IMMUNOGENIC FUSION PROTEINS FOR THE TREATMENT OF CANCER RELATED APPLICATIONS

[0001] This application claims the benefit of U.S. Provisional Application No.

62/146,626, filed on April 13, 2015, and U.S. Provisional Application No. 62/146,654, filed April 13, 2015 and U.S. Provisional Application No. 62/263, 174, filed December 4, 2015. The entire teachings of the above applications are incorporated herein by reference.

GOVERNMENT SUPPORT

[0002] This invention was made with government support under contract W81XWH-12- 1-0439 from the U.S. Army Medical Research Acquisition Activity (USAMRAA). The government has certain rights in the invention.

BACKGROUND

[0003] Other than skin cancer, prostate cancer is the most common cancer in American men. According to the American Cancer Society, an estimated 220,800 new cases of prostate cancer and 27,540 deaths from prostate cancer will occur in 2015 in the United States alone. About 1 man in 7 will be diagnosed with prostate cancer during his lifetime. Advances in cancer diagnosis and treatment during the last decade have increased treatment options but have not provided curative treatments for patients with metastatic prostate cancer. Additional therapies are needed for these patients.

SUMMARY OF THE INVENTION

[0004] Disclosed herein are fusion proteins comprising an epidermal growth factor receptor variant III (EGFRvIII) polypeptide and a synovial sarcoma, X breakpoint 2 (SSX2) polypeptide. In some embodiments, the fusion proteins can comprise one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10. In other embodiments the fusion proteins can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in amino acid residues 89 to 475 of SEQ ID NO:4.

[0005] Also provided are nucleic acid molecules encoding the EGFRvIII-SSX2 fusion proteins. In some embodiments, the nucleic acid molecule can comprise one or more EGFRvIII polynucleotides that are at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO: 5 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to the SSX2 polynucleotide as set forth in SEQ ID NO:9. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[0006] Disclosed herein are fusion proteins comprising an EGFRvIII polypeptide and a prostatic acid phosphatase (PAP) polypeptide. In some embodiments, the fusion proteins can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, or iii) 99% identical iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP33.386 as set forth in amino acid residues 89 to 606 SEQ ID NO: 12. In other embodiments, the fusion protein can comprise one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14.

[0007] Also provided are nucleic acid molecules encoding the EGFRvIII-PAP fusion proteins. In some embodiments, the nucleic acid molecule can comprise one or more EGFRvIII polynucleotides that are at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO: 5 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to the PAP 33.386 polynucleotide as set forth in SEQ ID NO: 13. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[0008] Disclosed herein are fusion proteins comprising an EGFRvIII polypeptide, an NK3 homeobox 1 (NKX3.1) polypeptide, and a prostate-specific membrane antigen (PSMA) polypeptide. In some embodiments, the fusion proteins can comprise one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 n _-23 4 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%. identical to PSMAi _-20 , ₄₄ - ₁₃₈ , ₁ 69-750 as set forth in SEQ ID NO:20. In other embodiments, the fusion proteins can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5- KX3. 1 ii _-2 34-PSMAi _-20j 44-i3 ₈ , 169-750 as set forth in amino acid residues 89 to 1177 of SEQ ID NO:23. In other embodiments, the fusion proteins can comprise one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6, a KX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to KX3. l(R41 G)n _-23 4 as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi. _20; 44.i _{38; 169} - ₇₅₀ as set forth in SEQ ID NO:20. In other embodiments, the fusion proteins can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

EGFRVIIIX5-NKX3.1(R41 G) _{I I-234} -PSMA _I-2 O _{J 44} . _{138, 1} 69-750 as set forth in amino acid residues 89 to 1177 of SEQ ID NO: 16.

[0009] Also provided are nucleic acid molecules encoding the EGFRvIII-NKX3.1 -PSMA fusion proteins. In some embodiments, the nucleic acid molecule can comprise one or more EGFRvIII polynucleotides that are at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5, a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3.I _n . ₂₃ 4 polynucleotide as set forth in SEQ ID NO:24, and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to the PSMA ]. ₂ o _, 44.138 _, 109-750 as set forth in SEQ ID NO: 19. In some aspects, the nucleic acid molecule is operably linked to a promoter. In other embodiments, the nucleic acid molecules can comprise one or more EGFRvIII polynucleotides that are at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5, a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3.1(R41G)n. ₂₃ 4 polynucleotide as set forth in SEQ ID NO: 17, and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to the PSMA1-20, 44-138, w- 750 as set forth in SEQ ID NO: 19. In some aspects, the nucleic acid molecule is operably linked to a promoter. [0010] Disclosed herein are fusion proteins comprising an KX3.1 polypeptide and a PAP polypeptide. In some embodiments, the fusion proteins can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to KX3.1-PAP ₃₃ -386 as set forth in amino acid residues 89 to 678 of SEQ ID NO:27. In some embodiments, the fusion proteins can comprise a KX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to KX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33-386 as set forth in SEQ ID NO: 14.

[0011] Also provided are nucleic acid molecules encoding the NKX3.1-PAP fusion proteins. In some embodiments, the nucleic acid molecules can comprise a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3.1 polynucleotide as set forth in SEQ ID NO:28 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the PAP ₃₃ -386 polynucleotide as set forth in SEQ ID NO: 13. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[0012] Disclosed herein are host cells comprising one or more of the disclosed nucleic acid molecules. In some embodiments, the host cells can comprise one or more nucleic acid molecules comprising a nucleic acid sequence encoding:

a) an EGFRvIII-SSX2 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

b) an EGFRvIII-PAP _33-386 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33-386 as set forth in SEQ ID NO: 14;

c) an EGFRvIII-NKX3.1 ₁₁ . ₂₃₄ -PSMA ₁ . _20; 44-m _, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 n _-23 4 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20; 4-138, 169-750 as set forth in SEQ ID NO:20;

an EGFRvIII-NKX3.1(R41G)ii _-2 34-PSMAi _-2 o _; 44-138, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1(R41G)n. ₂₃₄ as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-2 o _; 44.i _38; 169-750 as set forth in SEQ ID NO:20;

a NKX3.1-PAP _33-3 86 fusion protein, wherein the fusion protein comprises a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33-386 as set forth in SEQ ID NO: 14; an ActAN100*-SSX2 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10; or an ActAN100-PAP _30-3 86 fusion protein, wherein the fusion protein comprises an ActANlOO polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to amino acid residues 1 to 100 of SEQ ID NO:33 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _30-38 6 as set forth in amino acid residues 103-459 of SEQ ID NO:33;or

h) any combination thereof.

[0013] In some aspects, the one or more nucleic acid molecules listed in a)-h) are operably linked to a promoter.

[0014] Methods of eliciting an immune response in a subject are also provided. In some embodiments, the methods can comprise administering to the subject a composition comprising a host cell, said host cell comprising one or more nucleic acid molecules, said nucleic acid molecules comprising a nucleic acid sequence encoding:

a) an EGFRvIII-SSX2 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

b) an EGFRvIII-PAP _33-3 86 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33-386 as set forth in SEQ ID NO: 14;

c) an EGFRvIII-NKX3.1 ₁₁ . ₂₃₄ -PSMA ₁ . _{20; 44} . _138; 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 n _-234 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _{-20; 44-} i _38; 169-750 as set forth in SEQ ID NO:20;

d) an EGFRvIII-NKX3. l(R41G)ii _-234 -PSMAi _-2 o, ₄ 4-i38, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1(R41G)n. 234 as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-2 o, 44-138, 169-750 as set forth in SEQ ID NO:20;

e) a NKX3. l-PAP ₃₃ .386 fusion protein, wherein the fusion protein comprises a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14; f) an ActAN100*-SSX2 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

g) an ActAN100*-PAP ₃ o-386 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to ActANlOO* as set forth as SEQ ID NO:2 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%> identical to PAP30-386 as set forth in amino acid residues 103-459 of SEQ ID NO:33; or

h) any combination thereof.

[0015] In some aspects, the one or more nucleic acid molecules listed in a)-h) are operably linked to a promoter.

[0016] Provided are methods of eliciting an immune response in a subject comprising, administering to the subject a composition comprising a host cell, wherein the host cell expresses one or more fusion proteins comprising: an EGFRvIII-SSX2 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

an EGFRvIII-PAP33.386 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33- 386 as set forth in SEQ ID NO: 14;

an EGFRvIII-NKX3.1 ₁₁ . ₂₃₄ -PSMA ₁ . _{20; 44} . _138; 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ΝΚΧ3.1 ιι _-234 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20; 4-138, 169-750 as set forth in SEQ ID NO:20;

an EGFRvIII-NKX3.1(R41G)ii _-2 34-PSMAi _-20 , 44-158, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1(R41G)n _-234 as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20 , ₄ 4-i ₃₈ , 169-750 as set forth in SEQ ID NO:20; a NKX3.1-PAP _33-386 fusion protein, wherein the fusion protein comprises a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to KX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14; f) an ActAN100*-SSX2 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

g) an ActAN100*-PAP ₃ o-386 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%> identical to PAP30-386 as set forth in amino acid residues 103-459 of SEQ ID NO:33; or

h) any combination thereof.

[0017] Further provided are methods of increasing expression of an antigenic

polypeptide. In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule, said nucleic acid molecule comprising a nucleic acid sequence encoding:

a) an EGFRvIII-SSX2 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

b) an EGFRvIII-PAP ₃₃ .3 ₈₆ fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -3 ₈ 6 as set forth in SEQ ID NO: 14; an EGFRvIII- KX3.111.234-PSMA1.20, 44-138, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 n. ₂₃ 4 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi-20, 44-138, 169-750 as set forth in SEQ ID NO:20;

an EGFRvIII-NKX3.1(R41G)ii.234-PSMAi.2o, 44-138, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1(R41G)n. 234 as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMA1.20, 44-138, 169-750 as set forth in SEQ ID NO:20;

a NKX3. l-PAP33.386 fusion protein, wherein the fusion protein comprises a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP33-386 as set forth in SEQ ID NO: 14; an ActAN100*-SSX2 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

an ActAN100*-PAP ₃ o-386 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _30- 386 as set forth in amino acid residues 103-459 of SEQ ID NO:33; or

h) any combination thereof.

[0018] In some aspects, the one or more nucleic acid molecules listed in a)-h) are operably linked to a promoter.

[0019] Disclosed herein are methods of treating cancer in a subject in need thereof, said methods comprising administering to the subject a therapeutically effective amount of a composition comprising a host cell, wherein the host cell comprises one or more of the disclosed nucleic acid molecules. In some embodiments, the methods can comprise administering to the subject a therapeutically effective amount of a composition comprising a host cell, wherein the host cell comprises one or more nucleic acid molecules comprising a nucleic acid sequence encoding:

a) an EGFRvIII-SSX2 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

b) an EGFRvIII-PAP33.386 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP33-386 as set forth in SEQ ID NO: 14; c) an EGFRvIII-NKX3.1 ₁₁ . ₂₃₄ -PSMA ₁ . _20; 44-138, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 n _-23 4 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi.20, 44-138, 169-750 as set forth in SEQ ID NO:20;

an EGFRvIII- KX3.1(R41G)ii _-2 34-PSMAi _-2 o _; 44-138, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1(R41G)n- 234 as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-2 o, 44-138, 169-750 as set forth in SEQ ID NO:20;

a NKX3. l-PAP ₃₃ .386 fusion protein, wherein the fusion protein comprises a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14; an ActAN100*-SSX2 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

an ActAN100-PAP ₃ o-386 fusion protein, wherein the fusion protein comprises an ActANlOO polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to ActANl OO as set forth in to amino acid residues 1 to 100 of SEQ ID NO:33 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to PAP30-386 as set forth in amino acid residues 103-459 of SEQ ID NO:33; or any combination thereof. [0020] In some aspects, the one or more nucleic acid molecules listed in a)-h) are operably linked to a promoter.

[0021] Provided are methods of treating cancer in a subject in need thereof, said method comprising administering to the subject a therapeutically effective amount of a composition comprising a host cell, wherein the host cell expresses one or more fusion proteins comprising:

a) an EGFRvIII-SSX2 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

b) an EGFRvIII-PAP33.386 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33-386 as set forth in SEQ ID NO: 14;

c) an EGFRvIII-NKX3.1 ₁₁ . ₂₃₄ -PSMA ₁ . _{20; 44} . _138, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 n _-234 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20; 44-158, 169-750 as set forth in SEQ ID NO:20;

d) an EGFRvIII-NKX3. l(R41G)ii _-23 4-PSMAi _-2 o _{; 44-} i _38; 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1(R41G)n _-234 as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20, 44-m _, 169-750 as set forth in SEQ ID NO:20; e) a NKX3. l-PAP ₃₃ .386 fusion protein, wherein the fusion protein comprises a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

NKX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14; f) an ActAN100*-SSX2 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10; or g) an ActAN100-PAP _30- 386 fusion protein, wherein the fusion protein comprises an ActANlOO polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to

ActANl OO as set forth in to amino acid residues 1 to 100 of SEQ ID NO:33 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₀ - 386 as set forth in amino acid residues 103-459 of SEQ ID NO:33; or h) any combination thereof.

