaginal secretions, ascites fluids such as those associated with non-solid tumors, fluids of the pleural, pericardial, peritoneal, abdominal and other body cavities, fluids collected by bronchial lavage and the like.

[0074] Biological fluids may also include liquid solutions contacted with a subject or biological source, for example, cell and organ culture medium including cell or organ conditioned medium, lavage fluids and the like. The term "sample," as used herein, encompasses materials removed from a subject or materials present in a subject.

[0075] The term "progression," as used in the context of progression of a FRa- expressing cancer, includes the change of a cancer from a less severe to a more severe state. This could include an increase in the number or severity of tumors, the degree of metastasis, the speed with which the cancer is growing or spreading, and the like. For example, "the progression of ovarian cancer" includes the progression of such a cancer from a less severe to a more severe state, such as the progression from stage I to stage II, from stage II to stage III, etc.

[0076] The term "regression," as used in the context of regression of a FRa-expressing cancer, includes the change of a cancer from a more severe to a less severe state. This could include a decrease in the number or severity of tumors, the degree of metastasis, the speed with which the cancer is growing or spreading, and the like. For example, "the regression of ovarian cancer" includes the regression of such a cancer from a more severe to a less severe state, such as the progression from stage III to stage II, from stage II to stage I, etc.

[0077] The term "stable" as used in the context of stable FRa-expressing cancer, is intended to describe a disease condition that is not, or has not, changed significantly enough over a clinically relevant period of time to be considered a progressing cancer or a regressing cancer.

[0078] The embodiments described herein are not limited to particular methods, reagents, compounds, compositions or biological systems, which can, of course, vary.

FRa-Speciflc Antibodies and Antigen-Binding Fragments

[0079] Described herein are isolated monoclonal antibodies or antigen-binding fragments that specifically bind FRa. The general structure of an antibody molecule comprises an antigen binding domain, which includes heavy and light chains, and the Fc domain, which serves a variety of functions, including complement fixation and binding antibody receptors.

[0080] The described antibodies or antigen-binding fragments include all isotypes, IgA,

IgD, IgE, IgG and IgM, and synthetic multimers of the four-chain immunoglobulin structure. The described antibodies or antigen-binding fragments also include the IgY isotype generally found in hen or turkey serum and hen or turkey egg yolk.

[0081] The antibodies or antigen-binding fragments described herein can occur in a variety of forms, but will include one or more of the antibody variable domain segments or CDRs shown in Table 1.

Table 1: Antibody segments of the described anti-FRa antibodies and antigen-binding fragments thereof ("Lc" denotes light chain and "He" denotes heavy chain)

[0082] Described herein are isolated antibodies and antigen-binding fragments that specifically bind to FRa. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, wherein the CDRs are defined according to the IMGT method. In some embodiments, the antibodies or antigen- binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 9, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 10, wherein the CDR is defined according to the IMGT method.

[0083] In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 12, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 13, wherein the CDR is defined according to the KABAT method.

[0084] Described herein are isolated antibodies and antigen-binding fragments that specifically bind to FRa. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ

ID NO: 55, a light chain CDR2 amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 56, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 62, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 63, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 64, wherein the CDRs are defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 55. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 56, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 62, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 63, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 64, wherein the CDR is defined according to the IMGT method.

[0085] In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 58, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 59, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 65, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 66, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 64, wherein the CDRs are defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 58, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen- binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 59, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 65, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 66, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 64, wherein the CDR is defined according to the KABAT method.

[0086] Described herein are isolated antibodies and antigen-binding fragments that specifically bind to FRa. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 84, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 85, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 86, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 90, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 91, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 92, wherein the CDRs are defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 84. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 85, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 86, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 90, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 91, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 92, wherein the CDR is defined according to the IMGT method. [0087] In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 87, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 32, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 86, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 93, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 94, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 95, wherein the CDRs are defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 87, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen- binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 32, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 86, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 93, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 94, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 95, wherein the CDR is defined according to the KABAT method.

[0088] Described herein are isolated antibodies and antigen-binding fragments that specifically bind to FRa. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ

ID NO: 112, a light chain CDR2 amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 113, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 118, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 119, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 120, wherein the CDRs are defined according to the

IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 112. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen- binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 113, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 118, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 119, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 120, wherein the CDR is defined according to the IMGT method.

[0089] In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 114, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 115, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 113, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 121, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 122, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 123, wherein the CDRs are defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 114, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 115, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 113, wherein the CDR is defined according to the KABAT method. In some

embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 121, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 122, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 123, wherein the CDR is defined according to the KABAT method.

[0090] Described herein are isolated antibodies and antigen-binding fragments that specifically bind to FRa. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 55, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 140, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 141, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 145, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 146, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 147, wherein the CDRs are defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 55. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 140, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen- binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 141, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 145, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 146, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 147, wherein the CDR is defined according to the IMGT method.

[0091] In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 58, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO:

142, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID

NO: 141, a heavy chain CDRl amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 148, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 149, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 150, wherein the CDRs are defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 58, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 142, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 141, wherein the CDR is defined according to the KABAT method. In some

embodiments, the antibodies or antigen-binding fragments include a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 148, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 149, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 150, wherein the CDR is defined according to the KABAT method.

[0092] Described herein are isolated antibodies and antigen-binding fragments that specifically bind to FRa. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 55, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 56, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 168, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 169, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 170, wherein the CDRs are defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 55. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 56, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen- binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 168, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 169, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 170, wherein the CDR is defined according to the IMGT method.

[0093] In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 58, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 59, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 171, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 172, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 173, wherein the CDRs are defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 58, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen- binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 59, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 171, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 172, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 173, wherein the CDR is defined according to the KABAT method.

[0094] Described herein are isolated antibodies and antigen-binding fragments that specifically bind to FRa. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 187, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 188, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 194, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 195, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 196, wherein the CDRs are defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 187. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 188, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen- binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 194, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 195, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 196, wherein the CDR is defined according to the IMGT method.

[0095] In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 190, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 191, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 197, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 198, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 199, wherein the CDRs are defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 190, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 191, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, wherein the CDR is defined according to the KABAT method. In some

embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 197, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 198, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 199, wherein the CDR is defined according to the KABAT method.

[0096] Described herein are isolated antibodies and antigen-binding fragments that specifically bind to FRa. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 217, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 188, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 194, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 221, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 196, wherein the CDRs are defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 217. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 188, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen- binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 194, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 221, wherein the CDR is defined according to the IMGT method.

In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 196, wherein the CDR is defined according to the IMGT method.

[0097] In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 218, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 191, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 197, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 222, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 199, wherein the CDRs are defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 218, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 191, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, wherein the CDR is defined according to the KABAT method. In some

embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 197, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 222, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 199, wherein the CDR is defined according to the KABAT method.

[0098] Described herein are isolated antibodies and antigen-binding fragments that specifically bind to FRa. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ

ID NO: 233, a light chain CDR2 amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 234, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 235, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 194, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 195, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 240, wherein the CDRs are defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 233. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 234, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen- binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 235, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 194, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 195, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 240, wherein the CDR is defined according to the IMGT method.

[0099] In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 236, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 237, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 235, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 241, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 198, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 242, wherein the CDRs are defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 236, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 237, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 235, wherein the CDR is defined according to the KABAT method. In some

embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 241, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 198, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 242, wherein the CDR is defined according to the KABAT method.

[00100] Described herein are isolated antibodies and antigen-binding fragments that specifically bind to FRa. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 257, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 188, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 258, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 262, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 263, wherein the CDRs are defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 257. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 188, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 258, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 262, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 263, wherein the CDR is defined according to the IMGT method.

[00101] In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO:

259, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID

NO: 191, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 258, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 264, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 265, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 266, wherein the CDRs are defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 259, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 191, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 258, wherein the CDR is defined according to the KABAT method. In some

embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 264, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 265, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 266, wherein the CDR is defined according to the KABAT method.

[00102] Described herein are isolated antibodies and antigen-binding fragments that specifically bind to FRa. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen- binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 9, wherein the CDR is defined according to the IMGT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 10, wherein the CDR is defined according to the IMGT method.

[00103] In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 115, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen- binding fragments include a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 115, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen- binding fragments include a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR2 substantially the same as, or identical to, amino acid sequence of SEQ ID NO: 12, wherein the CDR is defined according to the KABAT method. In some embodiments, the antibodies or antigen-binding fragments include a heavy chain CDR3 amino acid sequence substantially the same as, or identical to SEQ ID NO: 13, wherein the CDR is defined according to the KABAT method. [00104] The antibodies or antigen-binding fragments disclosed in the examples section are derived from mice. Similar antibodies may be derived from any species by recombinant means. For example, the antibodies or antigen-binding fragments may be chimeric rat, goat, horse, swine, bovine, chicken, rabbit, camelid, donkey, human, and the like. For use in administration to humans, non-human derived antibodies or antigen-binding fragments may be genetically or structurally altered to be less antigenic upon administration to a human patient.

[00105] In some embodiments, the antibodies or antigen-binding fragments are chimeric. As used herein, the term "chimeric" refers to an antibody, or antigen-binding fragment thereof, having at least some portion of at least one variable domain derived from the antibody amino acid sequence of a non-human mammal, a rodent, or a reptile, while the remaining portions of the antibody, or antigen-binding fragment thereof, are derived from a human. For example, a chimeric antibody may comprise a mouse antigen binding domain with a human Fc or other such structural domain.

[00106] In some embodiments, the antibodies are humanized antibodies. Humanized antibodies may be chimeric immunoglobulins, immunoglobulin chains or fragments thereof (such as Fv, Fab, Fab', F(ab')2 or other antigen-binding subsequences of antibodies) that contain minimal sequence derived from non-human immunoglobulin. For the most part, humanized antibodies are human immunoglobulins (recipient antibody) in which residues from a

complementary-determining region (CDR) of the recipient are replaced by residues from a CDR of a non-human species (donor antibody) such as mouse, rat or rabbit having the desired specificity, affinity, and capacity. In general, the humanized antibody will comprise substantially all of at least one, and typically two, variable domains, in which all or substantially all of the CDR regions correspond to those of a non-human immunoglobulin and all or substantially all of the framework regions are those of a human immunoglobulin sequence. The humanized antibody may include at least a portion of an immunoglobulin constant region (Fc), typically that of a human immunoglobulin.

[00107] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 6 and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 14 where the antibodies or antigen- binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method.

[00108] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 6, and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 14 where the antibodies or antigen- binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method.

[00109] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 47 and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 49 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method.

[00110] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 47, and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 49 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method.

[00111] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 60 and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 67 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 55, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 56, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 62, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 63, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 64, wherein the CDRs are defined according to the IMGT method.

[00112] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 60, and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 67 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 58, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 59, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 65, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 66, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 64, wherein the CDRs are defined according to the KABAT method.

[00113] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 88 and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 96 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 84, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 85, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 86, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 90, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 91, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 92, wherein the CDRs are defined according to the IMGT method.

[00114] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 88, and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 96 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 87, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 32, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 86, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 93, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 94, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 95, wherein the CDRs are defined according to the KABAT method.

[00115] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 116 and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 124 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 112, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 113, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 118, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 119, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 120, wherein the CDRs are defined according to the IMGT method.

[00116] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 116, and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 124 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 114, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 115, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 113, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 121, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 122, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 123, wherein the CDRs are defined according to the KABAT method.

[00117] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 143 and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 151 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 55, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 140, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 141, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 145, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 146, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 147, wherein the CDRs are defined according to the IMGT method.

[00118] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 143, and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 151 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 58, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 142, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 141, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 148, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 149, and a heavy chain

CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 150, wherein the CDRs are defined according to the KABAT method. [00119] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 166 and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 174 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 55, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 56, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 168, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 169, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 170, wherein the CDRs are defined according to the IMGT method.

[00120] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 166, and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 174 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 58, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 59, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 171, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 172, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 173, wherein the CDRs are defined according to the KABAT method.

[00121] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 192 and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 200 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 187, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 188, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 194, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 195, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 196, wherein the CDRs are defined according to the IMGT method.

[00122] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 192, and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 200 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 190, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 191, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 197, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 198, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 199, wherein the CDRs are defined according to the KABAT method.

[00123] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 219 and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 223 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 217, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 188, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 194, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 221, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 196, wherein the CDRs are defined according to the IMGT method.

[00124] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 219, and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 223 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 218, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 191, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 197, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 222, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 199, wherein the CDRs are defined according to the KABAT method.

[00125] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 238 and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 243 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 233, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 234, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 235, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 194, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 195, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 240, wherein the CDRs are defined according to the IMGT method.

[00126] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 238, and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 243 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 236, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 237, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 235, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 241, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 198, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 242, wherein the CDRs are defined according to the KABAT method.

[00127] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 260 and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 267 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 257, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 188, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 258, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 262, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 263, wherein the CDRs are defined according to the IMGT method.

[00128] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 260, and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 267 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 259, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 191, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 258, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 264, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 265, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 266, wherein the CDRs are defined according to the KABAT method.

[00129] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 282 and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 284 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method.

[00130] Also disclosed are antibodies or antigen-binding fragments comprising a light chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 282, and a heavy chain variable region amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 284 where the antibodies or antigen-binding fragments include a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 115, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method.

[00131] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 6. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 14. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 6 and a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 14.

[00132] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 7. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 15. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 7 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 15.

[00133] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 47. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 49. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 47 and a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 49.

[00134] Also disclosed are isolated antibodies or antigen-binding fragments specific for

FRa which include a light chain amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 48. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 50. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 48 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 50.

[00135] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 60. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 67. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 60 and a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 67.

[00136] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 61. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 68. In some embodiments, the isolated antibodies or antigen-binding fragments include a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 61 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 68.

[00137] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 88. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 96. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 88 and a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 96.

[00138] Also disclosed are isolated antibodies or antigen-binding fragments specific for

FRa which include a light chain amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 89. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID

NO: 97. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 89 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 97. [00139] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 116. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 124. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 116 and a heavy chain variable region amino acid sequence

substantially the same as, or identical to, SEQ ID NO: 124.

[00140] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 117. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 125. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 117 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 125.

[00141] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 143. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 151. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 143 and a heavy chain variable region amino acid sequence

substantially the same as, or identical to, SEQ ID NO: 151.

[00142] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 144. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 152. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 144 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 152.

[00143] Also disclosed are isolated antibodies or antigen-binding fragments specific for

FRa which include a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 166. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 174. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 166 and a heavy chain variable region amino acid sequence

substantially the same as, or identical to, SEQ ID NO: 174.

[00144] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa may include a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 167. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 175. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 167 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 175.

[00145] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 192. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 200. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 192 and a heavy chain variable region amino acid sequence

substantially the same as, or identical to, SEQ ID NO: 200.

[00146] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 193. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 201. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 193 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 201.

[00147] Also disclosed are isolated antibodies or antigen-binding fragments specific for

FRa which include a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 219. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 223. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 219 and a heavy chain variable region amino acid sequence

substantially the same as, or identical to, SEQ ID NO: 223. [00148] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 220. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 224. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 220 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 224.

[00149] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 238. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 243. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 238 and a heavy chain variable region amino acid sequence

substantially the same as, or identical to, SEQ ID NO: 243.

[00150] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 239. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 244. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 239 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 244.

[00151] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 260. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 267. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 260 and a heavy chain variable region amino acid sequence

substantially the same as, or identical to, SEQ ID NO: 267.

[00152] Also disclosed are isolated antibodies or antigen-binding fragments specific for

FRa which include a light chain amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 261. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 268. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 261 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 268.

[00153] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 282. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 284. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain variable region amino acid sequence substantially the same as, or identical to, SEQ ID NO: 282 and a heavy chain variable region amino acid sequence

substantially the same as, or identical to, SEQ ID NO: 284.