BRIEF DESCRIPTION OF THE DRAWINGS

[0022] The summary, as well as the following detailed description, is further understood when read in conjunction with the appended drawings. For the purpose of illustrating the disclosed compositions and methods, there are shown in the drawings exemplary

embodiments of the compositions and methods; however, the compositions and methods are not limited to the specific embodiments disclosed. In the drawings:

[0023] FIG. 1 illustrates an exemplary schematic diagram of the BH5290 strain, with five cancer antigenic polypeptides expressed as three separate immunogenic fusion proteins. [0024] FIG .2 illustrates the expression of immunogenic fusions comprising the

KX3.1 (R41 G) variation.

[0025] FIG. 3A-FIG. 3E illustrate immunogenicity of exemplary immunogenic fusion proteins comprising the KX3.1(R41G) variation. (FIG. 3A) SSX2-specific immunity; (FIG. 3B) PAP-specific immunity; (FIG. 3C) KX3.1 -specific immunity; (FIG. 3D)

PSMA-specific immunity; and (FIG. 3E) EGFRvIII-specific immunity.

[0026] FIG. 4 illustrates the protective immunity of vaccination with BH5290 against a wild type Listeria challenge.

[0027] FIG. 5A-FIG. 5B illustrate the expression of SSX2 when fused to EGFRvIII. (A) Exemplary bacterial strains used to examine SSX2 expression in the presence of EGFRvIII. To assess the impact of inclusion of EGFRvIIIx5 on antigen expression, matched SSX2 expression cassettes differing only in the presence of EGFRvIIIx5 were introduced at the tRNA ^Arg locus of the same Lm background that expressed an ActAN100*- KX3.1-PAP ₃ 3-386 fusion protein from the inlB locus. BH4598 contained the first cassette - ActAN100*-SSX2, and BH4602 contained the second cassette - ActAN100*-EGFRvIIIx5-SSX2 (FIG. 5A). All expression cassettes utilized the actA promoter. (FIG. 5B) Intracellular western blot results. Lane 1 : Lml l (negative control), lane 2: BH4598 (ActAN100*-SSX2), lane 3 : BH4602 (ActAN100*-EGFRvIIIx5-SSX2).

[0028] FIG. 6 illustrates SSX2 immune responses when EGFRvIIIx5 is part of the immunogenic fusion protein.

[0029] FIG. 7A-FIG. 7B illustrate PAP expression when fused to multiple copies of EGFRvIII. (A) Six PAP expression cassettes were constructed that vary in the copy number of the EGFRvIII repeat sequence included in the construct. All constructs were integrated at the tRNA ^Avg locus of Lml 1 resulting in six Lm vaccine strains: BH2868, PL1631, PL1629, PL1627, PL1625, and PL1623. (B) Expression was evaluated by intracellular western. Lane 1 : Lml 1 (no expression cassette); Lane 2: BH2868 expresses ActAN100-PAP _33-386 ; Lane 3 : PL1631 expresses ActAN100*-EGFRvIIIxl-PAP _33-386 ; Lane 4: PL1629 expresses

ActAN100*-EGFRvIIIx2-PAP _33-386 ; Lane 5: PL1627 expresses ActAN100*-EGFRvIIIx3- PAP _33-386 ; Lane 6: PL1625 expresses ActAN100*-EGFRvIIIx4-PAP _33-386 ; Lane 7: PL1623 expresses ActAN100*-EGFRvIIIx5-PAP _33-386 .

[0030] FIG. 8 illustrates PAP-specific immunogenicity when fused to multiple copies of EGFRvIII. Six PAP expressing Lm strains with the variation in EGFRvIII copy number (BH2868, PL1631, PL1629, PL1627, PL1625, and PL1623) were tested for induction of T cell responses.

DETAILED DESCRIPTION OF THE INVENTION

[0031] A description of example embodiments of the invention follows.

[0032] The disclosed compositions and methods may be understood more readily by reference to the following detailed description taken in connection with the accompanying figures, which form a part of this disclosure. It is to be understood that the disclosed compositions and methods are not limited to the specific compositions and methods described and/or shown herein, and that the terminology used herein is for the purpose of describing particular embodiments by way of example only and is not intended to be limiting of the claimed compositions and methods.

[0033] Unless specifically stated otherwise, any description as to a possible mechanism or mode of action or reason for improvement is meant to be illustrative only, and the disclosed compositions and methods are not to be constrained by the correctness or incorrectness of any such suggested mechanism or mode of action or reason for

improvement.

[0034] Throughout this text, the descriptions refer to compositions and methods of using said compositions. Where the disclosure describes or claims a feature or embodiment associated with a composition, such a feature or embodiment is equally applicable to the methods of using said composition. Likewise, where the disclosure describes or claims a feature or embodiment associated with a method of using a composition, such a feature or embodiment is equally applicable to the composition.

[0035] It is to be appreciated that certain features of the disclosed compositions and methods which are, for clarity, described herein in the context of separate embodiments, may also be provided in combination in a single embodiment. Conversely, various features of the disclosed compositions and methods that are, for brevity, described in the context of a single embodiment, may also be provided separately or in any subcombination.

[0036] As used herein, the singular forms "a," "an," and "the" include the plural.

[0037] The following abbreviations are used throughout the disclosure: EGFRvIII (Epidermal Growth Factor Receptor variant III neoantigen junction region); EGFRvIIIx5 (5 copies of EGFRvIII); SSX2 (synovial sarcoma, X breakpoint 2) (accession no. Q16385); NKX3.1 (NK3 homeobox 1 polypeptide) (accession no. Q99801); PSMA (prostate-specific membrane antigen) (accession no. Q04609); PAP (prostatic acid phosphatase) (accession no. P15309); Lm {Listeria monocytogenes); LADD (double-deleted Listeria monocytogenes).

[0038] The delta symbol (Δ or ".DELTA.") refers to a deletion. For example, "AactA" (or ".DELTA.actA") means that all, or part, of the actA gene is deleted.

[0039] The term "subject" as used herein refers to a human or non-human organism. Thus, the methods and compositions described herein are applicable to both human and veterinary disease. In certain embodiments, subjects are "patients," i.e., living humans that are receiving medical care for a disease or condition. This includes persons with no defined illness who are being investigated for signs of pathology. Preferred are subjects who have malignancy expressing one or more, and preferably each of, EGFRvIII, SSX2, KX3.1, PMSA, and PAP. In certain embodiments, the subject is suffering from prostate cancer, and preferably metastatic prostate cancer.

[0040] The terms "percent identical," "sequence identity," and "percent identity" as used herein refers to the percent of amino acids that are the same {i.e. identical) between two or more polypeptides. Sequence identity between two or more polypeptides can be determined by aligning the amino acid sequences of the polypeptides and scoring the number of positions in the aligned polypeptides that contain the same amino acid residue and comparing that to the number of positions in the aligned polypeptides that differ. Polypeptides can differ at a position, for example, by containing a different amino acid {i.e. substitution or mutation) or by lacking an amino acid {i.e. amino acid insertion or amino acid deletion in one or both of the polypeptides). Sequence identity can be calculated by dividing the number of positions that contain the same amino acid residue by the total number of amino acid residues in the polypeptide. Percent identity, for example, can be calculated by dividing the number of positions that contain the same amino acid residue by the total number of amino acid residues in the polypeptide and multiplying by 100.

[0041] "Immunogenic fragment thereof includes portions of fusion proteins that are able to elicit an immunogenic response in a subject. In some aspects, the immunogenic fragment comprises, consists of, or consists essentially of the fusion protein. In other aspects, the immunogenic fragment comprises, consists of, or consists essentially of signal sequence(s)-fusion protein.

[0042] As used herein, "fusion protein" refers to a protein made from the joining of two or more polypeptides. Fusion proteins can be generated by chemically conjugating the polypeptides. Preferably, fusion proteins are generated by genetic fusion, in which nucleic acid molecules encoding the individual polypeptides are joined in-frame, such that transcription and translation of the nucleic acid molecules generates a single protein comprising the individual polypeptides. The disclosed fusion proteins may have one or more linker residues between the polypeptides.

[0043] As used herein, "signal sequence" refers to polypeptide sequences, and nucleotide sequences encoding the same, that function to drive secretion of the fusion protein. The signal sequence is operably linked to the polypeptide(s) comprising the fusion protein and is translational reading frame with the polypeptide(s) comprising the fusion protein. "Signal sequences" can also be refered to as "secretory signal sequences."

[0044] As used herein, "operably linked" refers to the juxtaposition of control sequences, such as a promoter ribosome binding site in a manner that the normal function of the components is maintained. "Control sequences" typically refer to DNA sequences necessary for the expression of an operably linked coding sequence in the host organism. The control sequences can include a promoter, a ribosome binding site and, optionally, a Shine/Dalgarno sequence. Thus, a coding sequence "operably linked" to an encoded signal sequence refers to a configuration wherein the coding sequence is joined to the signal sequence in such a manner that the signal peptide is processed by the host cell and the processed protein is secreted. A signal sequence operably linked to a promoter is joined to the promoter in such a manner that the transcription and translation of the secretion signal sequence is controlled by the promoter, ribosome binding site, and Shine/Dalgarno sequence if required.

[0045] As used herein "i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical" encompasses at least 90% identical, 91% identical, 92% identical, 93% identical, 94% identical, 95% identical, 96% identical, 97% identical, 98% identical, 99% identical, or 100% identical to the reference item (e.g., a biological sequence).

[0046] For EGFRvIII polypeptides and immunogenic fusion proteins containing the same, any sequence variability described herein must occur outside of amino acid residues 7 to 14 of SEQ ID NO:6 (EEKKGNYV). In other words, sequence variability can occur in amino acid residues 1 to 6 of SEQ ID NO: 6 (PASRAL) or immunogenic fusion proteins containing the same and/or amino acid residues 15 to 21 of SEQ ID NO:6 (VTDHGSC) or immunogenic fusion proteins containing the same. For example, an EGFRvIII polypeptide comprising an amino acid sequence at least 90% identical to SEQ ID NO:6, encompasses amino acid sequences that are 90% identical, 91% identical, 92% identical, 93% identical, 94% identical, 95% identical, 96% identical, 97% identical, 98% identical, 99% identical, or 100% identical to SEQ ID NO: 6, wherein the variability occurs in amino acid residues 1 to 6 or 15 to 21 of SEQ ID NO:6. Accordingly, each EGFRvIII polypeptide and immunogenic fusion protein containing the same will contain amino acid residues 7 to 14 of SEQ ID NO: 6 (EEKKGNYV).

[0047] EGFRvIII polypeptides can be adjusted in length to include shorter portions of SEQ ID NO:6. For example, in some embodiments, the EGFRvIII polypeptide can comprise, consist, of, or consist essentially of an amino acid sequence at least 90% identical to amino acid residues 6 to 18 of SEQ ID NO:6. In some embodiments, the one or more copies of EGFRvIII polypeptide can comprise, consist, of, or consist essentially of an amino acid sequence at least 90% identical to amino acid residues 6 to 14 of SEQ ID NO:6. As described above, the variability in these shorter polypeptides will occur in amino acid residues 1 to 6 or 15 to 21 of SEQ ID NO:6. Accordingly, for an amino acid sequence at least 90% identical to amino acid residues 6 to 18 of SEQ ID NO:6, the variability can occur at amino acid residue 6 or 15 to 18 of SEQ ID NO:6. For an amino acid sequence at least 90%) identical to amino acid residues 6 to 14 of SEQ ID NO: 6, the variability can occur at amino acid residue 6.

[0048] Throughout the disclosure, immunogenic fusion proteins comprising, and nucleic acids encoding immunogenic fusion proteins that comprise, one or more EGFRvIII polypeptide are described. The EGFRvIII polypeptide can be encoded by any one of the EGFRvIII nucleotide sequences provided in Table 1. Accordingly, throughout the disclosure, when the EGFRvIII polynucleotide is refered as being "at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 5" (the consensus sequence in Table 1), it is intended to include: at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:42; at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:43; at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:44; at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:45;

and/or at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to SEQ ID NO:46. Similarly, the nucleotide sequences encoding the various immunogenic fusion proteins can comprise any one of SEQ ID NOs:42-46. Therefore, each EGFRvIII- containing immunogenic fusion protein provided herein can be encoded by a nucleic acid molecule, wherein the nucleic acid molecule comprises one or more polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:42, at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:43, at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:44, at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:45, and/or at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:46. In some aspects, the nucleic acid molecule is operably linked to a promoter.

Table 1

[0049] Immunogenic fusion proteins

[0050] Disclosed herein are immunogenic fusion proteins and nucleic acid molecules encoding said fusion proteins. Exemplary immunogenic fusion proteins are provided in Tables 2 and 3. Table 1 provides exemplary combinations of antigens expressed by the fusion proteins. Table 3 provides exemplary expression cassettes, bacterial strains, and amino acid ranges of the various fusions proteins. Table 2

[0051] The immunogenic fusion proteins can comprise any of the above combinations of antigens (i.e. EGFRvIII, SSX2, KX3.1, PAP, PSMA). The antigens described herein may include a sequence that is a MHC class I epitope or a MHC class II epitope from the full- length protein sequence.