[00154] Also disclosed are isolated antibodies or antigen-binding fragments specific for FRa which include a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 283. In some embodiments, the isolated antibody or antigen-binding fragment includes a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 285. In some embodiments, the isolated antibody or antigen-binding fragment includes a light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 283 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 285.

[00155] In some embodiments, the FRa antibody is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas,

Va. 20110-2209) on May 5, 2016 and assigned Accession No. PTA-123090. In some

embodiments, the FRa antibody is produced by antibody-producing cells deposited with the

American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May

4, 2016 and assigned Accession No. PTA-123097. In some embodiments, the FRa antibody is produced by antibody-producing cells deposited with the American Type Culture Collection

(10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 and assigned Accession

No. PTA-123091. In some embodiments, the FRa antibody is produced by antibody -producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas,

Va. 20110-2209) on May 4, 2016 and assigned Accession No. PTA-123098. In some

embodiments, the FRa antibody is produced by antibody-producing cells deposited with the

American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May

4, 2016 and assigned Accession No. PTA-123093. In some embodiments, the FRa antibody is produced by antibody-producing cells deposited with the American Type Culture Collection

(10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 and assigned Accession No. PTA-123094. In some embodiments, the FRa antibody is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 and assigned Accession No. PTA-123092. In some embodiments, the FRa antibody is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 and assigned Accession No. PTA-123098. In some embodiments, the FRa antibody is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 and assigned Accession No. PTA-123095. In some embodiments, the FRa antibody is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 and assigned Accession No. PTA-123101. In some embodiments, the FRa antibody is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 and assigned Accession No. PTA-123096. In some embodiments, the FRa antibody is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 and assigned Accession No. PTA-123100. In some embodiments, the antibodies, or antigen-binding fragments thereof, have the binding affinity for FRa of the antibodies produced by the deposited antibody -producing cells. In some embodiments, the disclosed antibodies, or antigen-binding fragments thereof, comprise the light and heavy chain CDRs of the antibodies produced by the deposited antibody- producing cells. In some embodiments, the antibodies, or antigen-binding fragments thereof, comprise the light and heavy chain variable regions of the antibodies produced by the deposited antibody-producing cells.

[00156] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 21. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 29. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 21 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 29.

[00157] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 22. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 30. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 22 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 30.

[00158] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 51. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 53. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 51 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 53.

[00159] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 52. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 54. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 52 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 54.

[00160] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 74. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 82. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 74 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 82.

[00161] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 75. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 83. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 75 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 83.

[00162] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 102. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 110. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 102 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 110.

[00163] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 103. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 111. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 103 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 111.

[00164] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 130. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 138. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 130 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 138.

[00165] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 131. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 139. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 131 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 139.

[00166] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 156. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 164. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 156 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 164.

[00167] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 157. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 165. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 157 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 165.

[00168] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 177. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID

NO: 185. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 177 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 185. [00169] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 178. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 186. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 178 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 186.

[00170] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 207. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 215. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 207 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 215.

[00171] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 208. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 216. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 208 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 216.

[00172] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 227. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 231. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 227 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 231.

[00173] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 228. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 232. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 228 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 232.

[00174] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 250. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID

NO: 255. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 250 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 255.

[00175] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 251. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 256. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 251 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 256.

[00176] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 272. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 280. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 272 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 280.

[00177] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 273. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 281. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 273 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 281.

[00178] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 286. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 291. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 286 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 291.

[00179] Also disclosed are isolated polynucleotides which have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 287. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 292. In some embodiments, the isolated polynucleotides have a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 287 and a nucleotide sequence substantially the same as, or identical to, SEQ ID NO: 292.

[00180] Also disclosed are isolated polynucleotides that encode an antibody or antigen- binding fragment comprising a light chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 6. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a heavy chain variable region, wherein the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 14. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a light chain variable region and a heavy chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 6 and the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 14.

[00181] Also disclosed are isolated polynucleotides that encode an antibody comprising a light chain, wherein the light chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 7. In some embodiments, the isolated polynucleotides encode an antibody comprising a heavy chain, wherein the heavy chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 15. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a light chain and a heavy chain, wherein the light chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 7 and the heavy chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 15.

[00182] Also disclosed are isolated polynucleotides that encode an antibody or antigen- binding fragment comprising a light chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 47. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a heavy chain variable region, wherein the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 49. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a light chain variable region and a heavy chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 47 and the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 49.

[00183] Also disclosed are isolated polynucleotides that encode an antibody comprising a light chain, wherein the light chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 48. In some embodiments, the isolated polynucleotides encode an antibody comprising a heavy chain, wherein the heavy chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 50. In some embodiments, the isolated polynucleotides encode an antibody comprising a light chain and a heavy chain, wherein the light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 48 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 50.

[00184] Also disclosed are isolated polynucleotides that encode an antibody or antigen- binding fragment comprising a light chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 60. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a heavy chain variable region, wherein the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 67. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a light chain variable region and a heavy chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 60 and the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 67.

[00185] Also disclosed are isolated polynucleotides that encode an antibody comprising a light chain, wherein the light chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 61. In some embodiments, the isolated polynucleotides encode an antibody comprising a heavy chain, wherein the heavy chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 68. In some embodiments, the isolated polynucleotides encode an antibody comprising a light chain and a heavy chain, wherein the light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 61 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 68.

[00186] Also disclosed are isolated polynucleotides that encode an antibody or antigen- binding fragment comprising a light chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 88. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a heavy chain variable region, wherein the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 96. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a light chain variable region and a heavy chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 88 and the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 96.

[00187] Also disclosed are isolated polynucleotides that encode an antibody comprising a light chain, wherein the light chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 89. In some embodiments, the isolated polynucleotides encode an antibody comprising a heavy chain, wherein the heavy chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 97. In some embodiments, the isolated polynucleotides encode an antibody comprising a light chain and a heavy chain, wherein the light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 89 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 97.

[00188] Also disclosed are isolated polynucleotides that encode an antibody or antigen- binding fragment comprising a light chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 116. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a heavy chain variable region, wherein the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 124. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a light chain variable region and a heavy chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 116 and the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 124.

[00189] Also disclosed are isolated polynucleotides that encode an antibody comprising a light chain, wherein the light chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 117. In some embodiments, the isolated polynucleotides encode an antibody comprising a heavy chain, wherein the heavy chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 125. In some embodiments, the isolated polynucleotides encode an antibody comprising a light chain and a heavy chain, wherein the light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 117 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 125.

[00190] Also disclosed are isolated polynucleotides that encode an antibody or antigen- binding fragment comprising a light chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 143. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a heavy chain variable region, wherein the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 151. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a light chain variable region and a heavy chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 143 and the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 151. [00191] Also disclosed are isolated polynucleotides that encode an antibody comprising a light chain, wherein the light chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 144. In some embodiments, the isolated polynucleotides encode an antibody comprising a heavy chain, wherein the heavy chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 152. In some embodiments, the isolated polynucleotides encode an antibody comprising a light chain and a heavy chain, wherein the light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 144 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 152.

[00192] Also disclosed are isolated polynucleotides that encode an antibody or antigen- binding fragment comprising a light chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 166. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a heavy chain variable region, wherein the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 174. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a light chain variable region and a heavy chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 166 and the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 174.

[00193] Also disclosed are isolated polynucleotides that encode an antibody comprising a light chain, wherein the light chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 167. In some embodiments, the isolated polynucleotides encode an antibody comprising a heavy chain, wherein the heavy chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 175. In some embodiments, the isolated polynucleotides encode an antibody comprising a light chain and a heavy chain, wherein the light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 167 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 175.

[00194] Also disclosed are isolated polynucleotides that encode an antibody or antigen- binding fragment comprising a light chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 192. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a heavy chain variable region, wherein the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 200. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a light chain variable region and a heavy chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 192 and the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 200.

[00195] Also disclosed are isolated polynucleotides that encode an antibody comprising a light chain, wherein the light chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 193. In some embodiments, the isolated polynucleotides encode an antibody comprising a heavy chain, wherein the heavy chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 201. In some embodiments, the isolated polynucleotides encode an antibody comprising a light chain and a heavy chain, wherein the light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 193 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 201.

[00196] Also disclosed are isolated polynucleotides that encode an antibody or antigen- binding fragment comprising a light chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 219. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a heavy chain variable region, wherein the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 223. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a light chain variable region and a heavy chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 219 and the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 223.

[00197] Also disclosed are isolated polynucleotides that encode an antibody comprising a light chain, wherein the light chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 220. In some embodiments, the isolated polynucleotides encode an antibody comprising a heavy chain, wherein the heavy chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 224. In some embodiments, the isolated polynucleotides encode an antibody comprising a light chain and a heavy chain, wherein the light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 220 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 224.

[00198] Also disclosed are isolated polynucleotides that encode an antibody or antigen- binding fragment comprising a light chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 238. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a heavy chain variable region, wherein the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 243. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a light chain variable region and a heavy chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 238 and the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 243.

[00199] Also disclosed are isolated polynucleotides that encode an antibody comprising a light chain, wherein the light chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 239. In some embodiments, the isolated polynucleotides encode an antibody comprising a heavy chain, wherein the heavy chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 244. In some embodiments, the isolated polynucleotides encode antibody comprising a light chain and a heavy chain, wherein the light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 239 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 244.

[00200] Also disclosed are isolated polynucleotides that encode an antibody or antigen- binding fragment comprising a light chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 260. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a heavy chain variable region, wherein the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 267. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a light chain variable region and a heavy chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 260 and the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 267.

[00201] Also disclosed are isolated polynucleotides that encode an antibody comprising a light chain, wherein the light chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 261. In some embodiments, the isolated polynucleotides encode an antibody comprising a heavy chain, wherein the heavy chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 268. In some embodiments, the isolated polynucleotides encode an antibody comprising a light chain and a heavy chain, wherein the light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 261 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 268.

[00202] Also disclosed are isolated polynucleotides that encode an antibody or antigen- binding fragment comprising a light chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 282. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a heavy chain variable region, wherein the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 284. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment comprising a light chain variable region and a heavy chain variable region, wherein the light chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 282 and the heavy chain variable region amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 284.

[00203] Also disclosed are isolated polynucleotides that encode an antibody comprising a light chain, wherein the light chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 283. In some embodiments, the isolated polynucleotides encode an antibody comprising a heavy chain, wherein the heavy chain amino acid sequence is substantially the same as, or identical to, SEQ ID NO: 285. In some embodiments, the isolated polynucleotides encode an antibody comprising a light chain and a heavy chain, wherein the light chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 283 and a heavy chain amino acid sequence substantially the same as, or identical to, SEQ ID NO: 285.

[00204] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 1, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 2, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 3, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 8, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 9, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 10, wherein the CDRs are defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 1, wherein the CDR is defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 2, wherein the CDR is defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 3, wherein the CDR is defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 8, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 9, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 10, wherein the CDR is defined according to the IMGT method.

[00205] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 4, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 5, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 3, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 11, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 12, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 13, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 4, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 5, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 3, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 11, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 12, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 13, wherein the CDR is defined according to the KABAT method.

[00206] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 55, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 56, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 57, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 62, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 63, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 64, wherein the CDRs are defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 55, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 56, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 57, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 62, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 63, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 64, wherein the CDR is defined according to the IMGT method.

[00207] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 58, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 59, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 57, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 65, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 66, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 64, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 58, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 59, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 57, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 65, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 66, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 64, wherein the CDR is defined according to the KABAT method.

[00208] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 84, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 85, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 86, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 90, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 91, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 92, wherein the CDRs are defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 84, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 85, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 86, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 90, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 91, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 92, wherein the CDR is defined according to the IMGT method.

[00209] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 87, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 32, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 86, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 93, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 94, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 95, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 87, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 32, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 86, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 93, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 94, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 95, wherein the CDR is defined according to the KABAT method.

[00210] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 112, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 2, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 113, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 118, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 119, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 120, wherein the CDRs are defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 112, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 2, wherein the CDR is defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 113, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 118, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 119, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 120, wherein the CDR is defined according to the IMGT method.

[00211] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 114, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 115, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 113, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 121, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 122, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 123, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 114, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 115, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 113, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 121, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 122, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 123, wherein the CDR is defined according to the KABAT method.

[00212] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 55, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 140, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 141, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 145, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 146, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 147, wherein the CDRs are defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 55, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 140, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 141, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 145, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 146, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 147, wherein the CDR is defined according to the IMGT method.

[00213] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 58, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 142, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 141, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 148, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 149, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 150, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 58, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 142, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 141, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 148, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 149, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 150, wherein the CDR is defined according to the KABAT method.

[00214] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 55, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 56, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 57, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 168, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 169, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 170, wherein the CDRs are defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 55, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 56, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 57, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 168, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 169, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 170, wherein the CDR is defined according to the IMGT method.

[00215] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 58, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 59, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 57, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 171, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 172, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 173, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 58, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 59, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 57, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 171, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 172, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 173, wherein the CDR is defined according to the KABAT method.

[00216] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 187, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 188, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 189, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 194, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 195, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 196, wherein the CDRs are defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 187, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 188, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 189, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 194, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 195, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 196, wherein the CDR is defined according to the IMGT method.

[00217] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 190, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 191, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 189, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 197, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 198, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 199, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 190, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 191, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 189, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 197, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 198, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 199, wherein the CDR is defined according to the KABAT method.

[00218] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 217, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 188, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 189, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 194, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 221, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 196, wherein the CDRs are defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 217, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 188, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 189, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 194, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 221, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 196, wherein the CDR is defined according to the IMGT method.

[00219] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 218, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 191, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 189, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 197, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 222, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 199, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 218, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 191, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 189, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 197, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 222, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 199, wherein the CDR is defined according to the KABAT method.

[00220] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 233, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 234, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 235, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 194, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 195, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 240, wherein the CDRs are defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 233, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 234, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 235, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 194, wherein the CDR is defined according to the IMGT method. In some

- I l l - embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 195, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 240, wherein the CDR is defined according to the IMGT method.

[00221] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 236, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 237, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 235, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 241, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 198, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 242, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 236, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 237, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 235, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 241, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 198, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 242, wherein the CDR is defined according to the KABAT method.

[00222] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 257, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 188, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 258, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 8, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 262, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 263, wherein the CDRs are defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 257, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 188, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 258, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 8, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 262, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 263, wherein the CDR is defined according to the IMGT method.

[00223] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 259, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 191, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 258, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 264, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 265, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 266, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 259, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 191, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 258, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 264, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 265, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 266, wherein the CDR is defined according to the KABAT method.

[00224] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 1, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 2, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 3, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 8, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 9, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 10, wherein the CDRs are defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 1, wherein the CDR is defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 2, wherein the CDR is defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 3, wherein the CDR is defined according to the IMGT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 8, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 9, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 10, wherein the CDR is defined according to the IMGT method.

[00225] Described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 4, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 115, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 3, a heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 11, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 12, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 13, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 4, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 115, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 3, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 11, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 12, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 13, wherein the CDR is defined according to the KABAT method.

[00226] Described herein are isolated polynucleotide nucleotide sequences substantially similar to, or the same as, SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 23, SEQ ID NO: 24, and SEQ ID NO 25. In other embodiments, the isolated polynucleotides are substantially similar to, or the same as, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 18, SEQ ID NO: 26, SEQ ID NO: 27, and SEQ ID NO 28.

[00227] Described herein are isolated polynucleotide nucleotide sequences substantially similar to, or the same as, SEQ ID NO: 69, SEQ ID NO: 70, SEQ ID NO: 71, SEQ ID NO: 76, SEQ ID NO: 77, and SEQ ID NO 78. In other embodiments, the isolated polynucleotides are substantially similar to, or the same as, SEQ ID NO: 72, SEQ ID NO: 73, SEQ ID NO: 71, SEQ ID NO: 79, SEQ ID NO: 80, and SEQ ID NO 81.

[00228] Described herein are isolated polynucleotide nucleotide sequences substantially similar to, or the same as, SEQ ID NO: 98, SEQ ID NO: 99, SEQ ID NO: 100, SEQ ID NO: 104, SEQ ID NO: 105, and SEQ ID NO 106. In other embodiments, the isolated polynucleotides are substantially similar to, or the same as, SEQ ID NO: 101, SEQ ID NO: 40, SEQ ID NO: 100, SEQ ID NO: 107, SEQ ID NO: 108, and SEQ ID NO 109.

[00229] Described herein are isolated polynucleotide nucleotide sequences substantially similar to, or the same as, SEQ ID NO: 126, SEQ ID NO: 17, SEQ ID NO: 127, SEQ ID NO:

132, SEQ ID NO: 133, and SEQ ID NO 134. In other embodiments, the isolated polynucleotides are substantially similar to, or the same as, SEQ ID NO: 128, SEQ ID NO: 129, SEQ ID NO: 127, SEQ ID NO: 135, SEQ ID NO: 136, and SEQ ID NO 137.

[00230] Described herein are isolated polynucleotide nucleotide sequences substantially similar to, or the same as, SEQ ID NO: 69, SEQ ID NO: 153, SEQ ID NO: 154, SEQ ID NO: 158, SEQ ID NO: 159, and SEQ ID NO 160. In other embodiments, the isolated polynucleotides are substantially similar to, or the same as, SEQ ID NO: 72, SEQ ID NO: 155, SEQ ID NO: 154, SEQ ID NO: 161, SEQ ID NO: 162, and SEQ ID NO 163.

[00231] Described herein are isolated polynucleotide nucleotide sequences substantially similar to, or the same as, SEQ ID NO: 69, SEQ ID NO: 70, SEQ ID NO: 71, SEQ ID NO: 179, SEQ ID NO: 180, and SEQ ID NO 181. In other embodiments, the isolated polynucleotides are substantially similar to, or the same as, SEQ ID NO: 72, SEQ ID NO: 73, SEQ ID NO: 176, SEQ ID NO: 182, SEQ ID NO: 183, and SEQ ID NO 184.

[00232] Described herein are isolated polynucleotide nucleotide sequences substantially similar to, or the same as, SEQ ID NO: 202, SEQ ID NO: 203, SEQ ID NO: 204, SEQ ID NO: 209, SEQ ID NO: 210, and SEQ ID NO 211. In other embodiments, the isolated polynucleotides are substantially similar to, or the same as, SEQ ID NO: 205, SEQ ID NO: 206, SEQ ID NO: 204, SEQ ID NO: 212, SEQ ID NO: 213, and SEQ ID NO 214.

[00233] Described herein are isolated polynucleotide nucleotide sequences substantially similar to, or the same as, SEQ ID NO: 225, SEQ ID NO: 203, SEQ ID NO: 204, SEQ ID NO: 209, SEQ ID NO: 229, and SEQ ID NO 211. In other embodiments, the isolated polynucleotides are substantially similar to, or the same as, SEQ ID NO: 226, SEQ ID NO: 206, SEQ ID NO: 204, SEQ ID NO: 212, SEQ ID NO: 230, and SEQ ID NO 214.

[00234] Described herein are isolated polynucleotide nucleotide sequences substantially similar to, or the same as, SEQ ID NO: 245, SEQ ID NO: 246, SEQ ID NO: 247, SEQ ID NO: 209, SEQ ID NO: 210, and SEQ ID NO 252. In other embodiments, the isolated polynucleotides are substantially similar to, or the same as, SEQ ID NO: 248, SEQ ID NO: 249, SEQ ID NO: 247, SEQ ID NO: 253, SEQ ID NO: 213, and SEQ ID NO 254.

[00235] Described herein are isolated polynucleotide nucleotide sequences substantially similar to, or the same as, SEQ ID NO: 269, SEQ ID NO: 203, SEQ ID NO: 270, SEQ ID NO: 274, SEQ ID NO: 275, and SEQ ID NO 276. In other embodiments, the isolated polynucleotides are substantially similar to, or the same as, SEQ ID NO: 271, SEQ ID NO: 206, SEQ ID NO: 270, SEQ ID NO: 277, SEQ ID NO: 278, and SEQ ID NO 279.

[00236] Described herein are isolated polynucleotide nucleotide sequences substantially similar to, or the same as, SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 288, SEQ ID NO: 24, and SEQ ID NO 25. In other embodiments, the isolated polynucleotides are substantially similar to, or the same as, SEQ ID NO: 19, SEQ ID NO: 129, SEQ ID NO: 18, SEQ ID NO: 289, SEQ ID NO: 290, and SEQ ID NO 28.

[00237] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein the light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 1, the light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 2, and the light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence SEQ ID NO: 3, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 1, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 2, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated

polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 3, wherein the CDR is defined according to the IMGT method.

[00238] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein the light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 4, the light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 5, and the light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence SEQ ID NO: 3, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 4, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 5, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 3, wherein the CDR is defined according to the KABAT method.

[00239] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein the heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 8, the heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 9, and the heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 8, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 9, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 10, wherein the CDR is defined according to the IMGT method.

[00240] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein the heavy chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of

SEQ ID NO: 11, the heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 12, and the heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence SEQ ID

NO: 13, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID

NO: 11, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID

NO: 12, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID

NO: 13, wherein the CDR is defined according to the KABAT method. [00241] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 55, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 56, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 57, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 55, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated

polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 56, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated

polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 57, wherein the CDR is defined according to the IMGT method.

[00242] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 58, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 59, a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 57, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 58, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 59, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 57, wherein the CDR is defined according to the KABAT method.

[00243] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 62, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 63, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 64, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 62, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 63, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 64, wherein the CDR is defined according to the IMGT method.

[00244] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 65, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 66, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 64, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 65, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 66, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 64, wherein the CDR is defined according to the KABAT method.

[00245] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 84, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 85, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 86, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 84, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated

polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 85, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated

polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 86, wherein the CDR is defined according to the IMGT method.

[00246] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 87, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 32, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 86, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 87, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 32, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 86, wherein the CDR is defined according to the KABAT method.

[00247] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 90, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 91, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 92, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 90, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 91, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 92, wherein the CDR is defined according to the IMGT method.

[00248] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 93, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 94, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 95, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 93, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO:

94, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO:

95, wherein the CDR is defined according to the KABAT method.

[00249] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 112, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 2, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 113, In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 112, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 2, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 113, wherein the CDR is defined according to the IMGT method.

[00250] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 114, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 115, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 113, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 114, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 115, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 113, wherein the CDR is defined according to the KABAT method.

[00251] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 118, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 119, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID

NO: 120, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID

NO: 118, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO:

119, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO:

120, wherein the CDR is defined according to the IMGT method.

[00252] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 121, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 122, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 123, wherein the CDRs are defined according to the KABAT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 121, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 122, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 123, wherein the CDR is defined according to the KABAT method.

[00253] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 55, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 140, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 141, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 55, wherein the

CDR is defined according to the IMGT method. In some embodiments, the isolated

polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 140, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 141, wherein the CDR is defined according to the IMGT method.

[00254] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 58, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 142, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 141, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 58, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 142, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 141, wherein the CDR is defined according to the KABAT method.

[00255] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 145, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 146, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 147, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 145, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 146, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 147, wherein the CDR is defined according to the IMGT method.

[00256] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 148, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 149, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 150, wherein the CDRs are defined according to the KABAT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 148, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 149, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 150, wherein the CDR is defined according to the KABAT method.

[00257] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 55, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 56, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 57, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 55, wherein the

CDR is defined according to the IMGT method. In some embodiments, the isolated

polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 56, wherein the

CDR is defined according to the IMGT method. In some embodiments, the isolated

polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 57, wherein the

CDR is defined according to the IMGT method. [00258] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 58, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 59, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 57, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 58, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 59, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 57, wherein the CDR is defined according to the KABAT method.

[00259] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 168, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 169, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 170, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 168, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO:

169, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO:

170, wherein the CDR is defined according to the IMGT method.

[00260] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 171, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 172, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 173, wherein the CDRs are defined according to the KABAT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 171, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 172, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 173, wherein the CDR is defined according to the KABAT method.

[00261] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 187, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 188, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 189, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 187, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 188, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 189, wherein the CDR is defined according to the IMGT method.

[00262] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 190, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 191, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 189, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 190, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 191, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 189, wherein the CDR is defined according to the KABAT method.

[00263] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 194, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 195, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 196, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 194, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO:

195, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO:

196, wherein the CDR is defined according to the IMGT method.

[00264] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 197, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 198, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 199, wherein the CDRs are defined according to the KABAT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 197, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 198, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 199, wherein the CDR is defined according to the KABAT method.

[00265] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 217, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 188, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 189, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 217, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 188, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 189, wherein the CDR is defined according to the IMGT method.

[00266] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 218, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 191, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 189, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 218, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 191, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 189, wherein the CDR is defined according to the KABAT method.

[00267] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 194, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 221, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 196, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 194, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 221, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 196, wherein the CDR is defined according to the IMGT method.

[00268] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 197, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 222, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID

NO: 199, wherein the CDRs are defined according to the KABAT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 197, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 222, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 199, wherein the CDR is defined according to the KABAT method.

[00269] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 233, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 234, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 235, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 233, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 24, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated

polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 235, wherein the CDR is defined according to the IMGT method.

[00270] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 236, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 237, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 235, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 236, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 237, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 235, wherein the CDR is defined according to the KABAT method.

[00271] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 194, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 195, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 240, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 194, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 195, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 240, wherein the CDR is defined according to the IMGT method.

[00272] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 241, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 198, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID

NO: 242, wherein the CDRs are defined according to the KABAT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 241, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 198, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 242, wherein the CDR is defined according to the KABAT method.

[00273] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 257, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 188, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 258, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 257, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 188, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 258, wherein the CDR is defined according to the IMGT method.

[00274] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDR1 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 259, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 191, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 258, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR1 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 259, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 191, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 258, wherein the CDR is defined according to the KABAT method. [00275] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 8, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 262, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 263, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 8, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO:

262, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO:

263, wherein the CDR is defined according to the IMGT method.

[00276] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 264, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 265, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 266, wherein the CDRs are defined according to the KABAT method. In some

embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 264, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 265, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 266, wherein the CDR is defined according to the KABAT method.

[00277] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 1, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 2, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 3, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 1, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated

polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 2, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated

polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 3, wherein the CDR is defined according to the IMGT method.

[00278] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a light chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 4, a light chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 115, and a light chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 3, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 4, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 115, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a light chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 3, wherein the CDR is defined according to the KABAT method.

[00279] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ

ID NO: 8, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 9, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 8, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 9, wherein the CDR is defined according to the IMGT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 10, wherein the CDR is defined according to the IMGT method.

[00280] Also described herein are isolated polynucleotides that encode an antibody or antigen-binding fragment specific for folate receptor alpha (FRa) wherein a heavy chain CDRl of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 11, a heavy chain CDR2 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 12, and a heavy chain CDR3 of the encoded antibody is substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDRl substantially the same as, or identical to, the amino acid sequence of SEQ ID NO: 11, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR2 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO:

12, wherein the CDR is defined according to the KABAT method. In some embodiments, the isolated polynucleotides encode an antibody or antigen-binding fragment that includes a heavy chain CDR3 substantially the same as, or identical to, the amino acid sequence of SEQ ID NO:

13, wherein the CDR is defined according to the KABAT method.

[00281] Polynucleotides encoding engineered antigen-binding proteins also are within the scope of the disclosure. In some embodiments, the polynucleotides described (and the peptides they encode) include a leader sequence. Any leader sequence known in the art may be employed. The leader sequence may include, but is not limited to, a restriction site or a translation start site. [00282] The antibodies or antigen-binding fragments described herein include variants having single or multiple amino acid substitutions, deletions, or additions that retain the biological properties (e.g., binding affinity or immune effector activity) of the described antibodies or antigen-binding fragments. The skilled person may produce variants having single or multiple amino acid substitutions, deletions, or additions. These variants may include: (a) variants in which one or more amino acid residues are substituted with conservative or nonconservative amino acids, (b) variants in which one or more amino acids are added to or deleted from the polypeptide, (c) variants in which one or more amino acids include a substituent group, and (d) variants in which the polypeptide is fused with another peptide or polypeptide such as a fusion partner, a protein tag or other chemical moiety, that may confer useful properties to the polypeptide, such as, for example, an epitope for an antibody, a polyhistidine sequence, a biotin moiety and the like. Antibodies or antigen-binding fragments described herein may include variants in which amino acid residues from one species are substituted for the corresponding residue in another species, either at the conserved or nonconserved positions. In other embodiments, amino acid residues at nonconserved positions are substituted with conservative or nonconservative residues. The techniques for obtaining these variants, including genetic (suppressions, deletions, mutations, etc.), chemical, and enzymatic techniques, are known to the person having ordinary skill in the art.

[00283] The antibodies or antigen-binding fragments described herein may embody several antibody isotypes, such as IgM, IgD, IgG, IgA and IgE. Antibody or antigen-binding fragment thereof specificity is largely determined by the amino acid sequence, and arrangement, of the CDRs. Therefore, the CDRs of one isotype may be transferred to another isotype without altering antigen specificity. Alternatively, techniques have been established to cause hybridomas to switch from producing one antibody isotype to another (isotype switching) without altering antigen specificity. Accordingly, such antibody isotypes are within the scope of the described antibodies or antigen-binding fragments

[00284] In some embodiments the isolated polynucleotides capable of encoding the domains provided herein may be included on the same, or different, vectors to produce an antibody or antigen-binding fragment. The vectors can be expression vectors. Recombinant expression vectors containing a sequence encoding a polypeptide of interest are thus

contemplated as within the scope of this disclosure. The expression vector may contain one or more additional sequences such as but not limited to regulatory sequences (e.g., promoter, enhancer), a selection marker, and a polyadenylation signal. Vectors for transforming a wide variety of host cells are well known and include, but are not limited to, plasmids, phagemids, cosmids, baculoviruses, bacmids, bacterial artificial chromosomes (BACs), yeast artificial chromosomes (YACs), as well as other bacterial, yeast and viral vectors.

[00285] Recombinant expression vectors within the scope of the description include synthetic, genomic, or cDNA-derived nucleic acid fragments that encode at least one recombinant protein which may be operably linked to suitable regulatory elements. Such regulatory elements may include a transcriptional promoter, sequences encoding suitable mRNA ribosomal binding sites, and sequences that control the termination of transcription and translation. Expression vectors, especially mammalian expression vectors, may also include one or more nontranscribed elements such as an origin of replication, a suitable promoter and enhancer linked to the gene to be expressed, other 5' or 3' flanking nontranscribed sequences, 5' or 3' nontranslated sequences (such as necessary ribosome binding sites), a polyadenylation site, splice donor and acceptor sites, or transcriptional termination sequences. An origin of replication that confers the ability to replicate in a host may also be incorporated.

[00286] The transcriptional and translational control sequences in expression vectors to be used in transforming vertebrate cells may be provided by viral sources. Exemplary vectors may be constructed as described by Okayama and Berg, 3 Mol. Cell. Biol. 280 (1983).