[0052] EGFR is a receptor tyrosine kinase critical for cell growth and survival. The EGFR gene is frequently overexpressed or mutated in human cancers, including head and neck, colon, pancreas, breast, ovary, kidney, and malignant gliomas. EGFR receptor variant III (EGFRvIII) results from a 267 amino acid deletion of exons 2 to 7 and the fusion of exon 1 with exon 8, yielding a tumor-specific peptide with a novel glycine at the junction.

EGFRvIII exhibits constitutive, ligand-independent signaling. In one embodiment, a described EGFRvIII polynucleotide comprises a sequence encoding at least one MHC class I epitope or at least one MHC class II epitope. Similarly, the EGFRvIII polypeptides described herein include at least one MHC class I epitope or at least one MHC class II epitope. The sequence of the N-terminal 10 residues of the EGFRvIII mutation is LEEKKGNYVV, as set forth in SEQ ID NO:61.

[0053] SSX2 belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. The SSX2 gene, and also the SSX1 and SSX4 family members, have been involved in

t(X; 18)(pl 1.2;ql 1.2) translocations that are characteristically found in all synovial sarcomas. This translocation results in the fusion of the synovial sarcoma translocation gene on chromosome 18 to one of the SS genes on chromosome X. The encoded hybrid proteins are likely responsible for transforming activity. Alternative splicing of this gene results in multiple transcript variants. In one embodiment, a described SSX2 polynucleotide comprises a sequence encoding at least one MHC class I epitope or at least one MHC class II epitope. Similarly, the SSX2 polypeptides described herein include at least one MHC class I epitope or at least one MHC class II epitope. A SSX2 sequence (Swiss Prot entry Q16385) is set forth as SEQ ID NO: 62:

10 2 0 3 0 4 0 50

MNGDDAFARR PTVGAQI PEK IQKAFDDIAK YFSKEEWEKM KASEKI FYVY

6 0 70 8 0 90 100

MKRKYEAMTK LGFKATLPPF MCNKRAEDFQ GNDLDNDPNR GNQVERPQMT

110 12 0 13 0 14 0 150

FGRLQGI SPK IMPKKPAEEG NDSEEVPEAS GPQNDGKELC PPGKPTTSEK

16 0 170 18 0

IHERSGPKRG EHAWTHRLRE RKQLVI YEEI SDPEEDDE

[0054] NKX3.1 (NK3 homeobox 1 polypeptide) (accession no. Q99801) is a transcription factor, which binds preferentially the consensus sequence 5'-TAAGT[AG]-3' and can behave as a transcriptional repressor. NKX3.1 plays an important role in normal prostate

development, regulating proliferation of glandular epithelium and in the formation of ducts in prostate. In one embodiment, a described NKX3.1 polynucleotide comprises a sequence encoding at least one MHC class I epitope or at least one MHC class II epitope. Similarly, the NKX3.1 polypeptides described herein include at least one MHC class I epitope or at least one MHC class II epitope. The human canonical sequence of NKX3.1 (Swiss Prot entry Q99801) is set forth as SEQ ID NO:29:

10 2 0 3 0 4 0 50

MLRVPEPRPG EAKAEGAAPP TPSKPLTSFL IQDI LRDGAQ RQGGRTSSQR

6 0 70 8 0 90 100

QRDPEPEPEP EPEGGRSRAG AQNDQLSTGP RAAPEEAETL AETEPERHLG

110 12 0 13 0 14 0 150

SYLLDSENTS GALPRLPQTP KQPQKRSRAA FSHTQVI ELE RKFSHQKYLS

16 0 170 18 0 190 2 00

APERAHLAKN LKLTETQVKI WFQNRRYKTK RKQLSSELGD LEKHSSLPAL

210 22 0 23 0

KEEAFSRASL VSVYNSYPYY PYLYCVGSWS PAFW

[0055] PSMA (prostate-specific membrane antigen) (accession no. Q04609) has both folate hydrolase and N-acetylated-alpha-linked-acidic dipeptidase (NAALADase) activity. PSMA as a preference for tri-alpha-glutamate peptides. In the intestine, PSMA is required for the uptake of folate; in the brain, PSMA modulates excitatory neurotransmission through the hydrolysis of the neuropeptide, N-aceylaspartylglutamate (NAAG), thereby releasing glutamate. PSMA is also involved in prostate tumor progression. In one embodiment, a described PSMA polynucleotide comprises a sequence encoding at least one MHC class I epitope or at least one MHC class II epitope. Similarly, the PSMA polypeptides described herein include at least one MHC class I epitope or at least one MHC class II epitope. The human canonical sequence of PSMA (Swiss Prot entry Q04609) is set forth as SEQ ID NO:63 :

10 20 30 40 50

MWNLLHETDS AVATARRPRW LCAGALVLAG GFFLLGFLFG WFIKSSNEAT

60 70 80 90 100

NI PKHNMKA FLDELKAENI KKFLYNFTQI PHLAGTEQNF QLAKQIQSQW

110 120 130 140 150

KEFGLDSVEL AHYDVLLSYP NKTHPNYISI INEDGNEIFN TSLFEPPPPG

160 170 180 190 200

YENVSDIVPP FSAFSPQGMP EGDLVYVNYA RTEDFFKLER DMKINCSGKI

210 220 230 240 250

VIARYGKVFR GNKVKNAQLA GAKGVILYSD PADYFAPGVK SYPDGWNLPG

260 270 280 290 300

GGVQRGNILN LNGAGDPLTP GYPANEYAYR RGIAEAVGLP SIPVHPIGYY

310 320 330 340 350

DAQKLLEKMG GSAPPDSSWR GSLKVPYNVG PGFTGNFSTQ KVKMHIHSTN

360 370 380 390 400

EVTRIYNVIG TLRGAVEPDR YVILGGHRDS WVFGGIDPQS GAAVVHEIVR

410 420 430 440 450

SFGTLKKEGW RPRRTILFAS WDAEEFGLLG STEWAEENSR LLQERGVAYI

460 470 480 490 500

NADSSIEGNY TLRVDCTPLM YSLVHNLTKE LKSPDEGFEG KSLYESWTKK

510 520 530 540 550

SPSPEFSGMP RISKLGSGND FEVFFQRLGI ASGRARYTKN WETNKFSGYP

560 570 580 590 600

LYHSVYETYE LVEKFYDPMF KYHLTVAQVR GGMVFELANS IVLPFDCRDY

610 620 630 640 650 AVVLRKYADK IYSISMKHPQ EMKTYSVSFD SLFSAVKNFT EIASKFSERL

660 670 680 690 700

QDFDKSNPIV LRMMNDQLMF LERAFIDPLG LPDRPFYRHV I YAPSSHNKY

710 720 730 740 750

AGESFPGI YD ALFDIESKVD PSKAWGEVKR QIYVAAFTVQ AAAETLSEVA

[0056] PAP (prostatic acid phosphatase) (accession no. PI 5309) is a non-specific tyrosine phosphatase that dephosphorylates a diverse number of substrates under acidic conditions (pH 4-6) including alkyl, aryl, and acyl orthophosphate monoesters and phosphorylated proteins. PAP has lipid phosphatase activity and inactivates lysophosphatidic acid in seminal plasma. In one embodiment, a described PAP polynucleotide comprises a sequence encoding at least one MHC class I epitope or at least one MHC class II epitope. Similarly, the PAP polypeptides described herein include at least one MHC class I epitope or at least one MHC class II epitope. The human canonical sequence of PAP (Swiss Prot entry P15309) is set forth as SEQIDNO:64:

10 20 30 40 50

MRAAPLLLAR AASLSLGFLF LLFFWLDRSV LAKELKFVTL VFRHGDRSPI

60 70 80 90 100

DTFPTDPIKE SSWPQGFGQL TQLGMEQHYE LGEYIRKRYR KFLNESYKHE

110 120 130 140 150

QVYIRSTDVD RTLMSAMTNL AALFPPEGVS IWNPILLWQP IPVHTVPLSE

160 170 180 190 200

DQLLYLPFRN CPRFQELESE TLKSEEFQKR LHPYKDFIAT LGKLSGLHGQ

210 220 230 240 250

DLFGIWSKVY DPLYCESVHN FTLPSWATED TMTKLRELSE LSLLSLYGIH

260 270 280 290 300

KQKEKSRLQG GVLVNE I LNH MKRATQIPSY KKLIMYSAHD TTVSGLQMAL

310 320 330 340 350

DVYNGLLPPY ASCHLTELYF EKGEYFVEMY YRNETQHEPY PLMLPGCSPS

360 370 380

CPLERFAELV GPVIPQDWST ECMTTNSHQG TEDSTD

[0057] The predictive algorithm "BIMAS" ranks potential HLA binding epitopes according to the predictive half-time disassociation of peptide/HLA complexes. The

"SYFPEITHI" algorithm ranks peptides according to a score that accounts for the presence of primary and secondary HLA-binding anchor residues. Both computerized algorithms score candidate epitopes based on amino acid sequences within a given protein that have similar binding motifs to previously published HLA binding epitopes. Other algorithms can also be used to identify candidates for further biological testing.

Table 3

[0058] EGFRvIII-SSX2 fusion proteins

[0059] Disclosed herein are fusion proteins comprising an epidermal growth factor receptor variant III (EGFRvIII) polypeptide and a synovial sarcoma, X breakpoint 2 (SSX2) polypeptide. [0060] The fusion protein can comprise one or more copies of an EGFRvIII polypeptide. In some embodiments, the fusion protein can comprise one EGFRvIII polypeptide. In other embodiments, the fusion protein can comprise a plurality of EGFRvIII polypeptides. Suitable numbers of copies of the EGFRvIII polypeptide include, but are not limited to, 2, 3, 4, 5, or more copies. In some embodiments, for example, the fusion protein can comprise one EGFRvIII polypeptide (referred to as EGFRvIIIxl). Thus, in some aspects, the fusion protein can comprise an EGFRvIIIxl -SSX2 fusion protein. In some embodiments, for example, the fusion protein can comprise two copies of the EGFRvIII polypeptide (referred to as

EGFRvIIIx2). Thus, in some aspects, the fusion protein can comprise an EGFRvIIIx2-SSX2 fusion protein. In some embodiments, for example, the fusion protein can comprise three copies of the EGFRvIII polypeptide (referred to as EGFRvIIIx3). Thus, in some aspects, the fusion protein can comprise an EGFRvIIIx3-SSX2 fusion protein. In some embodiments, for example, the fusion protein can comprise four copies of the EGFRvIII polypeptide (referred to as EGFRvIIIx4). Thus, in some aspects, the fusion protein can comprise an EGFRvIIIx4- SSX2 fusion protein. In some embodiments, for example, the fusion protein can comprise five copies of the EGFRvIII polypeptide (referred to as EGFRvIIIx5). Thus, in some aspects, the fusion protein can comprise an EGFRvIIIx5-SSX2 fusion protein.

[0061] Each of the one or more copies of the EGFRvIII polypeptide can comprise an amino acid sequence that is at least 90% identical, 91% identical, 92% identical, 93% identical, 94% identical, 95% identical, 96% identical, 97% identical, 98% identical, 99% identical, or 100% identical to SEQ ID NO:6. In some embodiments, for example, the EGFRvIII polypeptide can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6. In other embodiments, the EGFRvIII polypeptide can comprise 2, 3, 4, 5, or more copies of an EGFRvIII polypeptide, each copy having an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6. In some embodiments, the EGFRvIII polypeptide is SEQ ID NO:6. An exemplary amino acid sequence of

EGFRvIIIx5 is set forth in SEQ ID NO:8.

[0062] In some aspects, each of the one or more copies of the EGFRvIII polypeptide can consist of an amino acid sequence that is at least 90% identical, 91% identical, 92% identical, 93% identical, 94% identical, 95% identical, 96% identical, 97% identical, 98% identical, 99%) identical, or 100%> identical to SEQ ID NO:6. In some aspects, each of the one or more copies of the EGFRvIII polypeptide can consist essentially of an amino acid sequence that is at least 90% identical, 91% identical, 92% identical, 93% identical, 94% identical, 95% identical, 96% identical, 97% identical, 98% identical, 99% identical, or 100% identical to SEQ ID NO:6.

[0063] The one or more copies of EGFRvIII polypeptide can comprise, consist, of, or consist essentially of an amino acid sequence at least 90% identical to amino acid residues 6 to 18 of SEQ ID NO:6. In some embodiments, the one or more copies of EGFRvIII polypeptide can comprise, consist, of, or consist essentially of an amino acid sequence at least 90% identical to amino acid residues 6 to 14 of SEQ ID NO:6.

[0064] The EGFRvIII polypeptides can be flanked by one or more cleaver sequences at the N-terminus, C-terminus, or both the N- and C-terminus of the EGFRvIII polypeptide. Cleaver sequences are configured to be processed by proteases present in the subject. Where the EGFRvIII polypeptide comprises 2 or more copies of the EGFRvIII polypeptide, cleaver sequences can be present between the individual copies of the EGFRvIII polypeptides. For example, and without intending to be limiting, SEQ ID NO: 8 contains 5 copies of the EGFRvIII polypeptide (each copy of the EGFRvIII polypeptide set forth in SEQ ID NO:6) and cleaver sequences (ASKVL/ADGSVKTS (SEQ ID NO:54), ASKVA/GDGSIK (SEQ ID NO:55), LSKVL/ADGSVK (SEQ ID NO:56), ASKVA/GDGSIK (SEQ ID NO:57), and LSKVL/ADGSVK (SEQ ID NO:58); wherein "/" represents an EGFRvIII polypeptide). These cleaver sequences are exemplary in nature only. Suitable cleaver sequences are described in U.S. Patent App. No. 13/988,076 (U.S. Patent Publ. No. 2014/037662); Toes, et al., J. Exp. Med. (2001) 194: 1-12; Lauer et al., Infect. Immun. (2008) 76: 3742-53; and Sinnathamby et al., J. Immunother. (2009) 32: 856-69, each of which are incorporated by reference in its entirety.

[0065] The EGFRvIII polypeptide can be fused to the N-terminus or C-terminus of the SSX2 polypeptide. Preferably, the EGFRvIII polypeptide can be fused to the N-terminus of the SSX2 polypeptide.

[0066] Suitable SSX2 polypeptides include amino acids 1-234 of SSX2 ("SSX2" or "SSX2i _-2 3 ₄ ") and amino acids 2-234 of SSX2 ("SSX2 _2-2 3 ₄ "). In some embodiments, the SSX2 polypeptide can comprise, consist of, or consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10. In some aspects, the SSX2 polypeptide is SEQ ID NO: 10. In some embodiments, the SSX2 polypeptide can comprise, consist of, or consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 _2-2 34 as set forth in amino acid residues 2-234 of SEQ ID NO: 10.

[0067] The fusion protein can comprise one or more EGFRvIII polypeptides, wherein the EGFRvIII polypeptides comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10. In some

embodiments, the fusion protein can comprise one or more EGFRvIII polypeptides, wherein the EGFRvIII polypeptides comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 _2-234 as set forth in amino acid residues 2-234 of SEQ ID NO: 10.

[0068] The fusion protein can comprise an amino acid sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth as amino acid residues 89 to 475 of SEQ ID NO:4.

[0069] The disclosed fusion proteins can further comprise a signal sequence, wherein the signal sequence is in translational reading frame with the EGFRvIII polypeptide and the SSX2 polypeptide. Suitable signal sequences include, for example, ActANlOO (as set forth in SEQ ID NO:60), ActANlOO* (as set forth in SEQ ID NO:2), LL0441 (as set forth in SEQ ID NO:49), LL0441APEST (as set forth in SEQ ID NO:51), and ΙΧ0441Δ26 (as set forth in SEQ ID NO:53). In some embodiments, the signal sequence can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO as set forth in SEQ ID NO:60. In some embodiments, the signal sequence can comprise an amino acid sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2. Accordingly, in some embodiments, the fusion protein can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO*- EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:4.

[0070] The disclosed fusion proteins can be expressed in a number of suitable host cells as disclosed elsewhere herein. In some embodiments, for example, the fusion protein can be expressed in a bacterium, such as Listeria monocytogenes or a genetically modified form thereof. [0071] Also disclosed are nucleic acid molecules encoding an EGFRvIII-SSX2 fusion protein. The disclosed nucleic acid molecules can encode any of the EGFRvIII-SSX2 fusion proteins disclosed herein.

[0072] The nucleic acid molecules can encode an EGFRvIII-SSX2 fusion protein with one or more EGFRvIII polypeptides. In some embodiments, the nucleic acid molecule can encode an EGFRvIII-SSX2 fusion protein with one EGFRvIII polypeptide. In other embodiments, the nucleic acid molecule can encode an EGFRvIII-SSX2 fusion protein with a plurality of EGFRvIII polypeptides. Suitable numbers of EGFRvIII polypeptides encoded by the disclosed nucleic acid molecules include, but are not limited to, 2, 3, 4, 5, or more copies. In some embodiments, the nucleic acid molecules can encode an EGFRvIII-SSX2 fusion protein with 5 copies of the EGFRvIII polypeptide (EGFRvIIIx5). Each EGFRvIII polypeptide can be encoded by an EGFRvIII polynucleotide having a nucleotide sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:5. An exemplary nucleic acid sequence of an EGFRvIIIx5 polynucleotide is set forth in SEQ ID NO:7. Accordingly, the disclosed nucleic acid molecules can encode an EGFRvIII- SSX2 fusion protein comprising one or more EGFRvIII polypeptides, wherein the EGFRvIII polypeptides are encoded by a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5. In some aspects, the nucleic acid molecule is operably linked to a promoter. For example, the nucleic acid molecules can encode an EGFRvIII-SSX2 fusion protein, wherein the EGFRvIII polypeptide is encoded by a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIIIx5 polynucleotide as set forth in SEQ ID NO:7. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[0073] The disclosed nucleic acid molecules can encode an EGFRvIII-SSX2 fusion protein, wherein the SSX2 polypeptide is encoded by a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the SSX2

polynucleotide as set forth in SEQ ID NO:9. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[0074] In some embodiments, the nucleic acid molecule can comprise one or more polynucleotides that are at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO: 5 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the SSX2 polynucleotide as set forth in SEQ ID NO:9. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[0075] The nucleic acid molecule can encode an EGFRvIIIx5-SSX2 fusion protein. In some embodiments, the nucleic acid molecule can comprise a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIIIx5 polynucleotide as set forth in SEQ ID NO:7 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the SSX2

polynucleotide as set forth in SEQ ID NO:9. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[0076] The nucleic acid molecule can further comprise a promoter, a signal sequence, or both, wherein the promoter, signal sequence, or both are operably linked with the nucleotide sequence encoding the EGFRvIII polypeptide and the nucleotide sequence encoding the SSX2 polypeptide. Suitable promoters include, for example, actA (as set forth in SEQ ID NO:21) or ly (as set forth in SEQ ID NO:47). The promoter can comprise, for example, a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to an actA promoter as set forth in SEQ ID NO:21. Suitable signal sequences include, for example, ActANlOO (as set forth in SEQ ID NO:59), ActANlOO* (as set forth in SEQ ID NO: 1), LL0441 (as set forth in SEQ ID NO:48), LL0441APEST (as set forth in SEQ ID NO:50), and LL0441A26 (as set forth in SEQ ID NO:52). The signal sequence can comprise, for example, a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth in SEQ ID NO: l . Accordingly, in some embodiments, the nucleic acid molecule encoding the

EGFRvIII-SSX2 fusion protein can comprise, consist of, or consist essentially of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to cictA-ActAN100*-EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3.

[0077] The nucleic acid molecules can further comprise additional nucleic acid sequences including, but not limited to, restriction endonuclease cleavage sites (cloning linkers). The nucleic acid molecules can be generated using a number of suitable restriction endonucleases, wherein the endonuclease cleavage site(s) may remain in the final nucleic acid molecule.

[0078] Additional nucleic acid sequences that can be included in the nucleic acid molecules include "cleaver sequences" (as defined elsewhere herein) which flank the individual EGFRvIII polynucleotides. [0079] The nucleic acid molecule can be part of an expression cassette. The expression cassette can comprise a promoter, an open reading frame comprising the disclosed nucleic acid molecules, and a 3' untranslated region. The expression cassette can be used to direct a host cell's machinery to produce the disclosed fusion proteins.

[0080] Vectors comprising the disclosed nucleic acid molecules are also provided.

Suitable vectors include, for example, bacterial vectors, viral vectors, naked DNA vectors, and naked RNA vectors.

[0081] EGFRvIII- PAP fusion proteins

[0082] Disclosed herein are fusion proteins comprising an EGFRvIII polypeptide and a prostatic acid phosphatase (PAP) polypeptide.

[0083] The fusion protein can comprise one or more copies of an EGFRvIII polypeptide. In some embodiments, the fusion protein can comprise one EGFRvIII polypeptide. In other embodiments, the fusion protein can comprise a plurality of EGFRvIII polypeptides. Suitable numbers of copies of the EGFRvIII polypeptide include, but are not limited to, 2, 3, 4, 5, or more copies. In some embodiments, for example, the fusion protein can comprise one EGFRvIII polypeptide (referred to as EGFRvIIIxl). Thus, in some aspects, the fusion protein can comprise an EGFRvIIIxl -PAP fusion protein. In some embodiments, for example, the fusion protein can comprise two copies of the EGFRvIII polypeptide (referred to as

EGFRvIIIx2). Thus, in some aspects, the fusion protein can comprise an EGFRvIIIx2-PAP fusion protein. In some embodiments, for example, the fusion protein can comprise three copies of the EGFRvIII polypeptide (referred to as EGFRvIIIx3). Thus, in some aspects, the fusion protein can comprise an EGFRvIIIx3-PAP fusion protein. In some embodiments, for example, the fusion protein can comprise four copies of the EGFRvIII polypeptide (referred to as EGFRvIIIx4). Thus, in some aspects, the fusion protein can comprise an EGFRvIIIx4- PAP fusion protein. In some embodiments, for example, the fusion protein can comprise five copies of the EGFRvIII polypeptide (referred to as EGFRvIIIx5). Thus, in some aspects, the fusion protein can comprise an EGFRvIIIx5-PAP fusion protein.

[0084] Each of the one or more copies of the EGFRvIII polypeptide can comprise an amino acid sequence that is at least 90% identical, 91% identical, 92% identical, 93% identical, 94% identical, 95% identical, 96% identical, 97% identical, 98% identical, 99% identical, or 100% identical to SEQ ID NO:6. In some embodiments, for example, the EGFRvIII polypeptide can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6. In other embodiments, the EGFRvIII polypeptide can comprise 2, 3, 4, 5, or more copies of an EGFRvIII polypeptide, each copy having an amino acid sequence at least 90% identical to SEQ ID NO:6. An exemplary amino acid sequence of EGFRvIIIx5 is set forth in SEQ ID NO:8.

[0085] In some aspects, each of the one or more copies of the EGFRvIII polypeptide can consist of an amino acid sequence that is at least 90% identical, 91% identical, 92% identical, 93% identical, 94% identical, 95% identical, 96% identical, 97% identical, 98% identical, 99% identical, or 100% identical to SEQ ID NO:6. In some aspects, each of the one or more copies of the EGFRvIII polypeptide can consist essentially of an amino acid sequence that is at least 90% identical, 91% identical, 92% identical, 93% identical, 94% identical, 95% identical, 96% identical, 97% identical, 98% identical, 99% identical, or 100% identical to SEQ ID NO:6.

[0086] In some embodiments, the one or more copies of EGFRvIII polypeptide can comprise, consist, of, or consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to amino acid residues 6 to 18 of SEQ ID NO:6. In some embodiments, the one or more copies of EGFRvIII polypeptide can comprise, consist, of, or consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to amino acid residues 6 to 14 of SEQ ID NO:6.

[0087] The EGFRvIII polypeptides can be flanked by one or more cleaver sequences at the N-terminus, C-terminus, or both the N- and C-terminus of the EGFRvIII polypeptide. Cleaver sequences are configured to be processed by proteases present in the subject. Where the EGFRvIII polypeptide comprises 2 or more copies of the EGFRvIII polypeptide, cleaver sequences can be present between the individual copies of the EGFRvIII polypeptides. For example, and without intending to be limiting, SEQ ID NO: 8 contains 5 copies of the EGFRvIII polypeptide (each copy of the EGFRvIII polypeptide set forth in SEQ ID NO:6) and cleaver sequences (ASKVL/ADGSVKTS (SEQ ID NO:54), ASKVA/GDGSIK (SEQ ID NO:55), LSKVL/ADGSVK (SEQ ID NO:56), ASKVA/GDGSIK (SEQ ID NO:57), and LSKVL/ADGSVK (SEQ ID NO:58); wherein "/" represents an EGFRvIII polypeptide). These cleaver sequences are exemplary in nature only. Suitable cleaver sequences are described in U.S. Patent App. No. 13/988,076 (U.S. Patent Publ. No. 2014/037662); Toes, et al., J. Exp. Med. (2001) 194: 1-12; Lauer et al., Infect. Immun. (2008) 76: 3742-53; and Sinnathamby et al., J. Immunother. (2009) 32: 856-69, each of which are incorporated by reference in its entirety. [0088] The EGFRvIII polypeptide can be fused to the N-terminus or C-terminus of the PAP polypeptide. Preferably, EGFRvIII polypeptide can be fused to the N-terminus of the PAP polypeptide

[0089] Suitable PAP polypeptides include amino acids 33-386 of PAP ("ΡΑΡ33-386")· Thus, in some embodiments, the PAP polypeptide can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14. In some embodiments, the PAP polypeptide can consist of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14. In some embodiments, the PAP polypeptide can consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14.