[00287] In some embodiments, the antibody- or antigen-binding fragment-encoding sequence is placed under control of a powerful constitutive promoter, such as the promoters for the following genes: hypoxanthine phosphoribosyl transferase (HPRT), adenosine deaminase, pyruvate kinase, beta-actin, human myosin, human hemoglobin, human muscle creatine, and others. In addition, many viral promoters function constitutively in eukaryotic cells and are suitable for use with the described embodiments. Such viral promoters include without limitation, Cytomegalovirus (CMV) immediate early promoter, the early and late promoters of SV40, the Mouse Mammary Tumor Virus (MMTV) promoter, the long terminal repeats (LTRs) of Maloney leukemia virus, Human Immunodeficiency Virus (HIV), Epstein Barr Virus (EBV), Rous Sarcoma Virus (RSV), and other retroviruses, and the thymidine kinase promoter of Herpes Simplex Virus. In one embodiment, the antibody or antigen-binding fragment thereof coding sequence is placed under control of an inducible promoter such as the metallothionein promoter, tetracycline-inducible promoter, doxycycline-inducible promoter, promoters that contain one or more interferon-stimulated response elements (ISRE) such as protein kinase R 2',5'- oligoadenylate synthetases, Mx genes, ADAR1, and the like.

[00288] Vectors described herein may contain one or more Internal Ribosome Entry

Site(s) (IRES). Inclusion of an IRES sequence into fusion vectors may be beneficial for enhancing expression of some proteins. In some embodiments the vector system will include one or more polyadenylation sites (e.g., SV40), which may be upstream or downstream of any of the aforementioned nucleic acid sequences. Vector components may be contiguously linked, or arranged in a manner that provides optimal spacing for expressing the gene products (i.e., by the introduction of "spacer" nucleotides between the ORFs), or positioned in another way. Regulatory elements, such as the IRES motif, may also be arranged to provide optimal spacing for expression.

[00289] The vectors may comprise selection markers, which are well known in the art. Selection markers include positive and negative selection markers, for example, antibiotic resistance genes (e.g., neomycin resistance gene, a hygromycin resistance gene, a kanamycin resistance gene, a tetracycline resistance gene, a penicillin resistance gene), glutamate sythase genes, HSV-TK, HSV-TK derivatives for ganciclovir selection, or bacterial purine nucleoside phosphorylase gene for 6-methylpurine selection (Gadi et al, 7 Gene Ther. 1738-1743 (2000)). A nucleic acid sequence encoding a selection marker or the cloning site may be upstream or downstream of a nucleic acid sequence encoding a polypeptide of interest or cloning site.

[00290] The vectors described herein may be used to transform various cells with the genes encoding the described antibodies or antigen-binding fragments. For example, the vectors may be used to generate antibody or antigen-binding fragment-producing cells. Thus, another aspect features host cells transformed with vectors comprising a nucleic acid sequence encoding an antibody or antigen-binding fragment thereof that specifically binds FRa, such as the antibodies or antigen-binding fragments described and exemplified herein.

[00291] Numerous techniques are known in the art for the introduction of foreign genes into cells and may be used to construct the recombinant cells for purposes of carrying out the described methods, in accordance with the various embodiments described and exemplified herein. The technique used should provide for the stable transfer of the heterologous gene sequence to the host cell, such that the heterologous gene sequence is heritable and expressible by the cell progeny, and so that the necessary development and physiological functions of the recipient cells are not disrupted. Techniques which may be used include but are not limited to chromosome transfer (e.g., cell fusion, chromosome mediated gene transfer, micro cell mediated gene transfer), physical methods (e.g., transfection, spheroplast fusion, microinjection, electroporation, liposome carrier), viral vector transfer (e.g., recombinant DNA viruses, recombinant RNA viruses) and the like (described in Cline, 29 Pharmac. Ther. 69-92 (1985)). Calcium phosphate precipitation and polyethylene glycol (PEG)-induced fusion of bacterial protoplasts with mammalian cells may also be used to transform cells. [00292] Also provided are cells capable of expressing the described vectors. The cells may be eukaryotic cells, yeast cells, plant cells or bacteria. Cells suitable for use in the expression of the antibodies or antigen-binding fragments described herein are preferably eukaryotic cells, more preferably cells of plant, rodent, or human origin, for example but not limited to NSO, CHO, CHOK1, perC.6, Tk-tsl3, BHK, HEK293 cells, COS-7, T98G, CV- 1/EBNA, L cells, C127, 3T3, HeLa, NS 1, Sp2/0 myeloma cells, and BHK cell lines, among others. In addition, expression of antibodies may be accomplished using hybridoma cells. In preferred embodiments, the eukaryotic cell is a CHO cell. Methods for producing hybridomas are well established in the art.

[00293] Cells transformed with expression vectors described herein may be selected or screened for recombinant expression of the antibodies or antigen-binding fragments described herein. Recombinant-positive cells are expanded and screened for subclones exhibiting a desired phenotype, such as high level expression, enhanced growth properties, or the ability to yield proteins with desired biochemical characteristics, for example, due to protein modification or altered post-translational modifications. These phenotypes may be due to inherent properties of a given subclone or to mutation. Mutations may be effected through the use of chemicals, UV- wavelength light, radiation, viruses, insertional mutagens, inhibition of DNA mismatch repair, or a combination of such methods.

Methods for detecting FRa in a biological sample

[00294] Provided herein are methods for detecting folate receptor alpha (FRa) in a biological sample. In some embodiments, the method involves exposing the sample to any one of the antibodies or antigen-binding fragments described herein and detecting FRa. In some embodiments, the biological sample is derived from urine, blood, serum, plasma, saliva, ascites, circulating cells, circulating tumor cells, cells that are not tissue associated, tissues, surgically resected tumor tissue, biopsies, fine needle aspiration samples, or histological preparations. In some embodiments, the biological sample is derived from a human or nonhuman primate. In some embodiments, the antibody is labeled. In some embodiments, the label is a radiolabel, an epitope tag, biotin, a chromophore label, a fluorophore label, an electrochemiluminescence (ECL) label, or an enzyme. In preferred embodiments, the electrochemiluminescence (ECL) label is a sulfo-tag. In some embodiments, the method further involves exposing the sample to a second antibody or antigen-binding fragment of any one of the described antibodies. In some embodiments, the second antibody or antigen-binding fragment is immobilized to a solid support.

In preferred embodiments, the second antibody or antigen-binding fragment is biotinylated and the solid support is coated with streptavidin, and the isolated antibody or antigen-binding fragment is immobilized to the solid support by the binding of biotin to streptavidin. In some embodiments, the presence of folate receptor alpha (FRa) in the sample is detected using westem blot, immunohistochemistry, immunofluorescence, flow cytometry, radioimmunoassay, immunoprecipitation, electrochemiluminescence immunoassay (ECLIA), or ELISA. In some embodiments, the sample is diluted prior to detecting folate receptor alpha (FRa) in the sample. In some embodiments, the sample is centrifuged, vortexed, or both, prior to detecting folate receptor alpha (FRa) in the sample. In some embodiments, the level of folate receptor alpha (FRa) in the sample is quantified. In some embodiments, the sample is exposed to MORAb-003 prior to detecting folate receptor alpha (FRa) in the sample.

[00295] Various combinations of the antibodies, or antigen-binding fragments thereof, may be used to detect FRa in a sample, as depicted in Table 2.

Table 2: Antibody combinations for detecting FRa in a sample

[00296] In some embodiments, the method involves exposing the sample to a first isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method, or a first isolated antibody or antigen- binding fragment comprising a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 5, 2016 that has been assigned Accession No. PTA-123090 and a second isolated antibody or antigen-binding fragment with a light chain CDRl comprising the amino acid sequence of SEQ ID NO: 31, a light chain CDR2 comprising the amino acid sequence of SEQ ID NO: 32, a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 33, a heavy chain CDRl comprising the amino acid sequence of SEQ ID NO: 35, a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 36, and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 37 or the isolated antibody that is produced by antibody- producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 19, 2011 that has been assigned Accession No. PTA-11884, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00297] In other embodiments, the method involves exposing the sample to a first isolated antibody or antigen-binding fragment with a light chain CDRl comprising the amino acid sequence of SEQ ID NO: 31, a light chain CDR2 comprising the amino acid sequence of SEQ ID NO: 32, a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 33, a heavy chain CDRl comprising the amino acid sequence of SEQ ID NO: 35, a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 36, and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 37 or the isolated antibody that is produced by antibody- producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 19, 2011 that has been assigned Accession No. PTA-11884 and a second isolated antibody or antigen-binding fragment comprising a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method, or a second isolated antibody or antigen-binding fragment comprising a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method, or the second isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 5, 2016 that has been assigned Accession No. PTA- 123090, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00298] In other embodiments, the first isolated antibody or antigen-binding fragment or the second isolated antibody or antigen-binding fragment comprises a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method, or a isolated antibody or antigen- binding fragment comprising a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 5, 2016 that has been assigned Accession No. PTA-123090.

[00299] In other embodiments, the first isolated antibody or antigen-binding fragment or the second isolated antibody or antigen-binding fragment comprises the amino acid sequence of SEQ ID NO: 31, a light chain CDR2 comprising the amino acid sequence of SEQ ID NO: 32, a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 33, a heavy chain CDR1 comprising the amino acid sequence of SEQ ID NO: 35, a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 36, and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 37 or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 19, 2011 that has been assigned Accession No. PTA-11884.

[00300] In other embodiments, the first isolated antibody or antigen-binding fragment or the second isolated antibody or antigen-binding fragment comprises a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method, or a isolated antibody or antigen- binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123097.

[00301] In other embodiments, the first isolated antibody or antigen-binding fragment or the second isolated antibody or antigen-binding fragment comprises a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 55, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 56, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 62, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 63, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 64, wherein the CDRs are defined according to the IMGT method, or an isolated antibody or antigen-binding fragment comprising a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 58, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 59, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 65, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 66, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 64, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123091, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00302] In other embodiments, the first isolated antibody or antigen-binding fragment or the second isolated antibody or antigen-binding fragment comprises a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 84, a light chain CDR2 amino acid sequence substantially the same as, or identical to SEQ ID NO: 85, a light chain

CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 86, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 90, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO:

91, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ

ID NO: 92, wherein the CDRs are defined according to the IMGT method, or a isolated antibody or antigen-binding fragment comprising a light chain an isolated antibody or antigen-binding fragment comprising a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 87, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 32, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 86, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 93, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 94, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 95, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123098, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00303] In other embodiments, the first isolated antibody or antigen-binding fragment or the second isolated antibody or antigen-binding fragment comprises an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 112, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 113, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 118, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 119, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 120, wherein the CDRs are defined according to the IMGT method, or a isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 114, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 115, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 113, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 121, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 122, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 123, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123093, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled. [00304] In other embodiments, the first isolated antibody or antigen-binding fragment or the second isolated antibody or antigen-binding fragment comprises an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 55, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 140, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 141, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 145, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 146, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 147, wherein the CDRs are defined according to the IMGT method, or an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 58, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 142, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 141, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 148, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 149, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 150, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123094, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00305] In other embodiments, the first isolated antibody or antigen-binding fragment or the second isolated antibody or antigen-binding fragment comprises an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 55, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 56, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 168, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 169, and a heavy chain

CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 170, wherein the CDRs are defined according to the IMGT method, or an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acide sequence substantially the same as, or identical to, SEQ ID NO: 58, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 59, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 171, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 172, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 173, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123092, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00306] In other embodiments, the first isolated antibody or antigen-binding fragment or the second isolated antibody or antigen-binding fragment comprises an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 187, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 188, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 194, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 195, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 196, wherein the CDRs are defined according to the IMGT method, or a second isolated antibody or antigen- binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to SEQ ID NO: 190, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 191, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 197, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 198, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 199, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody- producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123098, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00307] In other embodiments, the first isolated antibody or antigen-binding fragment or the second isolated antibody or antigen-binding fragment comprises an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 217, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 188, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 194, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 221, and a heavy chain

CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 196, wherein the CDRs are defined according to the IMGT method, or an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 218, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 191, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 197, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 222, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 199, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas,

Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123095, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00308] In other embodiments, the first isolated antibody or antigen-binding fragment or the second isolated antibody or antigen-binding fragment comprises an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 233, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 234, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 235, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 194, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 195, and a heavy chain

CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 240, wherein the CDRs are defined according to the IMGT method, or a isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 236, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 237, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 235, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 241, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 198, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 242, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123101, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00309] In other embodiments, the first isolated antibody or antigen-binding fragment or the second isolated antibody or antigen-binding fragment comprises an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 257, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 188, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 258, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 262, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 263, wherein the CDRs are defined according to the IMGT method, or an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 259, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 191, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 258, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 264, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 265, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 266, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123096, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00310] In other embodiments, the first isolated antibody or antigen-binding fragment or the second isolated antibody or antigen-binding fragment comprises an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method, or an isolated antibody or antigen-binding fragment comprising SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 115, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123100, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00311] Various combinations of the antibodies, or antigen-binding fragments thereof, may be used to detect FRa in a sample. For example, any first isolated antibody or antibody fragment in paragraphs [00297] through [00309] may be paired with any second isolated antibody or antibody fragment in paragraphs [00297] through [00309]. In preferred embodiments, the first isolated antibody or antigen-binding fragment and the second isolated antibody or antigen-binding fragment are different.

[00312] In some embodiments, the biological sample is derived from urine, blood, serum, plasma, saliva, ascites, circulating cells, circulating tumor cells, cells that are not tissue associated, tissues, surgically resected tumor tissue, biopsies, fine needle aspiration samples, or histological preparations. In some embodiments, the biological sample is derived from a human or nonhuman primate. In some embodiments, the antibody is labeled. The described antibodies and antigen-binding fragments may be detectably labeled. In some embodiments labeled antibodies and antigen-binding fragments may facilitate the detection FRa via the methods described herein. Many such labels are readily known to those skilled in the art. For example, suitable labels include, but should not be considered limited to, radiolabels, fluorescent labels

(such as DyLight® 649), epitope tags, biotin, chromophore labels, ECL labels, or enzymes. More specifically, the described labels include ruthenium, ^m In-DOTA, ^m In- diethylenetriaminepentaacetic acid (DTP A), horseradish peroxidase, alkaline phosphatase and beta-galactosidase, poly-histidine (HIS tag), acridine dyes, cyanine dyes, fluorone dyes, oxazin dyes, phenanthridine dyes, rhodamine dyes, Alexafluor® dyes, and the like. In some

embodiments, the label is a radiolabel, an epitope tag, biotin, a chromophore label, a fluorophore label, an electrochemiluminescence (ECL) label, or an enzyme. In preferred embodiments, the electrochemiluminescence (ECL) label is a sulfo-tag.

[00313] In some embodiments, the first isolated antibody or antigen-binding fragment is biotinylated and the solid support is coated with streptavidin, and the isolated antibody or antigen- binding fragment is immobilized to the solid support by the binding of biotin to streptavidin. In some embodiments, the presence of folate receptor alpha (FRa) in the sample is detected using western blot, immunohistochemistry, immunofluorescence, flow cytometry, radioimmunoassay, immunoprecipitation, electrochemiluminescence immunoassay (ECLIA), or ELISA. In some embodiments, the level of FRa in the sample is quantified.

[00314] In some embodiments described herein detection of FRa-expressing cancer cells in a subject may be used to determine that the subject may be treated with a therapeutic agent directed against FRa. In some embodiments the therapeutic agent directed against FRa may be an antibody, such as farletuzumab (MORAb-003). In some embodiments, the sample is exposed to MORAb-003 prior to detecting FRa in the sample.

Methods for Diagnosing, Monitoring and Treating Folate Receptor Alpha (FRa)- Expressing Cancer

[00315] Provided herein are methods for diagnosing a folate receptor alpha (FRa)- expressing cancer in a subject. FRa-expressing cancers include ovarian, breast, thyroid, colorectal, endometrial, fallopian tube, or lung cancer of epithelial origin in a subject. In some embodiments, as described above, detecting FRa in a sample, such as a histological sample, a fine needle aspirate sample, resected tumor tissue, circulating cells, circulating tumor cells, and the like, provides the ability to diagnose cancer in the subject from whom the sample was obtained. In some embodiments, it may already be known that the subject from whom the sample was obtained has cancer, but the type of cancer afflicting the subject may not yet have been diagnosed or a preliminary diagnosis may be unclear, thus detecting FRa in a sample obtained from the subject can allow for, or clarify, diagnosis of the cancer.