[0090] In some embodiments, the fusion protein can comprise a polypeptide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polypeptide as set forth in SEQ ID NO:6 and a polypeptide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%. identical to the PAP _33-386 polypeptide as set forth in SEQ ID NO: 14. For example, the fusion protein can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIxl-PAP33.3 ₈ 6 as set forth in amino acid residues 89 to 476 of SEQ ID NO:35. In some embodiments, the fusion protein can comprise two polypeptides that are at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polypeptide as set forth in SEQ ID NO: 6 and a polypeptide at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%. identical to the PAP33 _-38 6 polypeptide as set forth in SEQ ID NO: 14. For example, the fusion protein can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx2-PAP ₃ 3-3 ₈ 6 as set forth in amino acid residues 89 to 509 of SEQ ID NO:37. In some embodiments, the fusion protein can comprise three polypeptides that are at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polypeptide as set forth in SEQ ID NO:6 and a polypeptide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%. identical to the PAP33 _-38 6 polypeptide as set forth in SEQ ID NO: 14. For example, the fusion protein can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%. identical to EGFRvIIIx3-PAP ₃₃ .3 ₈₆ as set forth in amino acid residues 89 to 541 of SEQ ID NO:39. In some embodiments, the fusion protein can comprise four polypeptides that are at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polypeptide as set forth in SEQ ID NO:6 and a polypeptide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%. identical to the PAP ₃ 3 _-386 polypeptide as set forth in SEQ ID NO: 14. For example, the fusion protein can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx4-PAP _33-386 as set forth in amino acid residues 89 to 573 of SEQ ID NO:41. In some embodiments, the fusion protein can comprise five polypeptides that are at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polypeptide as set forth in SEQ ID NO: 6 and a polypeptide at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%. identical to the PAP _33-386 polypeptide as set forth in SEQ ID NO: 14. For example, the fusion protein can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx5-PAP _33-386 as set forth in amino acid residues 89 to 606 of SEQ ID NO: 12.

[0091] The disclosed fusion proteins further comprise a signal sequence, wherein the signal sequence is in translational reading frame with the EGFRvIII polypeptide and the PAP polypeptide. Suitable signal sequences include, for example, ActANlOO (as set forth in SEQ ID NO:60), ActANlOO* (as set forth in SEQ ID NO:2), LL0441 (as set forth in SEQ ID NO:49), LL0441APEST (as set forth in SEQ ID NO:51), and ΙΧ0441Δ26 (as set forth in SEQ ID NO:53). In some embodiments, the signal sequence can comprise an amino acid sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2. In some embodiments, the signal sequence can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO as set forth in SEQ ID NO:60.

Accordingly, in some embodiments, the fusion protein can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-EGFRvIIIxl-PAP _33-386 as set forth in SEQ ID NO:35. In some embodiments, the fusion protein can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-EGFRvIIIx2-PAP _33-386 as set forth in SEQ ID NO:37. In some embodiments, the fusion protein can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-EGFRvIIIx3-PAP _33-386 as set forth in SEQ ID NO:39. In some embodiments, the fusion protein can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO*- EGFRvIIIx4-PAP33.386 as set forth in SEQ ID NO:41. In some embodiments, the fusion protein can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-EGFRvIIIx5-PAP ₃ 3-386 as set forth in SEQ ID NO: 12.

[0092] The disclosed fusion proteins can be expressed in a number of suitable host cells as disclosed elsewhere herein. In some embodiments, for example, the fusion protein can be expressed in a bacterium, such as Listeria monocytogenes or a genetically modified form thereof.

[0093] Also disclosed are nucleic acid molecules encoding an EGFRvIII-PAP fusion protein. The disclosed nucleic acid molecules can encode any of the EGFRvIII-PAP fusion proteins disclosed herein.

[0094] The nucleic acid molecules can encode an EGFRvIII-PAP fusion protein with one or more EGFRvIII polypeptides. In some embodiments, the nucleic acid molecule can encode an EGFRvIII-PAP fusion protein with one EGFRvIII polypeptide. In other embodiments, the nucleic acid molecule can encode an EGFRvIII-PAP fusion protein with a plurality of EGFRvIII polypeptides. Suitable numbers of EGFRvIII polypeptides encoded by the disclosed nucleic acid molecules include, but are not limited to, 2, 3, 4, 5, or more copies. In some embodiments, the nucleic acid molecules can encode an EGFRvIII-PAP fusion protein with 1 copy of the EGFRvIII polypeptide (EGFRvIIIxl), 2 copies of the EGFRvIII polypeptide (EGFRvIIIx2), 3 copies of the EGFRvIII polypeptide (EGFRvIIIx3), 4 copies of the EGFRvIII polypeptide (EGFRvIIIx4), or 5 copies of the EGFRvIII polypeptide

(EGFRvIIIx5). An exemplary nucleic acid sequence of an EGFRvIII polynucleotide is set forth in SEQ ID NO: 5 and an exemplary nucleic acid sequence of an EGFRvIIIx5

polynucleotide is set forth in SEQ ID NO:7. Accordingly, the disclosed nucleic acid molecules can encode an EGFRvIII-PAP fusion protein, wherein the fusion protein comprises 1, 2, 3, 4, or 5 copies of an EGFRvIII polypeptide encoded by a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some aspects, the disclosed nucleic acid molecules can encode an EGFRvIII-PAP fusion protein, wherein the EGFRvIII polypeptide is encoded by a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIIIx5 polynucleotide as set forth in SEQ ID NO:7. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[0095] The disclosed nucleic acid molecules can encode an EGFRvIII-PAP fusion protein, wherein the PAP polypeptide is encoded by a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the PAP 33-386 polynucleotide as set forth in SEQ ID NO: 13. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[0096] In some embodiments, the nucleic acid molecule can comprise one or more EGFRvIII polynucleotides, wherein each EGFRvIII polynucleotide is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the PAP ₃ 3_ ₃₈₆ polynucleotide as set forth in SEQ ID NO: 13. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the nucleic acid molecule can comprise a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIIIx5 polynucleotide as set forth in SEQ ID NO:7 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to the PAP 33.386 polynucleotide as set forth in SEQ ID NO: 13. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[0097] The nucleic acid molecule can further comprise a promoter, a signal sequence, or both, wherein the promoter, signal sequence, or both are operably linked with the nucleotide sequence encoding the EGFRvIII polypeptide and the nucleotide sequence encoding the PAP polypeptide. Suitable promoters include, for example, actA (as set forth in SEQ ID NO:21) or hly (as set forth in SEQ ID NO:47). The promoter can comprise, for example, a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to an actA promoter as set forth in SEQ ID NO:21. Suitable signal sequences include, for example, ActANlOO (as set forth in SEQ ID NO:59), ActANlOO* (as set forth in SEQ ID NO: 1), LL0441 (as set forth in SEQ ID NO:48), LL0441APEST (as set forth in SEQ ID NO:50), and LL0441A26 (as set forth in SEQ ID NO:52). The signal sequence can comprise, for example, a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth in SEQ ID NO: l . Accordingly, in some embodiments, the nucleic acid molecule encoding the

EGFRvIII-PAP fusion protein can comprise, consist of, or consist essentially of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to actA-ActAN100*-EGFRvIIIxl-PAP ₃₃ -386 as set forth in SEQ ID NO:34. In some embodiments, the nucleic acid molecule encoding the EGFRvIII-PAP fusion protein can comprise, consist of, or consist essentially of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to actA-ActANlOO*- EGFRvIIIx2-PAP 33-386 as set forth in SEQ ID NO:36. In some embodiments, the nucleic acid molecule encoding the EGFRvIII-PAP fusion protein can comprise, consist of, or consist essentially of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to actA-ActAN 100* -EGFRvIIIx3-PAP 33-386 as set forth in SEQ ID NO:38. In some embodiments, the nucleic acid molecule encoding the EGFRvIII-PAP fusion protein can comprise, consist of, or consist essentially of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to actA- ActAN100*-EGFRvIIIx4-PAP 33-386 as set forth in SEQ ID NO:40. In some embodiments, the nucleic acid molecule encoding the EGFRvIII-PAP fusion protein can comprise, consist of, or consist essentially of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to actA-ActAN 100*-EGFRvIIIx5-PAP 33.386 as set forth in SEQ ID NO: 11.

[0098] The nucleic acid molecules can further comprise additional nucleic acid sequences including, but not limited to, restriction endonuclease cleavage sites (cloning linkers) and "cleaver sequences" (as defined elsewhere herein).

[0099] The nucleic acid molecule can be part of an expression cassette. The expression cassette can comprise a promoter, an open reading frame comprising the disclosed nucleic acid molecules, and a 3' untranslated region. The expression cassette can be used to direct a host cell's machinery to produce the disclosed fusion proteins.

[00100] Vectors comprising the disclosed nucleic acid molecules are also provided.

Suitable vectors include, for example, bacterial vectors, viral vectors, naked DNA vectors, and naked RNA vectors.

[00101] EGFRvIII-NKX3.1-PSMA fusion proteins

[00102] Disclosed herein are fusion proteins comprising an EGFRvIII polypeptide, an NK3 homeobox 1 (NKX3.1) polypeptide, and a prostate-specific membrane antigen (PSMA) polypeptide.

[00103] The fusion protein can comprise one or more copies of an EGFRvIII polypeptide. In some embodiments, the fusion protein can comprise one EGFRvIII polypeptide. In other embodiments, the fusion protein can comprise a plurality of EGFRvIII polypeptides. Suitable numbers of copies of the EGFRvIII polypeptide include, but are not limited to, 2, 3, 4, 5, or more copies. In some embodiments, for example, the fusion protein can comprise one EGFRvIII polypeptide (referred to as EGFRvIIIxl). In some embodiments, for example, the fusion protein can comprise two copies of the EGFRvIII polypeptide (referred to as

EGFRvIIIx2). In some embodiments, for example, the fusion protein can comprise three copies of the EGFRvIII polypeptide (referred to as EGFRvIIIx3). In some embodiments, for example, the fusion protein can comprise four copies of the EGFRvIII polypeptide (referred to as EGFRvIIIx4). In some embodiments, for example, the fusion protein can comprise five copies of the EGFRvIII polypeptide (referred to as EGFRvIIIx5).

[00104] Each of the one or more copies of the EGFRvIII polypeptide can comprise an amino acid sequence that is at least 90% identical, 91% identical, 92% identical, 93% identical, 94% identical, 95% identical, 96% identical, 97% identical, 98% identical, 99% identical, or 100% identical to SEQ ID NO:6. In some embodiments, for example, the EGFRvIII polypeptide can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6. In other embodiments, the EGFRvIII polypeptide can comprise 2, 3, 4, 5, or more copies of an EGFRvIII polypeptide, each copy having an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to SEQ ID NO:6. An exemplary amino acid sequence of EGFRvIIIx5 is set forth in SEQ ID NO:8.

[00105] In some aspects, each of the one or more copies of the EGFRvIII polypeptide can consist of an amino acid sequence that is at least 90% identical, 91% identical, 92% identical, 93% identical, 94% identical, 95% identical, 96% identical, 97% identical, 98% identical, 99%) identical, or 100%> identical to SEQ ID NO:6. In some aspects, each of the one or more copies of the EGFRvIII polypeptide can consist essentially of an amino acid sequence that is at least 90% identical, 91% identical, 92% identical, 93% identical, 94% identical, 95% identical, 96% identical, 97% identical, 98% identical, 99% identical, or 100% identical to SEQ ID NO:6.

[00106] In some embodiments, the one or more copies of EGFRvIII polypeptide can comprise, consist, of, or consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to amino acid residues 6 to 18 of SEQ ID NO:6. In some embodiments, the one or more copies of EGFRvIII polypeptide can comprise, consist, of, or consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to amino acid residues 6 to 14 of SEQ ID NO:6.

[00107] The EGFRvIII polypeptides can be flanked by one or more cleaver sequences at the N-terminus, C-terminus, or both the N- and C-terminus of the EGFRvIII polypeptide. Cleaver sequences are configured to be processed by proteases present in the subject. Where the EGFRvIII polypeptide comprises 2 or more copies of the EGFRvIII polypeptide, cleaver sequences can be present between the individual copies of the EGFRvIII polypeptides. For example, and without intending to be limiting, SEQ ID NO: 8 contains 5 copies of the EGFRvIII polypeptide (each copy of the EGFRvIII polypeptide set forth in SEQ ID NO:6) and cleaver sequences (ASKVL/ADGSVKTS (SEQ ID NO:54), ASKVA/GDGSIK (SEQ ID NO:55), LSKVL/ADGSVK (SEQ ID NO:56), ASKVA/GDGSIK (SEQ ID NO:57), and LSKVL/ADGSVK (SEQ ID NO:58); wherein "/" represents an EGFRvIII polypeptide). These cleaver sequences are exemplary in nature only. Suitable cleaver sequences are described in U.S. Patent App. No. 13/988,076 (U.S. Patent Publ. No. 2014/037662); Toes, et al., J. Exp. Med. (2001) 194: 1-12; Lauer et al., Infect. Immun. (2008) 76: 3742-53; and Sinnathamby et al., J. Immunother. (2009) 32: 856-69, each of which are incorporated by reference in its entirety.