[00316] In some embodiments, the described methods involve exposing the biological sample of the subject to any one of the antibodies or antigen-binding fragments described herein.

In some embodiments, the described methods involve exposing the biological sample of the subject to an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by any one of the antibodies or antigen binding fragments described herein. In some embodiments, the described methods involve quantifying the amount of FRa present in the sample that is bound by the antibody or antigen-binding fragment. In some embodiments, the described methods involve comparing the amount of FRa present in the sample to a known standard. In some embodiments, the described methods involve determining whether the subject's FRa levels fall within the levels of FRa associated with cancer.

[00317] Also described herein are methods for monitoring a folate receptor alpha (FRa)- expressing cancer in a subject. In some embodiments, the described methods involve exposing the biological sample of the subject to any one of the antibodies or antigen-binding fragments described herein. In some embodiments, the described methods involve exposing the biological sample of the subject to an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by the antibody or antigen binding fragment of any one of the antibodies or antigen-binding fragments described herein. In some embodiments, the described methods involve quantifying the amount of FRa present in the sample that is bound by the antibody or antigen-binding fragment. In some embodiments, the described methods involve comparing the amount of FRa present in the sample to a known standard. In some embodiments, the described methods involve comparing the amount of FRa present in the sample to a biological sample obtained from the subject at an earlier point in time. In some embodiments, the described methods involve determining whether the subject's FRa levels are indicative of cancer progression, regression or stable disease.

[00318] Also provided herein are methods for treating a folate receptor alpha (FRa)- expressing cancer in a subject. In some embodiments, the described methods involve exposing the biological sample of the subject to any one of the antibodies or antigen-binding fragments described herein. In some embodiments, the described methods involve exposing the biological sample of the subject to an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by the antibody or antigen binding fragment of any one of the antibodies or antigen-binding fragments described herein. In some embodiments, the described methods involve quantifying the amount of FRa present in the sample that is bound by the antibody or antigen-binding fragment. In some embodiments, the described methods involve comparing the amount of FRa present in the sample to a known standard. In some embodiments, the described methods involve determining whether the subject's FRa levels fall within the levels of FRa associated with cancer. In some embodiments, the described methods involve administering to the subject, or prescribing, a treatment for the cancer. [00319] In some embodiments of the described methods, the antibody or antigen- binding fragment of any one of the antibodies or antigen-binding fragments described herein is labeled. In some embodiments, the label is a radiolabel, an epitope tag, biotin, a chromophore label, a fluorophore label, an electrochemiluminescence (ECL) label, or an enzyme. In preferred embodiments, the electrochemiluminescence (ECL) label is a sulfo-tag.

[00320] In some embodiments of the methods described herein, the step of exposing a biological sample of the subject to the antibody or antigen-binding fragment of any one of the antibodies or antigen-binding fragments described herein or an antibody or antigen-binding fragment capable of binding the epitope of folate receptor alpha (FRa) that is bound by the antibody or antigen binding fragment of any one of the antibodies or antigen-binding fragments described herein further comprises exposing the biological sample of the subject to a second antibody or antigen-binding fragment capable of binding FRa.

[00321] In some embodiments of the methods described herein, the antibody or antigen- binding fragment or the second antibody or antigen-binding fragment is the isolated antibody or antigen-binding fragment which includes a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method. In some embodiments of the methods described herein, the antibody or antigen-binding fragment is the isolated antibody or antigen-binding fragment which includes a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method. In some embodiments of the methods described herein, the antibody or antigen-binding fragment is the isolated antibody or antigen-binding fragment that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 5, 2016 that has been assigned Accession No. PTA- 123090.

[00322] In some embodiments of the methods described herein, the antibody or antigen- binding fragment or the second antibody or antigen-binding fragment is the isolated antibody or antigen-binding fragment with a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 31, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 32, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 33, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to SEQ ID NO: 35, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 36, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 37 or the isolated antibody or antigen-b nding fragment that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 19, 2011 that has been assigned Accession No. PTA-11884.

[00323] In other embodiments, the antibody or antigen-binding fragment or the second antibody or antigen-binding fragment comprises a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method, or a isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody -producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123097. [00324] In other embodiments, the antibody or antigen-binding fragment or the second antibody or antigen-binding fragment comprises a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 55, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 56, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 62, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 63, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 64, wherein the CDRs are defined according to the IMGT method, or an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 58, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 59, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 65, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 66, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 64, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA- 123091, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00325] In other embodiments, the antibody or antigen-binding fragment or the second antibody or antigen-binding fragment comprises a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 84, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 85, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 86, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 90, a heavy chain

CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 91, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO:

92, wherein the CDRs are defined according to the IMGT method, or a isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 87, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 32, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 86, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 93, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 94, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 95, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA- 123098, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00326] In other embodiments, the antibody or antigen-binding fragment or the second antibody or antigen-binding fragment comprises an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 112, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 113, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 118, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 119, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 120, wherein the CDRs are defined according to the IMGT method, or an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 114, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 115, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 113, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 121, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 122, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 123, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody -producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123093, wherein the first isolated antibody or antigen- binding fragment is immobilized to a solid support and the second isolated antibody or antigen- binding fragment is labeled.

[00327] In other embodiments, the antibody or antigen-binding fragment or the second antibody or antigen-binding fragment comprises an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 55, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 140, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 141, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 145, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 146, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 147, wherein the CDRs are defined according to the IMGT method, or an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 58, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO:

142, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID

NO: 141, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 148, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 149, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 150, wherein the CDRs are defined according to the

KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123094, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00328] In other embodiments, the antibody or antigen-binding fragment or the isolated antibody or antigen-binding fragment comprises an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 55, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 56, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 57, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 168, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 169, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 170, wherein the CDRs are defined according to the IMGT method, or an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 58, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO:

59, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID

NO: 57, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ

ID NO: 171, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 172, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 173, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody -producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123092, wherein the first isolated antibody or antigen- binding fragment is immobilized to a solid support and the second isolated antibody or antigen- binding fragment is labeled.

[00329] In other embodiments, the antibody or antigen-binding fragment or the second antibody or antigen-binding fragment comprises an isolated antibody or antigen-binding fragment comprising a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 187, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 188, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 194, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 195, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 196, wherein the CDRs are defined according to the IMGT method, or a second isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 190, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 191, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 197, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 198, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 199, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123098, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00330] In other embodiments, the antibody or antigen-binding fragment or the second antibody or antigen-binding fragment comprises an isolated antibody or antigen-binding fragment comprising a light chain CDR1 amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 217, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 188, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 189, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 194, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 221, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 196, wherein the CDRs are defined according to the IMGT method, or an isolated antibody or antigen-binding fragment comprising a light chain CDRl amino acid sequence substantially the same as, or identical to SEQ ID NO: 218, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO:

191, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID

NO: 189, a heavy chain CDRl amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 197, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 222, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 199, wherein the CDRs are defined according to the

KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123095, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00331] In other embodiments, the antibody or antigen-binding fragment or the second antibody or antigen-binding fragment comprises an isolated antibody or antigen-binding fragment comprising a light chain CDRl amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 233, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 234, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 235, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 194, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 195, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 240, wherein the CDRs are defined according to the IMGT method, or a isolated antibody or antigen-binding fragment comprising a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO:

236, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID

NO: 237, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ

ID NO: 235, a heavy chain CDRl amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 241, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 198, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 242, wherein the CDRs are defined according to the

KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123101, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00332] In other embodiments, the antibody or antigen-binding fragment or the second antibody or antigen-binding fragment comprises an isolated antibody or antigen-binding fragment comprising a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 257, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 188, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 258, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 262, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 263, wherein the CDRs are defined according to the IMGT method, or an isolated antibody or antigen-binding fragment comprising a light chain CDRl amino acid sequence substantially the same as, or identical to SEQ ID NO: 259, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 191, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 258, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 264, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 265, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 266, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123096, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00333] In other embodiments, the antibody or antigen-binding fragment or the second antibody or antigen-binding fragment comprises an isolated antibody or antigen-binding fragment comprising a light chain CDRl amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to,

SEQ ID NO: 3, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method, or an isolated antibody or antigen-binding fragment with a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 115, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method, or the isolated antibody that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 4, 2016 that has been assigned Accession No. PTA-123100, wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

[00334] In some embodiments, the antibody or antigen-binding fragment is the isolated antibody or antigen-binding fragment with a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 31, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 32, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 33, a heavy chain CDRl amino acid sequence substantially the same as, or identical to SEQ ID NO: 35, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 36, and a heavy chain

CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 37 or the isolated antibody or antigen-binding fragment that is produced by antibody -producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va.

20110-2209) on May 19, 2011 that has been assigned Accession No. PTA-11884 and the second antibody or antigen-binding fragment is the isolated antibody or antigen-binding fragment with a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 1, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 2, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 8, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO:

9, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ

ID NO: 10, wherein the CDRs are defined according to the IMGT method, the isolated antibodies or antigen-binding fragment with a light chain CDRl amino acid sequence substantially the same as, or identical to, SEQ ID NO: 4, a light chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 5, a light chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 3, a heavy chain CDR1 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 11, a heavy chain CDR2 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 12, and a heavy chain CDR3 amino acid sequence substantially the same as, or identical to, SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method, or the antigen-binding fragment is the isolated antibody or antigen-binding fragment that is produced by antibody-producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 5, 2016 that has been assigned Accession No. PTA-123090.

[00335] Various combinations of the antibodies, or antigen-binding fragments thereof, may be used to quantify the amount of FRa in a sample. For example, any isolated antibody or antibody fragment in paragraphs [00320] through [00333] may be paired with any second isolated antibody or antibody fragment in paragraphs [00320] through [00333]. In preferred

embodiments, the isolated antibody or antigen-binding fragment and the second isolated antibody or antigen-binding fragment are different.

[00336] In some embodiments, the second antibody or antigen-binding fragment is immobilized to a solid support. In some embodiments, the second antibody or antigen-binding fragment is biotinylated and the solid support is coated with streptavidin, and the isolated antibody or antigen-binding fragment is immobilized to the solid support by the binding of biotin to streptavidin. In some embodiments, the presence of folate receptor alpha (FRa) in the sample is detected using western blot, immunohistochemistry, immunofluorescence, flow cytometry, radioimmunoassay, immunoprecipitation, electrochemiluminescence immunoassay (ECLIA), or ELISA. In some embodiments, the FRa -expressing cancer is ovarian cancer. In some embodiments, the method is conducted following treatment of the subject for cancer with MORAb-003.

[00337] In various embodiments of the described diagnostic methods a control sample is used. The control sample may be a positive or negative assay control that ensures the assay used is working properly; for example, an assay control of this nature might be commonly used for immunohistochemistry assays. Alternatively, the control sample may be a standardized control amount of FRa in a healthy subject. In some embodiments, the observed FRa levels of the tested subject may be compared with FRa levels observed in samples from control subjects known to have FRa-expressing cancer. [00338] The diagnostic methods provided herein also provide a basis upon which it may be possible to predict whether a subject has a relatively higher or lower likelihood of surviving 5 years following diagnosis. In some embodiments, the described method may be used to predict a favorable outcome for a subject having adenocarcinoma, wherein a favorable outcome is defined as having an increased 5-year survival rate. As data provided herein indicate, subjects determined to have stage I or stage II adenocarcinoma that does not express FRa are about 2 times more likely to die within five years than subjects determined to have stage I or stage II adenocarcinoma that does express FRa. Accordingly, the diagnostic methods described herein may be combined with this knowledge to allow for a method of predicting 5-year survivorship likelihood for subjects determined to have cancer. In some embodiments the method is used to predict the 5- year survivorship likelihood for subjects determined to have adenocarcinoma.

[00339] In some embodiments the described prognostic method will involve: contacting a biological sample of a subject with an FRa-specific antibody, or antigen-binding fragment thereof (such as those derivable from the antibodies and fragments provided in Table 1), quantifying the amount of FRa present in the sample that is bound by the antibody or antigen- binding fragment thereof, comparing the amount of FRa present in the sample to a known standard; and determining whether the subject's FRa levels indicate the presence of a FRa expressing cancer, thereby allowing for a prediction to be made as to the likelihood the subject will survive five years after being diagnosed with cancer. In some embodiments the subject is known to have or determined to have adenocarcinoma. In some embodiments the subject is a human.

[00340] In some embodiments the described methods involve assessing whether FRa- expressing cancer is progressing, regressing, or remaining stable by determining the amount of FRa-associated with a cell or tissue that is present in a test sample derived from the subject; and comparing the observed amount of FRa with the amount of FRa in a sample obtained from the subject, in a similar manner, at an earlier point in time, wherein a difference between the amount of FRa in the test sample and the earlier sample provides an indication of whether the cancer is progressing, regressing, or remaining stable. In this regard, a test sample with an increased amount of FRa, relative to the amount observed for the earlier sample, may indicate progression of a FRa-expressing cancer. Conversely, a test sample with a decreased amount of FRa, relative to the amount observed for the earlier sample, may indicate regression of a FRa-expressing cancer. Accordingly, a test sample with an insignificant difference in the amount of FRa, relative to the amount observed for the earlier sample, may indicate a state of stable disease for a FRa- expressing cancer. In some embodiments the amount of FRa in a sample derived from the subject is assessed by contacting the sample with an antibody that binds FRa such as the antibodies described herein. The sample assessed for the presence of FRa may be circulating cells, circulating tumor cells, cells that are not tissue associated (i.e., free cells), tissues (e.g., surgically resected tumor tissue, biopsies, including fine needle aspiration), histological preparations, and the like.

[00341] In some embodiments the described methods involve assessing whether FRa- expressing cancer is progressing, regressing, or remaining stable by determining the amount of FRa not associated with a cell or tissue that is present in a test sample derived from the subject; and comparing the observed amount of FRa with the amount of FRa in a sample obtained from the subject, in a similar manner, at an earlier point in time, wherein a difference between the amount of FRa in the test sample and the earlier sample provides an indication of whether the cancer is progressing, regressing, or remaining stable. In this regard, a test sample with an increased amount of FRa relative to the amount observed for the earlier sample, may indicate progression of a FRa-expressing cancer. Conversely, a test sample with a decreased amount of FRa relative to the amount observed for the earlier sample, may indicate regression of a FRa- expressing cancer. Accordingly, a test sample with an insignificant difference in the amount of FRa relative to the amount observed for the earlier sample, may indicate a state of stable disease for a FRa-expressing cancer. In some embodiments the amount of FRa in a sample derived from the subject is assessed by contacting the sample with an antibody that binds FRa, such as the antibodies described herein. The sample assessed for the presence of FRa may be urine, blood, serum, plasma, saliva, ascites, histological preparations, and the like.

Kits of the Invention

[00342] Provided herein are kits for detecting the presence of folate receptor alpha (FRa) in a biological sample. In some embodiments, the kit may contain the antibody or antigen- binding fragment of any one of the antibodies or antigen-binding fragments described herein. In some embodiments, the kit may contain an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by the antibody or antigen binding fragment of any one of the antibodies or antigen-binding fragments described herein. In some embodiments, the kit may contain an isolated antibody or antigen-binding fragment with a light chain CDRl comprising the amino acid sequence of SEQ ID NO: 31, a light chain CDR2 comprising the amino acid sequence of SEQ ID NO: 32, a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 33, a heavy chain CDRl comprising the amino acid sequence of SEQ ID NO: 35, a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 36, and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 37 or an isolated antibody or antigen- binding fragment that is produced by antibody -producing cells deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209) on May 19, 2011 that has been assigned Accession No. PTA-11884. In some embodiments, the kit may contain a vessel for containing the antibody, when not in use, and instructions for use of the antibody.

[00343] Also provided herein are kits for detecting the presence of folate receptor alpha (FRa) in a biological sample. In some embodiments, the kit may contain the antibody or antigen- binding fragment of any one of the antibodies or antigen-binding fragments described herein, wherein the antibody or antigen-binding fragment is affixed to a solid support. In some embodiments, the kit may contain an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by the antibody or antigen binding fragment of any one of the antibodies or antigen-binding fragments described herein wherein the antibody or antigen-binding fragment is affixed to a solid support. For example, the kit may contain the antibody or antigen- binding fragment described in paragraphs [0081] through [00102].

[00344] Also provided herein are kits for detecting the presence of folate receptor alpha (FRa) in a biological sample. In some embodiments, the kit may contain the antibody or antigen- binding fragment of any one of the antibodies or antigen-binding fragments described herein, wherein the antibody or antigen-binding fragment is affixed to a solid support. In some embodiments, the kit may contain an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by the antibody or antigen binding fragment of any one of the antibodies or antigen-binding fragments described herein wherein the antibody or antigen-binding fragment is affixed to a solid support. For example, the kit may contain the antibody or antigen- binding fragment described in paragraphs [0081] through [00102].

[00345] Also described herein are kits for detecting the presence of folate receptor alpha (FRa) in a biological sample. In some embodiments, the kit may contain the antibody or antigen- binding fragment of any one of the antibodies or antigen-binding fragments described herein, wherein the antigen-binding fragment is detectably labeled. In some embodiments, the kit may contain an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by the antibody or antigen binding fragment of any one of the antibodies or antigen- binding fragments described herein, wherein the antigen-binding fragment is detectably labeled. For example, the kit may contain the antibody or antigen-binding fragment described in paragraphs [0081] through [00102].

[00346] The provided antibody, or antigen-binding fragment, may be in solution;

lyophilized; affixed to a substrate, carrier, or plate; or conjugated to a detectable label. [00347] The described kits may also include additional components useful for performing the methods described herein. By way of example, the kits may comprise means for obtaining a sample from a subject, a control sample, e.g., a sample from a subject having slowly progressing cancer and/or a subject not having cancer, one or more sample compartments, and/or instructional material which describes performance of a method of the invention and tissue specific controls/standards.

[00348] The means for determining the level of FRa. can further include, for example, buffers or other reagents for use in an assay for determining the level of FRa. The instructions can be, for example, printed instructions for performing the assay and/or instructions for evaluating the level of expression of FRa.

[00349] The described kits may also include means for isolating a sample from a subject. These means can comprise one or more items of equipment or reagents that can be used to obtain a fluid or tissue from a subject. The means for obtaining a sample from a subject may also comprise means for isolating blood components, such as serum, from a blood sample.

Preferably, the kit is designed for use with a human subject.

[00350] The described kits may also include a blocking reagent that can be applied to a sample to decrease nonspecific binding of a primary or secondary antibody. An example of a blocking reagent is bovine serum albumin (BSA), which may be diluted in a buffer prior to use. Other commercial blocking reagents, such as Block Ace and ELISA Synblock (AbD serotec), Background Punisher (BIOCARE MEDICAL), and StartingBlock (Thermo Fisher Scientific) are known in the art. The described kits may also include a negative control primary antibody that does not bind to FRa sufficiently to yield a positive result in an antibody-based detection assay. In addition, the described kits may include a secondary antibody capable of binding to a FRa primary antibody, such antibody 24H8.D3, antibody 19D4.B7, antibody 24H8.F3, or antibody 1C6.E12.G8. In some embodiments the secondary antibody may be conjugated to a detectable label, such as horse radish peroxidase (HRP) or a fluorophore, to allow for detection of the primary antibody bound to a sample. The described kits may also include a colorimetric or chemiluminescent substrate that allows the presence of a bound secondary antibody to be detected on a sample. In some embodiments the colorimetric or chemiluminescent substrate may be 2,2'- azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS); 3,3',5,5'-Tetramethylbenzidine (TMB); 3,3'-Diaminobenzidine (DAB); SuperSignal (Thermo Fisher Scientific); ECL reagent (Thermo Fisher Scientific) or other such reagents known to those of ordinary skill in the art.

[00351] The following examples are provided to supplement the prior disclosure and to provide a better understanding of the subject matter described herein. These examples should not be considered to limit the described subject matter. It is understood that the examples and embodiments described herein are for illustrative purposes only and that various modifications or changes in light thereof will be apparent to persons skilled in the art and are to be included within the and can be made without departing from the true scope of the invention.

EXAMPLE 1 - Expression and Purification of Recombinant, Human Folate receptor alpha

[00352] To conduct the experiments associated with the studies described herein, several folate receptor alpha ("FRa" or "FOLRl")-expressing cell systems or lines were created to generate FRa-expressing cell substrates or to generate purified recombinant human FRa protein. One expression system used was a Sf9 insect cell line that expressed recombinant human FRa via baculovirus. This system was prepared using a human FRa sequence, containing a leader sequence optimized for insect cell expression, an N-terminal 6x histidine (6xhis) epitope tag, and the native GPI attachment site intact. The cells were then incubated in a 1L shake flask and log-phase cultures of Sf9 insect cells were infected with the recombinant baculovirus at a multiplicity of infection (MOI) of <1. Cells from 30L of culture were harvested, lysed and extracted 2x with IX phosphate-buffered saline (PBS) containing 10 mM 3-[(3- cholamidopropyl)dimethylammonio]-l-propanesulfonate (CHAPS). The NaCl concentration was adjusted to 300 mM and filtered through a 0.2 μιτι membrane. The clarified supernatant was purified by affinity chromatography, using IX PBS with 2M NaCl, 1 mM CHAPS, pH 7.4 as wash buffer, followed by elution with 10 mM 3-(N-morpholino)propanesulfonic acid (MOPS), 3M MgCh, 1 mM CHAPS, pH 6.8. Peak fractions were dialyzed extensively against IX PBS, pH 7.4, analyzed for purity by SDS-PAGE, quantitated by bicinchoninic acid assay (BCA) assay, aliquoted and stored at -80° Celsius.

[00353] A Chinese hamster ovary (CHO) cell line stably expressing and secreting human FRa was produced using a human folate receptor alpha (FRa) sequence, containing a human immunoglobulin kappa leader sequence and a C-terminal 6xhis epitope tag replacing the GPI attachment site. Once produced, the FRa-expressing CHO cells were grown at 25L-scale in wave bags. To purify the secreted FRa protein, cell supernatant was cleared of cellular debris by depth filtration and then concentrated 10-fold by tangential flow filtration and diafiltered into 50 mM sodium phosphate, 300 mM NaCl, 1 mM imidazole, pH 8.0. This was loaded onto a prepacked Talon® IMAC column using an FPLC. Unbound material was washed out using 50 mM sodium phosphate, 300 mM NaCl, 5 mM imidazole, pH 8.0 and bound protein was eluted using a linear gradient of 5 mM -100 mM imidazole in 50 mM sodium phosphate, 300 mM NaCl, pH 8.0. Peak fractions were dialyzed extensively against IX PBS, pH 7.4, analyzed for purity by SDS- PAGE, quantitated by BCA assay, aliquoted and stored at -80° Celsius.

[00354] A similar cell system was also produced for human folate receptor beta (FR{$), human folate receptor gamma (FRy), and human folate receptor delta (FR5). Briefly, constructs of either FR , FRy, or FR5 containing a human immunoglobulin kappa leader sequence and a C- terminal 6xhis epitope tag replacing the GPI attachment site, were used to transiently transfect 1L cultures of 293F cells. Recombinant FR proteins were purified as described above for human FRa.

[00355] A Chinese hamster ovary (CHO) cell line stably expressing and secreting a human mesothelin sequence, containing a human immunoglobulin kappa leader sequence and a C-terminal 6xhis epitope tag replacing the GPI attachment site, was also prepared, as mesothelin served as a negative control for many studies. Human mesothelin-expressing CHO cells were grown at 25L-scale in wave bags. To purify the secreted mesothelin protein, cell supematant was cleared of debris by hollow-fiber filtration and clarified supernatant was concentrated 10-fold by tangential flow filtration. Supernatant NaCl concentration was adjusted to 300 mM NaCl and 0.5 mM imidazole. This was loaded onto a pre-packed Talon® IMAC column using an FPLC.

Unbound material was washed out using 50 mM sodium phosphate, 300 mM NaCl, 3 mM imidazole, pH 8.0 and bound protein was eluted using 50 mM sodium phosphate, 300 mM NaCl, 150 mM imidazole, and pH 8.0. Peak fractions were dialyzed extensively against 50 mM potassium phosphate, pH 7.5. Ammonium sulfate was added to a final concentration of 1M, and final purification was then done on a pre-packed phenyl sepharose column using a step gradient of 1M - 0M ammonium sulfate in 50 mM potassium phosphate, pH 7.5. Peak fractions were dialyzed extensively against IX PBS, pH 7.4, analyzed for purity by SDS-PAGE, quantitated by BCA assay, aliquoted and stored at -80° Celsius.

EXAMPLE 2 - Production of Purified Reduced and Alkylated FRa

[00356] Efforts were undertaken to produce a reduced and alkylated antigenic form of FRa. To reduce the protein, purified FRa was concentrated to 2 mg/mL in phosphate buffered saline (pH 7.4) using centrifugal filters (Amicon Ultra, 3 kDa MW limit). The protein concentration was determined using a BCA assay (Thermo Scientific). The resultant FRa was diluted 1 : 1 in 8M urea/ PBS to generate a final concentration of 1 mg/mL FRa in PBS containing 4M urea. Dithiothreitol solution (500 mM in PBS) was added to a final concentration of 10 mM. The solution was incubated at 65° Celsius for one hour, and cooled to room temperature. [00357] Next 1M of iodoacetamide solution in phosphate buffer saline was added into the reduced folate receptor solution to a final concentration of 10 mM, and the reaction was kept in dark at room temperature for 30 minutes. The protein remained soluble under these conditions. The final reduced FRa to be used for immunization was stored in phosphate buffer saline containing 4M of urea, lOmM of DTT, and 10 mM of iodoacetamide.

[00358] FIG. 1 shows the differential migration of native FRa protein and a reduced and alkylated form of the protein analyzed by SDS-PAGE under non-reducing conditions.

EXAMPLE 3 - Production of Hybridomas to FRa

[00359] Eight week old female Balb/c mice were immunized with hexa-histidine tagged FRa protein (n=5) or reduced and alkylated FRa protein (n=5). Initial intraperitoneal

immunizations administered on day 0 comprised 50μg of the respective immunogen mixed 1 : 1 (v:v) with complete Freund's adjuvant (Rockland, Cat# D614-0050). Mice were then boosted with 50μg immunogen mixed 1 : 1 (v:v) with incomplete Freund's adjuvant (Rockland, Cat# D615-0050) administered intraperitoneally 14 days later and every 21 days thereafter. Blood samples were collected from immunized mice 24 days after the initial immunization and every 21 days thereafter.

[00360] Collected blood samples were analyzed by direct enzyme-linked immunoassay (EIA) against FRa. Plates were coated with FRa protein (ΙΟΟμΙ of a ^g/mL solution in PBS, 0.02 M potassium phosphate, 0.15 M Sodium Chloride, pH 7.2) and incubated overnight at 4°C, washed with PBS containing 0.2% Tween®-20 (PBST; Rockland, Cat# MB-075-1000) and blocked with 3% fish gel (Sigma) for lhr at room temperature. A 3-fold dilution series of individual mouse serum samples were allowed to bind for lhr at room temperature, plates were then washed 3 times with PBST and subsequently probed with an HRP -conjugated rabbit-anti- mouse antibody (Rockland, Cat#610-4320) at 1 :2500 for 30 minutes at 37°C. TMB substrate (Rockland, Cat# TMBE-100) was added and the reaction was stopped after 30 minutes by addition of lOOmL of 1M HC1 prior to absorbance reading at 450nm (Microplate Reader

"Benchmark"; Biorad). All samples were counter-screened against hexa-histidine tagged recombinant mesothelin (mesothelin-His6) protein as a negative control.

[00361] Spleens from mice showing the highest antigen-specific titers were harvested and hybridomas were prepared by electrofusion (Hybrimune™ Model CEEF-50B Waveform

Generator; Cellectis, Romainville, France) of splenocytes with Sp2/0 Agl4 myeloma cells (ATTC

CRL1581). Subsequently, hybridoma supernatants were screened by ELISA against FRa and recombinant Mesothelin-His6 as described above to select positive parental fusion cell lines. [00362] Selected parental cell lines determined to produce antibodies reactive to recombinant human FRa (rhFRa) were then subcloned by limiting dilution. The antibodies produced by these cells were then retested for FRa binding and isotyped using the Clonetyping™ System (SouthernBiotech, Birmingham, AL). Supernatants from these clones were further screened by direct ELISA against three additional isoforms of the human folate receptor (FR , FRy and FR5) to determine receptor specificity. Plates were coated overnight with ΙΟΟμί of a ^g/mL solution of the respective FR isoform at 4°C, washed with PBS containing 0.2%

Tween®-20 (Rockland, Cat# MB-075-1000) and blocked with 3% fish gel (Sigma). A 3-fold dilution series of culture supernatants was allowed to bind for lhr at room temperature, before plates were washed and probed with an HRP-conjugated anti-mouse antibody as described above. Clones producing antibodies reactive to FR , FRy or FR5 were not selected for further analysis.

[00363] Hybridoma clones 24H8.D3, 1C6.E12.G8, 1D2.D8.G10, 6A2.G7, 19D2.G9, 26A9.C4, 2F11.F8, 5C12.H8, 24H8.F3, 28H12.G9, 30G6.G6.G4.E9, and 1A8.G11.E7, generated from the mice immunized with either native/non-reduced or reduced/alkylated folate receptor alpha as listed in Table 3, were selected for further analysis. On May 4, 2016, the clones were deposited with the American Type Culture Collection (10801 University Blvd. Manassas, Virginia 20110-2209) and were assigned the following ATCC accession numbers: 24H8.D3 (PTA-123090), 1C6.E12.G8 (PTA-123091), 1D2.D8.G10 (PTA-123098), 6A2.G7 (PTA- 123093), 19D2.G9 (PTA-123094), 26A9.C4 (PTA-123092), 2F11.F8 (PTA-123098), 5C12.H8 (PTA-123095), 24H8.F3 (PTA-123097), 28H12.G9 (PTA-123101) , 30G6.G6.G4.E9 (PTA- 123096), and 1A8.G11.E7 (PTA-123100).

EXAMPLE 4 - Production of Purified Monoclonal Antibodies

[00364] Selected cell lines were tested for mycoplasma using a mycoplasma test kit (Rockland, Cat# MAB-012) before seeding into 1L roller bottles containing serum free medium (Invitrogen, Cat# 12045-076) and 5% low IgG FBS (0. l ug/ml) (Gibco, Cat# 16250-078) at 0.5xl0 ⁵ cells/mL. Cultures were allowed to grow at 37°C for either 14 or 21 days, after which supernatant was harvested and concentrated approximately 10-fold through a 50kDa filtration membrane (Spectrum Labs, Rancho Dominguez CA) and then purified using protein A chromatography (Rockland, Cat# PA50-00-0025). Bound antibody was eluted with 0.1M sodium citrate, pH 3.5/4.5 depending on antibody isotype, and buffer was exchanged against PBS by dialysis using a 12-14kDa membranous tubing (Spectrum Labs, Rancho Dominguez CA).

Purified antibody was sterile filtered using a 0.22μιη Express™ PLUS Stericups (Millipore, Billerica MA) and stored at 4°C for further testing.

[00365] Efforts were undertaken to sequence the heavy and light chains of the hybridoma clones. First, total RNA was isolated from the hybridoma cell line (cell pellets of 1 x 10 ³ to 1 x 10 ⁵ cells each) using the RNAqueous® kit (Ambion) according to the manufacturer's protocol. RNA was quantified using a NanoDrop™ 8000 spectrophotometer (Thermo Scientific).