[00108] Preferably, the fusion protein can comprise an EGFRvIII polypeptide fused to the N-terminus of the NKX3.1 polypeptide, and an NKX3.1 polypeptide fused to the N-terminus of the PSMA polypeptide. Other orders of the EGFRvIII polypeptide, NKX3.1 polypeptide, and PSMA polypeptide are also suitable. For example: EGFRvIII-PSMA-NKXl; PSMA- NKX- EGFRvIII; PSMA-EGFRvIII-NKXl; NKXl-EGFRvIII-PSMA; and NKXl-PSMA- EGFRvIII fusion proteins are suitable.

[00109] Suitable NKX3.1 polypeptides include amino acids 11-234 of NKX3.1

("NKX3.111-234")· In some embodiments, the NKX3.1 polypeptide can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to KX3.1 n. ₂₃ 4 as set forth in SEQ ID NO:25. In some embodiments, the NKX3.1 polypeptide can consist of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 ii _-23 4 as set forth in SEQ ID NO:25. In some embodiments, the NKX3.1 polypeptide can consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.111.234 as set forth in SEQ ID NO:25. [00110] The KX3.111-234 polypeptide can have an arginine (R) to glycine (G) mutation at amino acid 41 (" KX3.1(R41G)"). In some embodiments, the NKX3.1 polypeptide can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to KX3.1(R41G)n _-2 34 as set forth in SEQ ID NO: 18. In some embodiments, the KX3.1 polypeptide can consist of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

KX3.1(R41G)ii _-2 34 as set forth in SEQ ID NO: 18. In some embodiment, the NKX3.1 polypeptide can consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3. l(R41G)n _-2 34 as set forth in SEQ ID NO: 18.

[00111] Suitable PSMA polypeptides include amino acids 1-20 and 44-750 of PSMA (PSMAi _-20; 44-75o) or amino acids 1-20, 44-138, and 169-750 of PSMA ("PSMAi _{-20; 4} 4-i38, 169- 75ο")· Preferrably, the PSMA polypeptide can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi -20, 44-138, 169-750 as set forth in SEQ ID NO:20. In some embodiments, the PSMA polypeptide can consist of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%. identical to PSMAi _-20 , ₄₄ . ₁₃₈ , 169-750 as set forth in SEQ ID NO:20. In some embodiments, the PSMA polypeptide can consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20; 44-138, 169-750 as set forth in SEQ ID NO:20.

[00112] EGFRvIII-NKX3.1 ii _-2 34-PSMAi _-2 o, 44-138, 169-750 fusion proteins can comprise: a) one or more EGFRvIII polypeptides having an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 ιι _-234 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _{-20; 44} . _{138; 16} 9- 750 as set forth in SEQ ID NO:20;

b) an EGFRvIIIx5 polypeptide having an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:8, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to KX3.111.234 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-2 o, 44-138, 169-750 as set forth in SEQ ID NO:20; or

c) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1 ii-234-PSMAi _-2 o, 44-i38, 169-750 as set forth in amino acid residues 89 to 1177 of SEQ ID NO:23.

[00113] EGFRvIIIx5- KX3.1(R41G)ii _-2 34-PSMAi _{-20; 4} 4-i38, 169-750 fusion proteins can comprise:

a) one or more EGFRvIII polypeptides having an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6, a KX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to KX3.1(R41G)ii _-234 as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _{-20, 44} . _{138; 16} 9- 750 as set forth in SEQ ID NO:20;

b) an EGFRvIIIx5 polypeptide having an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:8, a KX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to KX3. l(R41G)ii-234 as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99%) identical, or iv) 100%) identical to PSMAi _-2 o, 44-i3 ₈ , 169-750 as set forth in SEQ ID NO:20; or

c) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G)ii _-2 34-PSMAi. 20, 44-138, 169-750 as set forth in in amino acid residues 89 to 1177 of SEQ ID NO: 16.

[00114] The disclosed fusion proteins can further comprise a signal sequence. In some embodiments, the fusion protein can further comprise a signal sequence, wherein the signal sequence is in translational reading frame with the EGFRvIII polypeptide, NKX3.1 polypeptide, and the PSMA polypeptide. Suitable signal sequences include, for example, ActANlOO (as set forth in SEQ ID NO:60), ActANlOO* (as set forth in SEQ ID NO:2), LL0441 (as set forth in SEQ ID NO:49), LL0441APEST (as set forth in SEQ ID NO:51), and ΙΧ0441Δ26 (as set forth in SEQ ID NO:53). In some embodiments, the signal sequence can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO as set forth in SEQ ID NO:60. In some embodiments, the signal sequence can comprise an amino acid sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2. Accordingly, in some embodiments, the EGFRvIII-NKX3. l n.234- PSMAi-20, 44-138, 169-750 fusion proteins can comprise, consist of, or consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-EGFRvIIIx5-NKX3.1 ii-234-PSMAi _-2 o, 44-i38, 169-750 as set forth in SEQ ID NO:23. In some embodiments, the EGFRvIII-NKX3.1(R41G)ii-234-PSMAi _-2 o, 44- 138, 169-750 fusion proteins can comprise, consist of, or consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-EGFRvIIIx5-NKX3.1(R41G)n-234-PSMAi-2o, 44-138, 169-750 as set forth in SEQ ID NO: 16.

[00115] The disclosed fusion proteins can be expressed in a number of suitable host cells as disclosed elsewhere herein. In some embodiments, for example, the fusion protein can be expressed in a bacterium, such as Listeria monocytogenes or a genetically modified form thereof.

[00116] Also disclosed are nucleic acid molecules encoding a EGFRvIII-NKX3.1-PSMA fusion proteins. The disclosed nucleic acid molecules can encode any of the EGFRvIII- NKX3.1-PSMA fusion proteins disclosed herein.

[00117] The nucleic acid molecules can encode a EGFRvIII-NKX3.1-PSMA fusion protein with one or more EGFRvIII polypeptides. In some embodiments, the nucleic acid molecule can encode a EGFRvIII-NKX3.1-PSMA fusion protein with one EGFRvIII polypeptide. In other embodiments, the nucleic acid molecule can encode a EGFRvIII- NKX3.1-PSMA fusion protein with a plurality of EGFRvIII polypeptides. Suitable numbers of EGFRvIII polypeptides encoded by the disclosed nucleic acid molecules include, but are not limited to, 2, 3, 4, 5, or more copies. In some embodiments, the nucleic acid molecules can encode a EGFRvIII-NKX3.1-PSMA fusion protein with 5 copies of the EGFRvIII polypeptide (EGFRvIIIx5). An exemplary nucleic acid sequence of an EGFRvIII polynucleotide is set forth in SEQ ID NO:5 and an exemplary nucleic acid sequence of an EGFRvIIIx5 polynucleotide is set forth in SEQ ID NO:7. Accordingly, the disclosed nucleic acid molecules can encode a EGFRvIII-NKX3.1-PSMA fusion protein, wherein fusion protein comprises a plurality of EGFRvIII polypeptides each encoded by a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%> identical to the EGFRvIIIx5 polynucleotide as set forth in SEQ ID NO: 5. In some aspects, the nucleic acid molecule is operably linked to a promoter. The disclosed nucleic acid molecules can encode a EGFRvIII-NKX3.1-PSMA fusion protein, wherein the EGFRvIII polypeptide is encoded by a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to the EGFRvIIIx5 polynucleotide as set forth in SEQ ID NO:7. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00118] The disclosed nucleic acid molecules can encode a EGFRvIII-NKX3.1-PSMA fusion protein, wherein the NKX3.1 polypeptide is encoded by a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3.1 n-234 polynucleotide as set forth in SEQ ID NO:24. In some aspects, the nucleic acid molecule is operably linked to a promoter. Alternatively, the disclosed nucleic acid molecules can encode a EGFRvIII-NKX3.1-PSMA fusion protein, wherein the NKX3.1 polypeptide is encoded by a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3.1(R41G) n-234 polynucleotide as set forth in SEQ ID NO: 17. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00119] The disclosed nucleic acid molecules can encode a EGFRvIII-NKX3.1-PSMA fusion protein, wherein the PSMA polypeptide is encoded by a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the PSMA^o _, 44-138 _, 169-750 as set forth in SEQ ID NO: 19. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00120] The nucleic acid molecule encoding the EGFRvIII-NKX3.111.234-PSMA1.20, 44-138, 169-750 fusion proteins can comprise, consist of, or consist essentially of:

a) one or more EGFRvIII polynucleotides that are at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5, a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3. ln.234 polynucleotide as set forth in SEQ ID NO:24, and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the PSMA 1.20, 44-138, 109-750 as set forth in SEQ ID NO: 19; or

b) a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%> identical to the EGFRvIIIx5 polynucleotide as set forth in SEQ ID NO:7, a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3. I _n . ₂₃₄ polynucleotide as set forth in SEQ ID NO:24, and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the PSMA i. ₂₀ , 44-138, 109-750 as set forth in SEQ ID NO: 19.

[00121] In some aspects, the nucleic acid molecules listed above are operably linked to a promoter.

[00122] The nucleic acid molecule encoding the EGFRvIII-NKX3. l(R41G)n. ₂₃ 4-PSMAi. 20, 44-138, 169-750 fusion proteins can comprise, consist of, or consist essentially of:

a) one or more EGFRvIII polynucleotides that are at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5, a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3.1(R41G)n-234 polynucleotide as set forth in SEQ ID NO: 17, and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to the PSMA ]. ₂ o, 44-138, 109-750 as set forth in SEQ ID NO: 19; or

b) a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIIIx5 polynucleotide as set forth in SEQ ID NO:7, a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3.1(R41G) _n . ₂ 34 polynucleotide as set forth in SEQ ID NO: 17, and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the PSMA ]. ₂ o, 44-138, 109-750 as set forth in SEQ ID NO: 19.

[00123] In some aspects, the nucleic acid molecules listed above are operably linked to a promoter.

[00124] The nucleic acid molecule can further comprise a promoter, a signal sequence, or both, wherein the promoter, signal sequence, or both are operably linked with the nucleotide sequence encoding the EGFRvIII polypeptide, the NKX3.1 polypeptide, and the PSMA polypeptide. Suitable promoters include, for example, actA (as set forth in SEQ ID NO:21) or ly (as set forth in SEQ ID NO:47). The promoter can comprise, for example, a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to an actA promoter as set forth in SEQ ID NO:21. Suitable signal sequences include, for example, ActANlOO (as set forth in SEQ ID NO:59), ActANlOO* (as set forth in SEQ ID NO: 1), LL0441 (as set forth in SEQ ID NO:48), LL0441APEST (as set forth in SEQ ID NO:50), and LL0441A26 (as set forth in SEQ ID NO:52). The signal sequence can comprise, for example, a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth in SEQ ID NO: 1. Accordingly, in some embodiments, the nucleic acid molecule encoding the

EGFRvIII-NKX3.1-PSMA fusion protein can comprise, consist of, or consist essentially of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to actA-ActAN100*-EGFRvlllx5-NKX3.1 ₁₁ .234-PSMA ₁ . ₂ o, 44-iss, m-iso as set forth as SEQ ID NO:22. In other embodiments, the nucleic acid molecule encoding the EGFRvIII-NKX3.1-PSMA fusion protein can comprise, consist of, or consist essentially of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to actA-ActAN100*-EGFRvIIIx5-NKX3.1(R41G) ₁₁ .234-PSMA ₁ . ₂ o, 44-m. m-iso as set forth as SEQ ID NO: 15.

[00125] The nucleic acid molecules can further comprise additional nucleic acid sequences including, but not limited to, restriction endonuclease cleavage sites (cloning linkers) and "cleaver sequences" (as described elsewhere herein).

[00126] The nucleic acid molecule can be part of an expression cassette. The expression cassette can comprise a promoter, an open reading frame comprising the disclosed nucleic acid molecules, and a 3' untranslated region. The expression cassette can be used to direct a host cell's machinery to produce the disclosed fusion proteins.

[00127] Vectors comprising the disclosed nucleic acid molecules are also provided.

Suitable vectors include, for example, bacterial vectors, viral vectors, naked DNA vectors, and naked RNA vectors.

[00128] NKX3.1-PAP fusion proteins

[00129] Disclosed herein are fusion proteins comprising an NK3 homeobox 1 (NKX3.1) polypeptide and a PAP polypeptide.

[00130] Suitable NKX3.1 polypeptides include full length NKX3.1 (amino acids 1-234 of NKX3.1; "NKX3.1"). In some embodiments, the NKX3.1 polypeptide can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 as set forth in SEQ ID NO:29. In some embodiments, the NKX3.1 polypeptide can consist of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 as set forth in SEQ ID NO:29. In some embodiments, the NKX3.1 polypeptide can consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 as set forth in SEQ ID NO:29.

[00131] Suitable PAP polypeptides include amino acids 33-386 of PAP ("ΡΑΡ33-386")· Thus, in some embodiments, the PAP polypeptide can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14. In some embodiments, the PAP polypeptide can consist of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14. In some embodiments, the PAP polypeptide can consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14.

[00132] The NKX3.1 polypeptide can be fused to the N-terminus or C-terminus of the PAP polypeptide. Preferably, the NKX3.1 polypeptide can be fused to the N-terminus of the PAP polypeptide.

[00133] The fusion protein can comprise, consist of, or consist essentially of a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14.

[00134] The fusion protein can comprise, consist of, or consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP33-386 as set forth in amino acid residues 89 to 678 of SEQ ID NO:27.

[00135] The disclosed fusion proteins can further comprise a signal sequence. In some embodiments, the fusion protein can further comprise a signal sequence, wherein the signal sequence is in translational reading frame with the NKX3.1 polypeptide and the PAP polypeptide. Suitable signal sequences include, for example, ActANlOO (as set forth in SEQ ID NO:60), ActANlOO* (as set forth in SEQ ID NO:2), LL0441 (as set forth in SEQ ID NO:49), LL0441APEST (as set forth in SEQ ID NO:51), and ΙΧ0441Δ26 (as set forth in SEQ ID NO:53). In some embodiments, the signal sequence can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO as set forth in SEQ ID NO:60. In some embodiments, the signal sequence can comprise an amino acid sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2. Accordingly, in some embodiments, the fusion protein can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO*- NKX3.1-PAP33-386 as set forth in SEQ ID NO:27.

[00136] The disclosed fusion proteins can be expressed in a number of suitable host cells as disclosed elsewhere herein. In some embodiments, for example, the fusion protein can be expressed in a bacterium, such as Listeria monocytogenes or a genetically modified form thereof.

[00137] Also disclosed are nucleic acid molecules encoding an NKX3.1-PAP fusion protein. The disclosed nucleic acid molecules can encode any of the NKX3.1-PAP fusion proteins disclosed herein.

[00138] The disclosed nucleic acid molecules can encode an NKX3.1-PAP fusion protein, wherein the NKX3.1 polypeptide is encoded by a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3.1 polynucleotide as set forth in SEQ ID NO:28. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00139] The disclosed nucleic acid molecules can encode an NKX3.1-PAP fusion protein, wherein the PAP polypeptide is encoded by a polynucleotide that is at least i) 90% identical, ii) 95%) identical, iii) 99% identical, or iv) 100%> identical to the PAP 33.386 polynucleotide as set forth in SEQ ID NO: 13. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00140] The nucleic acid molecule can encode an NKX3. l-PAP ₃₃ .386 fusion protein. In some embodiments, for example, the nucleic acid molecule can comprise a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%> identical to the NKX3.1 polynucleotide as set forth in SEQ ID NO:28 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the PAP 33-386 polynucleotide as set forth in SEQ ID NO: 13. In some aspects, the nucleic acid molecule is operably linked to a promoter. [00141] The nucleic acid molecule can further comprise a promoter, a signal sequence, or both, wherein the promoter, signal sequence, or both are operably linked with the nucleotide sequence encoding the NKX3.1 polypeptide and the nucleotide sequence encoding the PAP polypeptide. Suitable promoters include, for example, actA (as set forth in SEQ ID NO:21) or ly (as set forth in SEQ ID NO:47). The promoter can comprise, for example, a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to an actA promoter as set forth in SEQ ID NO:21. Suitable signal sequences include, for example, ActANlOO (as set forth in SEQ ID NO:59), ActANlOO* (as set forth in SEQ ID NO: 1), LL0441 (as set forth in SEQ ID NO:48), LL0441APEST (as set forth in SEQ ID NO:50), and LL0441A26 (as set forth in SEQ ID NO:52). The signal sequence can comprise, for example, a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth in SEQ ID NO: l . Accordingly, in some embodiments, the nucleic acid molecule encoding the NKX3.1- PAP fusion protein can comprise, consist of, or consist essentially of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to actA- ActAN100*-NKX3.1-PAP 33-386 as set forth in SEQ ID NO:26.

[00142] The nucleic acid molecules can further comprise additional nucleic acid sequences including, but not limited to, restriction endonuclease cleavage sites (cloning linkers).

[00143] The nucleic acid molecule can be part of an expression cassette. The expression cassette can comprise a promoter, an open reading frame comprising the disclosed nucleic acid molecules, and a 3' untranslated region. The expression cassette can be used to direct a host cell's machinery to produce the disclosed fusion proteins.

[00144] Vectors comprising the disclosed nucleic acid molecules are also provided.

Suitable vectors include, for example, bacterial vectors, viral vectors, naked DNA vectors, and naked RNA vectors.

[00145] ActAN100*-SSX2 fusion proteins

[00146] Disclosed herein are fusion proteins comprising an ActANlOO* polypeptide and an SSX2 polypeptide.

[00147] Suitable SSX2 polypeptides include amino acids 1-234 of SSX2 ("SSX2" or "SSX2i _-2 34") and amino acids 2-234 of SSX2 ("SSX2 _2-234 ")- In some embodiments, the SSX2 polypeptide can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10. In some embodiments, the SSX2 polypeptide can consist of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10. In some embodiments, the SSX2 polypeptide can consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10.

[00148] The ActANlOO* polypeptide can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2.

[00149] In some embodiments, the fusion protein can comprise an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10. In some embodiments, the fusion protein can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:31.

[00150] Other suitable signal sequences include, for example, ActANlOO (as set forth in SEQ ID NO:60), LL0441 (as set forth in SEQ ID NO:49), LL0441APEST (as set forth in SEQ ID NO:51), and ΙΧ0441Δ26 (as set forth in SEQ ID NO:53).

[00151] The disclosed fusion proteins can be expressed in a number of suitable host cells as disclosed elsewhere herein. In some embodiments, for example, the fusion protein can be expressed in a bacterium, such as Listeria monocytogenes or a genetically modified form thereof.

[00152] Also disclosed are nucleic acid molecules encoding an ActAN100*-SSX2 fusion protein. In some embodiments, the nucleic acid molecule encoding the ActAN100*-SSX2 fusion protein can comprise, consist of, or consist essentially of an ActANlOO*

polynucleotide at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth in SEQ ID NO: 1 and a SSX2 polynucleotide at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the SSX2 as set forth in SEQ ID NO:9. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the nucleic acid molecule encoding the ActAN100*-SSX2 fusion protein can comprise, consist of, or consist essentially of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to actA- ActAN100*-SSX2 as set SEQ ID NO:30. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00153] Other suitable suitable signal sequences include, for example, ActANlOO (as set forth in SEQ ID NO:59), LL0441 (as set forth in SEQ ID NO:48), LL0441APEST (as set forth in SEQ ID NO:50), and LL0441A26 (as set forth in SEQ ID NO:52).

[00154] The nucleic acid molecules can further comprise additional nucleic acid sequences including, but not limited to, restriction endonuclease cleavage sites (cloning linkers). The nucleic acid molecules can be generated using a number of suitable restriction endonucleases, wherein the endonuclease cleavage site(s) may remain in the final nucleic acid molecule.

[00155] The nucleic acid molecule can be part of an expression cassette. The expression cassette can comprise a promoter, an open reading frame comprising the disclosed nucleic acid molecules, and a 3' untranslated region. The expression cassette can be used to direct a host cell's machinery to produce the disclosed fusion proteins.

[00156] Vectors comprising the disclosed nucleic acid molecules are also provided.

Suitable vectors include, for example, bacterial vectors, viral vectors, naked DNA vectors, and naked RNA vectors.

[00157] ActANlOO-PAP fusion proteins

[00158] Disclosed herein are fusion proteins comprising an ActANlOO polypeptide and an PAP polypeptide.

[00159] Suitable PAP polypeptides include amino acids 30-386 of PAP ("PAP ₃ o _-386 ")- ^In some embodiments, the PAP polypeptide can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₀ - ₃ 86 as set forth in amino acid residues 103-459 of SEQ ID NO:33. In some embodiments, the PAP polypeptide can consist of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99%) identical, or iv) 100%) identical to PAP _30-3 86 as set forth in amino acid residues 103- 459 of SEQ ID NO:33. In some embodiments, the PAP polypeptide can consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _30-38 6 as set forth in amino acid residues 103-459 of SEQ ID NO:33.

[00160] Suitable signal sequences, for example, ActANlOO (as set forth in SEQ ID

NO:60), ActANlOO* (as set forth in SEQ ID NO: 2), LL0441 (as set forth in SEQ ID

NO:49), LL0441APEST (as set forth in SEQ ID NO:51), and ΙΧ0441Δ26 (as set forth in SEQ ID NO:53). In some embodiments, the ActANlOO polypeptide can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to amino acid residues 1 to 100 of SEQ ID NO:33. In other embodiments, the ActANlOO* polypeptide can comprise an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2.

[00161] The ActANlOO-PAP fusion proteins can further comprise an SL8 polypeptide. The SL8 polypeptide is a T-cell epitope tag ("SIINFEKL" from chicken ovalbumin

(OVA257-264)), which can be used to assist in the detection of an attached antigen by for example, Western blot. SL8 is a class I (Kb)-restricted peptide epitope that is presented by the class I MHC molecule, H-2Kb, relevant to the C57/BL6 mouse.

[00162] In some embodiments, the ActANlOO-PAP fusion protein can comprise, consist of, or consist essentially of, an ActANlOO polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to amino acid residues 1 to 100 of SEQ ID NO:33 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₀ -386 as set forth in amino acid residues 103-459 of SEQ ID NO:33. In some embodiments, the ActANlOO-PAP fusion protein can comprise, consist of, or consist essentially of, an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _30- 386 as set forth in amino acid residues 103-459 of SEQ ID NO:33. In some embodiments, the fusion protein can comprise, consist of, or consist essentially of, an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO- PAP _30-3 86 as set forth in amino acid residues 1-459 of SEQ ID NO:33. In some embodiments, the fusion protein can comprise, consist of, or consist essentially of an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100-PAP _30-38 6-SL8 as set forth in SEQ ID NO:33.

[00163] The disclosed fusion proteins can be expressed in a number of suitable host cells as disclosed elsewhere herein. In some embodiments, for example, the fusion protein can be expressed in a bacterium, such as Listeria monocytogenes or a genetically modified form thereof.

[00164] Also disclosed are nucleic acid molecules encoding an ActANlOO-PAP fusion proteins. In some embodiments, the nucleic acid molecule encoding the ActANlOO-PAP fusion proteins can comprise, consist of, or consist essentially of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to actA- ActAN 100-PAP 30-386-SL8 as set SEQ ID NO:32. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00165] Suitable suitable signal sequences include, for example, ActANlOO (as set forth in SEQ ID NO:59), LL0441 (as set forth in SEQ ID NO:48), LL0441APEST (as set forth in SEQ ID NO:50), and LL0441A26 (as set forth in SEQ ID NO:52).

[00166] The nucleic acid molecules can further comprise additional nucleic acid sequences including, but not limited to, restriction endonuclease cleavage sites (cloning linkers). The nucleic acid molecules can be generated using a number of suitable restriction endonucleases, wherein the endonuclease cleavage site(s) may remain in the final nucleic acid molecule.

[00167] The nucleic acid molecule can be part of an expression cassette. The expression cassette can comprise a promoter, an open reading frame comprising the disclosed nucleic acid molecules, and a 3' untranslated region. The expression cassette can be used to direct a host cell's machinery to produce the disclosed fusion proteins.

[00168] Vectors comprising the disclosed nucleic acid molecules are also provided.

Suitable vectors include, for example, bacterial vectors, viral vectors, naked DNA vectors, and naked RNA vectors.

[00169] Host cells comprising nucleic acid molecules encoding the immunogenic polypeptides

[00170] Host cells comprising any of the disclosed nucleic acid molecules are also provided. Also disclosed are host cells expressing fusion proteins encoded by any of the disclosed nucleic acid molecules.

[00171] Suitable host cells include, for example, bacterium. Host cells can be attenuated, commensal, and/or killed but metabolically active. In an exemplary embodiment, the host cell can be an attenuated, commensal, and/or killed but metabolically active bacterium.

Suitable bacterium include, but are not limited to, Listeria monocytogenes, Shigella flexneri, Escherichia coli, Yersinia enterocolitica, Salmonella typhimurium, Salmonella typhi or mycobacterium species, or modified forms thereof. In some embodiments, for example, the host cell can be Listeria monocytogenes or a modified form thereof. Modifications include mutations, alterations, and other genetic changes/variations, as well as heat-treatment or chemical modification, which reduce the toxicity of the host cell to a subject. The bacterium can be modified, for example, to reduce binding to cells within a subject, reduce spread from one cell to another within a subject, reduce extracellular growth in a subject, or reduce intracellular growth in a subject.