[00366] Isolated RNA was then amplified via multiplex RT-PCR, performed in triplicate for each hybridoma with a Mastercycler® EP Gradient Thermocycler (Eppendorf). First, two separate gene-specific cDNA amplifications were performed for each hybridoma (≤^g RNA/reaction) to determine which Ig heavy and light chain genes were used during Ig rearrangement. Each cocktail consisted of unique family-specific primers designed to anneal to any of the potential murine Ig V gene families (IgHv, IgKv) and Ig constant region genes (IgHcGamma, IgKc). cDNA generation and amplification was performed using Superscript® III One-Step RT-PCR System with Platinum® Taq High Fidelity (Invitrogen) under the following conditions: 55°C for 30 minutes and 95°C for 2 minutes, followed by 40 cycles of 95°C for 1 minute, 55°C for 1 minute, 68°C for 1 minute, and a final 68°C for 10 minutes completion step. DNA products were electrophoresed on a 2% agarose gel. Appropriate bands were excised and gel purified using the QIAquick® Gel Extraction Kit (Qiagen) following the manufacturer's protocol. Purified DNA was submitted for sequencing (GENEWIZ, Inc., South Plainfield, NJ) to determine the germline gene segments expressed by each hybridoma.

[00367] Further RT-PCR analysis suited to the particular genes identified for the hybridomas was then performed using the same RNA source as above and gene-specific primers (in contrast to family-specific primers used in the multiplex RT-PCR mixture). To facilitate cloning, amplified Ig cDNAs were placed into an In-Fusion (IF) expression vector, each gene- specific primer also contained vector-compatible linker sequences which would enable homologous crossover. All other reagents and thermocycler conditions are the same as those used for the multiplex RT-PCR experiments, described above.

EXAMPLE 5 - MORAb-003 Interference in the Control folate receptor alpha assay

[00368] The previously described ECL assay disclosed in U.S. Patent No. 8,475,795 for the detection of folate receptor assay in serum, plasma and urine was demonstrated to be interfered with in the presence of the therapeutic monoclonal antibody farletuzumab (MORAb- 003), thereby obviating its use to monitor therapeutic response, i.e. in the presence of therapeutic MORAb-003. Table 4 shows the partem of interference by MORAb-003 at two concentrations, for the assay configured with MAb 9F3.H9.H3.H3.B5.G2 ("9F3") as capture and MAb 24F12.B1 ("24F12") as detection across the standard curve. As disclosed in U.S. Patent No. 8,475,795, antibodies 9F3 and 24F12 were deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Virginia 20110-2209) on May 19, 2011 and were assigned ATCC accession numbers PTA-11887 and PTA-11886, respectively. The assay demonstrates a

MORAb-003 concentration-dependent interference pattern. As such, additional MAbs were screened to identify a capture/detect combination insensitive to endogenous MORAb-003.

Table 4: MORAb-003 Interference in the Control folate receptor alpha assay

EXAMPLE 6 - Selecting MAb pairs with the Least Interference from MORAb-003

Antibody Pair Screening

[00369] Antibody pairs were assessed to determine which pair gave good assay performance and exhibited the least interference by MORAb-003. Screening was performed on thirteen monoclonal antibodies such that all antibodies were screened as capture and detection antibodies. An antibody pair disclosed in U.S. Patent No. 8,475,795 - 26B3.F2 (capture) and 19D4.B7 (detection) - was used as a positive control. Antibodies 26B3.F2 and 19D4.B7 were previously deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Virginia 20110-2209) on May 19, 2011 and were assigned Accession Nos. PTA-11885 and PTA-11884, respectively. Serum samples provided by MSD were used. The serum samples were incubated with 10μg/mL MORAb-003 overnight and tested at 1 :20 dilution. Serum samples were incubated in diluent overnight as a control and tested at 1 :20 and 1 :80 dilutions. The calibrator was also treated with 10μg/mL MORAb-003 overnight. 24H8.D3 was tested as both a capture and detection antibody, and was identified as promising due to high signal to background (S/B) levels.

[00370] FIG. 2A shows the light intensity count resulting from pairwise combinations of thirteen capture antibodies and thirteen detection antibodies. FIG. 2B shows the average signal to background (S/B) values resulting from the pairwise combinations of thirteen capture antibodies and thirteen detection antibodies.

[00371] The effect of MORAb-003 interference was assessed at 10μg/mL. Antibody pairs were assessed to determine which antibody combination exhibited the least interference by MORAb-003 based on a low signal.

[00372] All combinations were masked where the specific signal was below 1000. MAb 30G6.G6.G4.E9 was not able to detect endogenous levels of antigen. Percent Drug Interference was calculated using the formula % Drug Interference = (Signal with Drug - Blank) / (Signal without Drug - Blank). FIG. 3A shows percent interference/drug suppression after adding 10μg/mL MORAb-003 for the pairwise combinations of thirteen capture antibodies and thirteen detection antibodies in a control calibrator solution containing recombinant purified FRa at a concentration of 500pg/mL. FIG. 3B shows percent interference/drug suppression after adding 10μg/mL MORAb-003 for the pairwise combinations of thirteen capture antibodies and thirteen detection antibodies in serum samples. The positive control is located in the upper right corner for comparison. Percent interference = (Signal with MORAb-003 - Blank) / (Signal without MORAb-003 - Blank).

EXAMPLE 7: Assessment and Screening of Antibody Pairs Based on Dilution Linearity of

Two Serum Samples and Standard Curve Performance

[00373] Dilution linearity profiles and standard curve performance of various antibody pairs listed below were assessed using two serum samples. The antibodies assessed were 1A8.G11.E7, 24H8.D3, 9F3, 19D4.B7 and 19D2.G9. FIG. 4 shows examples of dilution linearity when using 24H8.D3 and 19D4.B7 as both the capture and detection antibody as compared to other antibody pairs. Dilution adjusted concentrations were normalized to the concentration at 1 :20 dilution and the grayed sections are antibody combinations not considered during the screening.

[00374] Next, the standard curve performance and slope were assessed for the selected antibody pairs. The final selected antibody pair and best configuration for the assay included 24H8.D3 as the capture antibody and 19D4.B7 as the detector based on the superior slope (1.09) as shown in FIG. 5A and FIG. 5B. 1A8.G11.E7 and 24H8.D3 likely recognize the same or similar epitope because they behave the same and do not work with one another. FIG. 5A depicts graphs of signal plotted against concentration for a defined capture antibody and paired with one of four detection antibodies. FIG. 5B shows the standard curve and hill slope data for the tested antibody pairs. 19D4.B7 worked better as a detector than when used as a capture.

EXAMPLE 8: Final Folate receptor alpha Electrochemiluminescence (ECL) Assay

Protocol/Configuration

[00375] Small spot Streptavidin (ss-SAV) plates were blocked with 150μί of Meso Scale Discovery® (MSD) Blocker A at room temperature with shaking for 30 minutes. Each well was coated with 25μ1. of biotin-conjugated 24H8.D3 capture antibodies at 0.5μg/mL. The plates were incubated at room temperature with shaking for 1 hour. The plates were washed three times with PBST. Next, 25μ1. of the sample/calibrator was added to each well. The samples were incubated at room temperature with shaking for 2 hours. The plates were then washed three times with PBST. 25μΙ, of SULFO-TAG (from Meso Scale Diagnostics, LLC) conjugated 19D4.B7 detection antibody was added to each well at a concentration of ^g/mL. The plates were incubated at room temperature for 1 hour with shaking. The plates were washed three times with PBST. The plates were read with 2X Read Buffer T immediately. The standards were generated using recombinant purified FRa for a standard curve with a zero calibrator, as depicted in Table 5.

Table 5: FRa Calibrator Concentrations

EXAMPLE 9 - Folate receptor alpha Assay Performance and Sample Matrix Assessments Reference Range

[00376] 40 human patient samples (20 healthy normal patients and 20 ovarian cancer patients) were used to establish the reference ranges for the FRa ECL assay. Each patient provided four sample types (serum, plasma, first morning urine and spot urine) to assess performance and suitability of each sample type. Three patients did not have the spot urine sample available. Samples were spiked with 100 μg/mL MORAb-003. To control the study, samples were spiked with assay diluent and run in parallel with the MORAb-003 drug-treated samples.

[00377] Table 6 shows the light intensity counts of eight FRa standard samples with concentrations ranging from 0 pg/mL to 5000 pg/mL over six consecutive runs. The data, also depicted in graphical form in FIG. 6, demonstrates that the standard curve exhibited good reproducibility over the range of the curve for all six runs.

Table 6: FRa Standard Curve Reproducibility

[00378] Dilution Linearity was assessed using serum and urine samples. Five serum and five urine samples were tested at six different dilutions. Serum samples fell within the range of the standard curve while urine samples displayed slightly higher FRa levels (FIG. 7A - 7D). FIG. 7A shows a graph of the light intensity counts (y-axis) of eight standard FRa samples and five serum samples (x-axis) at 10, 20, 40, 80, 160 and 320-fold dilutions. FIG. 7B shows a graph of the percent normalized recovery (y-axis) plotted against the fold dilution for all five serum samples (x-axis) and demonstrates good dilution linearity with approximately 10% variance. FIG. 7C shows a graph of the light intensity counts (y-axis) of eight standard FRa samples and five urine samples (x-axis) at 10, 20, 40, 80, 160 and 320-fold dilutions. FIG. 7D shows a graph of the percent normalized recovery (y-axis) plotted against the fold dilution for all five urine samples (x-axis) and demonstrates acceptable dilution linearity (within approximately 20% variance).

Folate receptor alpha Spike Recovery

[00379] Five serum and five urine samples were spiked with high (H), medium (M) and low (L) levels of the FRa calibrator and run in comparison to diluent as a control. In FIGS. 8A and FIG. 8B, the percent normalized recovery, as compared to expected recovery values, was plotted on the y-axis and spike levels were plotted on the x-axis. FIG. 8A shows the results from the five serum samples and FIG. 8B slows the results from the five urine samples. Slightly elevated but acceptable recovery values were seen in the serum samples.

Folate receptor alpha Assay Precision (% CV)

[00380] The precision or coefficient of variance was assessed by testing all serum, plasma and urine samples in duplicate. Serum and plasma results were consistent with CVs generally < 5%. Urine CV% results were generally higher than serum and plasma and more varied across the detectable range of the curve, as depicted in FIG. 9.

EXAMPLE 10 - Folate receptor alpha ECL Assay Performance in the Presence of MORAb-003

[00381] The effect of MORAb-003 on the performance of the FRa ECL assay was assessed in serum and plasma. FRa levels were tested in samples with or without MORAb-003 spiked into patient samples at a level of 100μg/mL, which is the approximate expected level in patients receiving treatment. The percent inhibition was calculated as % Inhibition =

(Diluent/Drug) / Diluent where drug is MORAb-003. The assay exhibits minimal interference in serum and plasma samples with serum being the best sample matrix with less interference. As depicted in FIGS. 10A - IOC, the percent inhibition median serum value was 3% with a range of - 10% to 14%. The plasma median serum value was 4% with a range of -32% to 27%. Sample #DLSO-015 was omitted from the correlation analysis as inhibition in serum was 21% and inhibition in plasma was 10%. FIG. 10A illustrates the percent inhibition of FRa levels in plasma and serum samples with and without 100μg/mL MORAb-003. FIG. 1 OB is a plot of FRa levels in serum or plasma samples treated with 100μg/mL MORAb-003 (y-axis) against FRa levels in control, diluent-treated, serum or plasma samples (x-axis), and FIG. IOC is an expanded view of the low, boxed, end of the curve in FIG. 10B. R ² values for serum and plasma are also provided in FIG. IOC.

Sample Matrix Testing and Performance with Addition of MORAb-003

[00382] To evaluate the performance of serum, plasma and urine in the FRa ECL assay, 40 human patient samples (20 healthy normal patients and 20 ovarian cancer patients) were identified. Each patient had four sample types assessed with the exception of three patients without spot urine samples (serum, plasma, first morning urine and spot urine). To assess performance and suitability of each sample type and the possible interference of MORAb-003 in serum and plasma samples, the serum and plasma samples were run with and without the addition of MORAb-003 along with the standard curve.

[00383] The serum and plasma samples were detectable and in the range of the curve, however, urine results were generally higher than serum and plasma values and a few urine samples had values that were above the range of the curve at the dilution used in this assessment. Serum and plasma exhibited excellent concordance and little change in values with the addition of MORAb-003. The results of these analyses are depicted in Table 7 and graphically in FIG. 11. The graph in FIG. 11 plots light intensity count for eight standard samples, serum and plasma samples with and without MORAb-003, and spot and first morning (AM) urine samples.

Table 7: Serum and Plasma Concordance in the Presence of MORAb-003

EXAMPLE 11: Analytical Characterization of Assay Antibodies

[00384] Selection of antibodies used in assay development included an analysis of the physical properties of each antibody. The antibodies were processed to ensure they were in the optimal buffer for the intended use as either a capture or detection antibody before analysis. The antibodies were evaluated using the following methods: (1) capillary isoelectric focusing (cIEF) to establish the pi peak and range and the peak profile; (2) dynamic light scattering (DLS) to assess aggregation; (3) experion automated electrophoresis (reducing and non-reducing) to assess purity and establish a heavy to light chain ratio. The results from the analyses are depicted in FIG. 12A and FIG. 12B. L/P represents labels of biotin per protein.

EMBODIMENTS

The following list of embodiments is intended to complement, rather than displace or supersede, the previous desriptions.

Embodiment 1. An isolated antibody, or antigen-binding fragment thereof, specific for folate receptor alpha (FRa) comprising:

a. a light chain CDR1 comprising the amino acid sequence of SEQ ID NO: 1, a light chain CDR2 comprising the amino acid sequence of SEQ ID NO: 2, a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 3, a heavy chain CDR1 comprising the amino acid sequence of SEQ ID NO: 8, a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 9, and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method; or

b. a light chain CDR1 comprising the amino acid sequence of SEQ ID NO: 4, a light chain CDR2 comprising the amino acid sequence of SEQ ID NO: 5, a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 3, a heavy chain CDR1 comprising the amino acid sequence of SEQ ID NO: 11, a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 12, and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method.

Embodiment 2. The isolated antibody or antigen-binding fragment of embodiment 1, wherein the antibody is a murine antibody.

Embodiment 3. The isolated antibody or antigen-binding fragment of embodiment 1 or 2, wherein the antibody isotype is IgG.

Embodiment 4. The isolated antibody or antigen-binding fragment of any one of embodiments 1 to 3, wherein the antibody is chimeric.

Embodiment 5. The isolated antibody or antigen-binding fragment of any one of embodiments 1 to 4, wherein the antibody is humanized. Embodiment 6. The isolated antibody or antigen-binding fragment of any one of embodiments 1 to 5, wherein:

a. the antibody or antigen-binding fragment of (a) has a light chain variable region

comprising an amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 6 and a heavy chain variable region that is at least 90% identical to the amino acid sequence of SEQ ID NO: 14; or

b. the antibody or antigen-binding fragment of (b) has a light chain variable region

comprising an amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 6 and a heavy chain variable region that is at least 90% identical to the amino acid sequence of SEQ ID NO: 14.

Embodiment 7. The isolated antibody or antigen-binding fragment of embodiment 6, wherein the light chain variable region has the amino acid sequence of SEQ ID NO: 6 and the heavy chain variable region has the amino acid sequence of SEQ ID NO: 14.

Embodiment 8. An isolated antibody, or antigen-binding fragment thereof, specific for folate receptor alpha (FRa) comprising a light chain variable region that has the amino acid sequence of SEQ ID NO: 6 and a heavy chain variable region that has the amino acid sequence of SEQ ID NO: 14.

Embodiment 9. An isolated antibody, or antigen-binding fragment thereof, specific for folate receptor alpha (FRa) comprising a light chain that has the amino acid sequence of SEQ ID NO: 7 and a heavy chain that has the amino acid sequence of SEQ ID NO: 15.

Embodiment 10. An isolated antibody specific for folate receptor alpha (FRa) produced by the cell line deposited with the ATCC comprising accession number PTA-123090.

Embodiment 11. An isolated polynucleotide comprising the nucleotide sequence of SEQ ID NO:

21 and SEQ ID NO: 29.

Embodiment 12. An isolated polynucleotide comprising the nucleotide sequence of SEQ ID NO:

22 and SEQ ID NO: 30. Embodiment 13. An isolated polynucleotide encoding an antibody or antigen-binding fragment comprising a light chain variable region and a heavy chain variable region wherein the light chain variable region comprises the amino acid sequence of SEQ ID NO: 6 and the heavy chain variable region comprises the amino acid sequence of SEQ ID NO: 14.

Embodiment 14. An isolated polynucleotide encoding an antibody comprising a light chain and a heavy chain wherein the light chain comprises the amino acid sequence of SEQ ID NO: 7 and the heavy chain comprises the amino acid sequence of SEQ ID NO: 15.

Embodiment 15. An isolated polynucleotide sequence encoding an antibody or antigen-binding fragment specific for folate receptor alpha (FRa), wherein:

a. a light chain CDR1 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 1, a light chain CDR2 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 2, a light chain CDR3 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 3, a heavy chain CDR1 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 8, a heavy chain CDR2 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 9, and a heavy chain CDR3 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method; or b. a light chain CDR1 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 4, a light chain CDR2 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 5, a light chain CDR3 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 3, a heavy chain CDR1 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 11, a heavy chain CDR2 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 12, and a heavy chain CDR3 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method.

Embodiment 16. An isolated polynucleotide comprising the nucleotide sequences of:

a. SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 23, SEQ ID NO:

24, and SEQ ID NO 25; or

b. SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 18, SEQ ID NO: 26, SEQ ID NO:

27, and SEQ ID NO 28. Embodiment 17. An isolated polynucleotide sequence encoding an antibody light chain or antigen-binding fragment specific for folate receptor alpha (FRa), wherein:

a. the light chain CDR1 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 1, the light chain CDR2 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 2, and the light chain CDR3 of the encoded antibody comprises the amino acid sequence SEQ ID NO: 3, wherein the CDRs are defined according to the IMGT method; or

b. the light chain CDR1 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 4, the light chain CDR2 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 5, and the light chain CDR3 of the encoded antibody comprises the amino acid sequence SEQ ID NO: 3, wherein the CDRs are defined according to the KABAT method.

Embodiment 18. An isolated polynucleotide sequence encoding an antibody heavy chain or antigen-binding fragment specific for folate receptor alpha (FRa), wherein:

a. the heavy chain CDR1 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 8, the heavy chain CDR2 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 9, and the heavy chain CDR3 of the encoded antibody comprises the amino acid sequence SEQ ID NO: 10, wherein the CDRs are defined according to the IMGT method; or b. the heavy chain CDR1 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 11, the heavy chain CDR2 of the encoded antibody comprises the amino acid sequence of SEQ ID NO: 12, and the heavy chain CDR3 of the encoded antibody comprises the amino acid sequence SEQ ID NO: 13, wherein the CDRs are defined according to the KABAT method.

Embodiment 19. A vector comprising the isolated polynucleotide of any one of embodiments 11 to 18.

Embodiment 20. A recombinant cell comprising the vector of embodiment 19.

Embodiment 21. The recombinant cell of embodiment 20, wherein the cell is a eukaryotic cell, a yeast cell, a plant cell, or a bacterium. Embodiment 22. The recombinant cell of embodiment 21, wherein the eukaryotic cell is a CHO cell.

Embodiment 23. A method of detecting folate receptor alpha (FRa) in a biological sample, comprising exposing the sample to the antibody or antigen-binding fragment of any one of embodiments 1 to 10, and detecting FRa.

Embodiment 24. The method of embodiment 23, wherein the biological sample is derived from urine, blood, serum, plasma, saliva, ascites, circulating cells, circulating tumor cells, cells that are not tissue associated, tissues, surgically resected tumor tissue, biopsies, fine needle aspiration samples, or histological preparations.

Embodiment 25. The method of embodiment 23 or 24, wherein the biological sample is derived from a human or nonhuman primate.

Embodiment 26. The method of any one of embodiments 23 to 25, wherein the antibody is labeled.

Embodiment 27. The method of embodiment 26, wherein the label is a radiolabel, an epitope tag, biotin, a chromophore label, a fluorophore label, an electrochemiluminescence (ECL) label, or an enzyme.

Embodiment 28. The method of embodiment 27, wherein the electrochemiluminescence (ECL) label is a sulfo-tag.

Embodiment 29. The method of any one of embodiments 23 to 28, further comprising exposing the sample to a second antibody or antigen-binding fragment of any one of embodiments 1 to 10.

Embodiment 30. The method of embodiment 29, wherein the second antibody or antigen- binding fragment is immobilized to a solid support.

Embodiment 31. The method of embodiment 30, wherein the second antibody or antigen- binding fragment is biotinylated and the solid support is coated with streptavidin, and the isolated antibody or antigen-binding fragment is immobilized to the solid support by the binding of biotin to streptavidin.

Embodiment 32. The method of any one of embodiments 23 to 31, wherein the presence of folate receptor alpha (FRa) in the sample is detected using western blot, immunohistochemistry, immunofluorescence, flow cytometry, radioimmunoassay, immunoprecipitation,

electrochemiluminescence immunoassay (ECLIA), or ELISA.

Embodiment 33. The method of any one of embodiments 23 to 32, wherein the sample is diluted prior to detecting folate receptor alpha (FRa) in the sample.

Embodiment 34. The method of any one of embodiments 23 to 33, wherein the sample is centrifuged, vortexed, or both, prior to detecting folate receptor alpha (FRa) in the sample.

Embodiment 35. The method of any one of embodiments 23 to 34, wherein the level of folate receptor alpha (FRa) in the sample is quantified.

Embodiment 36. The method of any one of embodiments 23 to 35, wherein the sample is exposed to MORAb-003 prior to detecting folate receptor alpha (FRa) in the sample.

Embodiment 37. A method of detecting folate receptor alpha (FRa) in a biological sample, comprising:

a. exposing the sample to a first isolated antibody or antigen-binding fragment of embodiment 1(a), embodiment 1(b) or embodiment 10 and a second isolated antibody or antigen-binding fragment with a light chain CDR1 comprising the amino acid sequence of SEQ ID NO: 31, a light chain CDR2 comprising the amino acid sequence of SEQ ID NO: 32, a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 33, a heavy chain CDR1 comprising the amino acid sequence of SEQ ID NO: 35, a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 36, and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 37 or the isolated antibody with the accession number PTA-11884, or

b. a first isolated antibody or antigen-binding fragment with a light chain CDR1 comprising the amino acid sequence of SEQ ID NO: 31, a light chain CDR2 comprising the amino acid sequence of SEQ ID NO: 32, a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 33, a heavy chain CDR1 comprising the amino acid sequence of SEQ ID NO: 35, a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 36, and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 37 or the isolated antibody with the accession number PTA-11884 and a second isolated antibody or antigen-binding fragment of embodiment 1(a), embodiment 1(b) or embodiment 10;

wherein the first isolated antibody or antigen-binding fragment is immobilized to a solid support and the second isolated antibody or antigen-binding fragment is labeled.

Embodiment 38. The method of embodiment 37, wherein the biological sample is derived from urine, blood, serum, plasma, saliva, ascites, circulating cells, circulating tumor cells, cells that are not tissue associated, tissues, surgically resected tumor tissue, biopsies, fine needle aspiration samples, or histological preparations.

Embodiment 39. The method of embodiment 37 or 38, wherein the biological sample is derived from a human or nonhuman primate.

Embodiment 40. The method of any one of embodiments 37 to 39, wherein the sample is diluted prior to detecting FRa in the sample.

Embodiment 41. The method of any one of embodiments 37 to 40, wherein the sample is centrifuged, vortexed, or both, prior to detecting FRa in the sample.

Embodiment 42. The method of any one of embodiments 37 to 41, wherein the label is a radiolabel, an epitope tag, biotin, a chromophore label, a fluorophore label, an

electrochemiluminescence (ECL) label, or an enzyme.

Embodiment 43. The method of embodiment 42, wherein the electrochemiluminescence (ECL) label is a sulfo-tag.

Embodiment 44. The method of any one of embodiments 37 to 43, wherein the first isolated antibody or antigen-binding fragment is biotinylated and the solid support is coated with streptavidin, and the first isolated antibody or antigen-binding fragment is immobilized to the solid support by the binding of biotin to streptavidin.

Embodiment 45. The method of any one of embodiments 37 to 44, wherein the presence of folate receptor alpha (FRa) in the sample is detected using western blot, immunohistochemistry, immunofluorescence, flow cytometry, radioimmunoassay, immunoprecipitation,

electrochemiluminescence immunoassay (ECLIA), or ELISA.

Embodiment 46. The method of any one of embodiments 37 to 45, wherein the level of FRa in the sample is quantified.

Embodiment 47. The method of any one of embodiments 37 to 46, wherein the sample is exposed to MORAb-003 prior to detecting folate receptor alpha (FRa) in the sample.

Embodiment 48. A method of diagnosing a folate receptor alpha (FRa)-expressing cancer in a subject, comprising:

a. exposing the biological sample of the subject to:

i. the antibody or antigen-binding fragment of any one of embodiments 1 to 10, or

ii. an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by the antibody or antigen binding fragment of any one of embodiments 1 to 10,

b. quantifying the amount of FRa present in the sample that is bound by the antibody or antigen-binding fragment;

c. comparing the amount of FRa present in the sample to a known standard; and d. determining whether the subject's FRa levels fall within the levels of FRa associated with cancer.

Embodiment 49. A method of monitoring a folate receptor alpha (FRa)-expressing cancer in a subject, comprising:

a. exposing the biological sample of the subject to:

i. the antibody or antigen-binding fragment of any one of embodiments 1 to 10, or ii. an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by the antibody or antigen binding fragment of any one of embodiments 1 to 10,

b. quantifying the amount of FRa present in the sample that is bound by the antibody or antigen-binding fragment;

c. comparing the amount of FRa present in the sample to either i. a known standard, or

ii. a biological sample obtained from the subject at an earlier point in time; and

d. determining whether the subject's FRa levels are indicative of cancer progression, regression or stable disease.

Embodiment 50. A method of treating a folate receptor alpha (FRa)-expressing cancer in a subject, comprising:

a. exposing the biological sample of the subject to:

i. the antibody or antigen-binding fragment of any one of embodiments 1 to 10, or

ii. an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by the antibody or antigen binding fragment of any one of embodiments 1 to 10,

b. quantifying the amount of FRa present in the sample that is bound by the antibody or antigen-binding fragment;

c. comparing the amount of FRa present in the sample to a known standard; d. determining whether the subject's FRa levels fall within the levels of FRa associated with cancer; and

e. administering to the subject, or prescribing, a treatment for the cancer.

Embodiment 51. The method of any one of embodiments 48 to 50, wherein the antibody or antigen-binding fragment is immobilized to a solid support.

Embodiment 52. The method of any one of embodiments 48 to 50, wherein the antibody or antigen-binding fragment is biotinylated and the solid support is coated with streptavidin, and the isolated antibody or antigen-binding fragment is immobilized to the solid support by the binding of biotin to streptavidin. Embodiment 53. The method of any one of embodiments 48 to 52, wherein the step of exposing a biological sample of the subject to:

a. the antibody or antigen-binding fragment of any one of embodiments 1 to 10, or b. an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by the antibody or antigen binding fragment of any one of embodiments 1 to 10,

further comprises exposing the biological sample of the subject to a second antibody or antigen- binding fragment.

Embodiment 54. The method of embodiment 53, wherein the second antibody or antigen- binding fragment comprises a light chain CDRl comprising the amino acid sequence of SEQ ID NO: 31, a light chain CDR2 comprising the amino acid sequence of SEQ ID NO: 32, a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 33, a heavy chain CDRl comprising the amino acid sequence of SEQ ID NO: 35, a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 36, and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 37 or the isolated antibody or antigen-binding fragment with the accession number PTA-11884.

Embodiment 55. The method of embodiment 53 or 54, wherein the second antibody or antigen- binding fragment is labeled.

Embodiment 56. The method of embodiment 55, wherein the label is a radiolabel, an epitope tag, biotin, a chromophore label, a fluorophore label, an electrochemiluminescence (ECL) label, or an enzyme.

Embodiment 57. The method of embodiment 56, wherein the electrochemiluminescence (ECL) label is a sulfo-tag.

Embodiment 58. The method of any one of embodiments 48 to 57, wherein the presence of folate receptor alpha (FRa) in the sample is detected using westem blot, immunohistochemistry, immunofluorescence, flow cytometry, radioimmunoassay, immunoprecipitation,

electrochemiluminescence immunoassay (ECLIA), or ELISA. Embodiment 59. The method of any one of embodiments 48 to 58, wherein the FRa -expressing cancer is ovarian cancer.

Embodiment 60. The method of any one of embodiments 48 to 59, wherein the method is conducted following treatment of the subject for cancer with MORAb-003.

Embodiment 61. A kit for detecting the presence of folate receptor alpha (FRa) in a biological sample, comprising:

c. the antibody or antigen-binding fragment of any one of embodiments 1 to 10, or d. an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by the antibody or antigen binding fragment of any one of embodiments 1 to 10, and

e. an isolated antibody or antigen-binding fragment with a light chain CDR1 comprising the amino acid sequence of SEQ ID NO: 31, a light chain CDR2 comprising the amino acid sequence of SEQ ID NO: 32, a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 33, a heavy chain CDR1 comprising the amino acid sequence of SEQ ID NO: 35, a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 36, and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 37 or an isolated antibody or antigen-binding fragment with the accession number PTA-11884; and

a vessel for containing the antibody, when not in use, and instructions for use of the antibody.

Embodiment 62. A kit for detecting the presence of folate receptor alpha (FRa) in a biological sample, comprising:

f. the antibody or antigen-binding fragment of any one of embodimetns 1 to 10, or g. an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by the antibody or antigen binding fragment of any one of embodiments 1 to 10, and

h. an isolated antibody or antigen-binding fragment with a light chain CDR1 comprising the amino acid sequence of SEQ ID NO: 31, a light chain CDR2 comprising the amino acid sequence of SEQ ID NO: 32, a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 33, a heavy chain CDR1 comprising the amino acid sequence of SEQ ID NO: 35, a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 36, and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 37 or an isolated antibody or antigen-binding fragment with the accession number PTA-11884

wherein the antibody or antigen-binding fragment is affixed to a solid support.

Embodiment 63. A kit for detecting the presence of folate receptor alpha (FRa) in a biological sample, comprising:

i. the antibody or antigen-binding fragment of any one of embodiments 1 to 10, or j. an antibody or antigen-binding fragment capable of binding the epitope of FRa that is bound by the antibody or antigen binding fragment of any one of embodiments 1 to

10, and

k. an isolated antibody or antigen-binding fragment with a light chain CDRl comprising the amino acid sequence of SEQ ID NO: 31, a light chain CDR2 comprising the amino acid sequence of SEQ ID NO: 32, a light chain CDR3 comprising the amino acid sequence of SEQ ID NO: 33, a heavy chain CDRl comprising the amino acid sequence of SEQ ID NO: 35, a heavy chain CDR2 comprising the amino acid sequence of SEQ ID NO: 36, and a heavy chain CDR3 comprising the amino acid sequence of SEQ ID NO: 37 or an isolated antibody or antigen-binding fragment with the accession number PTA-11884

wherein the antigen-binding fragment is detectably labeled.