[00172] Bacterial strains suitable as host cells include those described in U.S. Patent App. No. 13/988,076 (U.S. Patent Publ. No. 2014/037662), herein incorporated by reference in its entirety. For example, the host cell can be a live-attenuated strain of L. monocytogenes which is genetically modified to comprise an attenuating mutation in actA and/or inlB, and preferably a deletion of all or a portion of actA and MB (referred to herein as "Lm

AactA/AMB"), and contains a nucleic acid molecule encoding the immunogenic fusion protein. In some embodiments, the Listeria monocytogenes can be an actA deletion (AactA) mutant, an actA insertion mutant, an inlB deletion {AinlB) mutant, an inlB insertion mutant, or a combination thereof. For example, the Listeria monocytogenes can be a AactA/AinlB mutant.

[00173] The host cells can comprise one or more of the disclosed nucleic acid molecules. The one or more mucleic acid molecules can be integrated into the host cell genome. Such host cells can contain nucleic acids that are under the control of host cell expression sequences and thereby do not require eukaryotic transcriptional or translational elements. The nucleic acid molecules can be integrated into the actA locus, MB locus or tRNA ^Arg locus. In some embodiments, the nucleic acid molecule can be integrated into the actA locus. In some embodiments, the nucleic acid molecule can be integrated into the B locus. In some embodiments, the nucleic acid molecule can be integrated into the tRNA ^Arg locus. Table 4 provides an exemplary list of host cells comprising nucleic acid molecules encoding immunogenic fusion proteins, in which the nucleic acid molecules are integrated into the host cell genome. The following list is intended to be exemplary only.

Table 4

Strain Background locus Antigen expression cassette

Lml l Lm AactA AinlB - -

DP-

Lm Ahly - -

L4027

actA ActAN100*-EGFRvIIIx5-SSX2

MB ActAN100*-EGFRvIIIx5-PAP ₃ 3-386

BH5258 Lm AactA AinlB

ActAN100*-EGFRvIIIx5-NKX3.1 ii _-234 - tRNA ^Arg

PSMA ₁ . _{20; 44} - ₁₃ 8, 169-750

actA ActAN100*-EGFRvIIIx5-SSX2

BH5290 Lm AactA AinlB MB ActAN100*-EGFRvIIIx5-PAP _33-386

tRNA ^Arg ActAN 100 * -EGFRvIIIx5 -NKX3.1 (R41 G)n. 234-PSMAi-20, 44-138, 169-750

MB ActAN100*- KX3.1-PAP ₃₃ -386

BH4598 Lm AactA AinlB

tRNA ^Arg ActAN100*-SSX2

MB ActAN100*- KX3.1-PAP ₃₃ .386

BH4602 Lm AactA AinlB

tRNA ^Arg ActAN100*-EGFRvIIIx5-SSX2

BH2868 Lm AactA AinlB tRNA ^Arg ActAN100*-PAP ₃ 3-386

PL1631 Lm AactA AinlB tRNA ^Arg ActANl 00*-EGFRvIIIxl -PAP33-386

PL 1629 Lm AactA AinlB tRNA ^Arg ActAN100*-EGFRvIIIx2-PAP ₃ 3-386

PL 1627 Lm AactA AinlB tRNA ^xg ActAN100*-EGFRvIIIx3-PAP ₃ 3-386

PL 1625 Lm AactA AinlB tRNA ^Arg ActANl 00*-EGFRvIIIx4-PAP ₃ 3-386

PL 1623 Lm AactA AinlB tRNA ^Axg ActANl 00*-EGFRvIIIx5-PAP ₃ 3-386

[00174] Conversely, the host cells can comprise a nucleic acid molecule encoding an immunogenic fusion protein wherein the nucleic acid molecule is within the host cell extrachromosomally. For example, one or more of the disclosed nucleic acid molecules encoding an immunogenic fusion protein can be inserted into an expression cassette on an episomal plasmid within the host cell.

[00175] In some embodiments, the host cells can comprise one or more of the disclosed nucleic acid molecules, wherein the nucleic acid molecule comprises:

a) one or more copies of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the SSX2 polynucleotide as set forth in SEQ ID NO: 9;

b) one or more copies of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the PAP ₃₃ . ₃₈ 6 polynucleotide as set forth in SEQ ID NO: 13;

c) one or more copies of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5, a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3.I _n .234 polynucleotide as set forth in SEQ ID NO:24, and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the PSMA1-20, 44-138, 109-750 as set forth in SEQ ID NO: 19;

d) one or more copies of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5, a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3.1(R41G)n-234 polynucleotide as set forth in SEQ ID NO: 17, and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to the PSMA1.20, 44-138, 109-750 as set forth in SEQ ID NO: 19;

e) a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3.1 polynucleotide as set forth in SEQ ID NO:28 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the PAP 33-386

polynucleotide as set forth in SEQ ID NO: 13;

f) an ActANlOO* polynucleotide at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth in SEQ ID NO: 1 and a SSX2 polynucleotide at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the SSX2 as set forth in SEQ ID NO: 9;

g) a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100-PAP ₃₀ -386-SL8 as set forth in SEQ ID NO:32; or

h) any combination thereof,

i) wherein the nucleic acid molecule is integrated into the actA locus, inlB locus or tRNA ^Arg locus, or wherein the nucleic acid molecule is inserted into an expression cassette on an episomal plasmid within the host cell.

[00176] In some aspects, the one or more nucleic acid molecules listed in a)-h) are operably linked to a promoter.

[00177] As disclosed elsewhere herein, the disclosed immunogenic fusion proteins and the nucleic acid molecules encoding the same can comprise one or more EGFRvIII polypeptides. Thus, "one or more copies of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5" includes, but is not limited to, immunogenic fusion proteins and the nucleic acid molecules encoding the same comprising 2, 3, 4, 5, or more copies of the EGFRvIII polypeptide.

[00178] In some embodiments, the host cells can comprise one or more of nucleic acid molecules, said nucleic acid molecules comprising:

a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3;

b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ -386 as set forth in SEQ ID NO: 11;

c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1n-234-PSMAi-2o, 44- 138, 169-750 as set forth in SEQ ID NO:22;

d) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G) _n . ₂ 34- PSMA 1.20, 44-138, 169-750 as set forth in SEQ ID NO: 15;

e) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:26;

f) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:30;

g) a nucleic acid sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANl 00-PAP ₃₀ - ₃₈ 6-SL8 as set forth in SEQ ID NO:32;

h) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIxl-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:34;

i) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx2-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 36; j) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx3-PAP ₃₃ -386 as set forth in SEQ ID NO:38;

k) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx4-PAP ₃₃ -386 as set forth in SEQ ID NO:40;

1) any combination thereof,

m) wherein the nucleic acid molecules are integrated into the actA locus, inlB locus or tRNA ^Arg locus, or wherein the nucleic acid molecules are inserted into an expression cassette on an episomal plasmid within the host cell.

[00179] In some aspects, the one or more nucleic acid molecules listed in a)-l) are operably linked to a promoter.

[00180] The host cell can comprise a nucleic acid molecule comprising: (a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3; (b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃ 86 as set forth in SEQ ID NO: 11; and (c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

EGFRvIIIx5-NKX3.1n-234-PSMAi-2o, 44-iss, 109-750 as set forth in SEQ ID NO:22. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some aspects, the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO: 3 can be integrated into the actA locus; the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 11 can be integrated into the inlB locus; and the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5- NKX3. lu-234-PSMAi.2o, 44-138, 109-750 as set forth in SEQ ID NO:22 can be integrated into the tRNA ^Arg locus. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00181] The host cell can comprise a nucleic acid molecule comprising: (a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3; (b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃₈ 6 as set forth in SEQ ID NO: 11; and (c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

EGFRvIIIx5-NKX3.1(R41G) ₁₁ .234-PSMA ₁ .2o, ₄₄ -m, 169-750 as set forth in SEQ ID NO: 15. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some aspects, the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO: 3 can be integrated into the actA locus; the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 11 can be integrated into the inlB locus; and the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5- NKX3.1(R41G)n-234-PSMA ₁ . ₂₀ , 44-m, 169-750 as set forth in SEQ ID NO: 15 can be integrated into the tRNA ^Arg locus. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00182] The host cells can comprise a nucleic acid molecule comprising: (a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 -PAP '33-386 as set forth in SEQ ID NO:26; and (b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some aspects, the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP ₃₃ - 386 as set forth in SEQ ID NO:26 can be integrated into the inlB locus and the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO: 3 can be integrated into the tRNA ^Arg locus. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00183] The host cells can comprise a nucleic acid molecule comprising: (a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 -PAP '33-386 as set forth in SEQ ID NO:26; and (b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:30. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some aspects, the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP ₃₃ - 386 as set forth in SEQ ID NO:26 can be integrated into the inlB locus and the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:30 can be integrated into the tRNA ^Arg locus. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00184] The host cell can comprise one or more nucleic acid molecules comprising a nucleic acid sequence encoding:

a) an EGFRvIII-SSX2 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

b) an EGFRvIII-PAP33.386 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33- 386 as set forth in SEQ ID NO: 14;

c) an EGFRvIII-NKX3.1 ₁₁ . ₂₃₄ -PSMA ₁ . _{20; 44} . _138; 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ΝΚΧ3.1 ιι _-234 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20; 4-138, 169-750 as set forth in SEQ ID NO:20;

d) an EGFRvIII-NKX3. l(R41G)ii _-2 34-PSMAi _-2 o, ₄ 4-i38, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1(R41G)n. 2 ₃₄ as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-2 o, 44-138, 169-750 as set forth in SEQ ID NO:20;

e) a NKX3. l-PAP ₃₃ .3s6 fusion protein, wherein the fusion protein comprises a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33-386 as set forth in SEQ ID NO: 14; f) an ActAN100*-SSX2 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10; or g) an ActAN100-PAP ₃ o-3 ₈ 6 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to ActANlOO* as set forth as SEQ ID NO:2 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to PAP _30- 3 ₈ 6 as set forth in amino acid residues 103-459 of SEQ ID NO:33;

[00185] wherein the nucleic acid molecules are integrated into the actA locus, inlB locus or tRNA ^Arg locus, or wherein the nucleic acid molecules are inserted into an expression cassette on an episomal plasmid within the host cell.

[00186] In some aspects, the one or more nucleic acid molecules listed in a)-g) are operably linked to a promoter.

[00187] The host cell can express one or more fusion proteins comprising:

[00188] an EGFRvIII-SSX2 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10; [00189] an EGFRvIII-PAP _33-386 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33-386 as set forth in SEQ ID NO: 14;

[00190] an EGFRvIII-NKX3.1 ₁₁ . ₂₃₄ -PSMA ₁ . _{20; 44} . _138; 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 n. ₂₃₄ as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _{-20; 4} 4- 138, 169-750 as set forth in SEQ ID NO:20;

[00191] an EGFRvIII-NKX3. l(R41G)n _-23 4-PSMAi _-2 o, 44-i ₃₈ , 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3. l(R41G)n _-234 as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20; 4-138, 169-750 as set forth in SEQ ID NO:20;

[00192] a NKX3.1-PAP _33-386 fusion protein, wherein the fusion protein comprises a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33-386 as set forth in SEQ ID NO: 14;

[00193] an ActAN100*-SSX2 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10; or [00194] an ActAN100-PAP _30-38 6 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃ o _-3 86 as set forth in amino acid residues 103-459 of SEQ ID NO:33;

[00195] The host cell can comprise one or more nucleic acid molecules comprising a nucleic acid sequence encoding:

a) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx5-SSX2 as set forth in amino acid residues 89 to 475 of SEQ ID NO:4 or an immunogenic fragment thereof; b) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx5-PAP _33-386 as set forth in amino acid residues 89 to 606 of SEQ ID NO: 12 or an immunogenic fragment thereof;

c) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1 ii _-23 4-PSMAi-2o, 44-i3 ₈ , 169-750 as set forth in amino acid residues 89 to 1177 of SEQ ID NO:23 or an immunogenic fragment thereof;

d) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G)ii _-23 4-PSMAi- 20, 44-i ₃₈ , 169-750 as set forth in amino acid residues 89 to 1177 of SEQ ID NO: 16 or an immunogenic fragment thereof;

e) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to NKX3. l-PAP _33-386 as set forth in amino acid residues 89 to 678 of SEQ ID NO:27 or an immunogenic fragment thereof; f) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO: 31 or an immunogenic fragment thereof;

g) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to ActAN100-PAP ₃₀ - ₃₈ 6 as set forth in amino acid residues 1-459 of SEQ ID NO:33 or an immunogenic fragment thereof; h) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIxl-PAP ₃₃ .3 ₈ 6 as set forth in amino acid residues 89 to 476 of SEQ ID NO:35 or an immunogenic fragment thereof;

i) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx2-PAP ₃₃ .3 ₈₆ as set forth in amino acid residues 89 to 509 of SEQ ID NO:37 or an immunogenic fragment thereof;

j) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx3-PAP ₃₃ .3 ₈₆ as set forth in amino acid residues 89 to 541 of SEQ ID NO:39 or an immunogenic fragment thereof;

k) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx4-PAP ₃₃ .3 ₈₆ as set forth in amino acid residues 89 to 573 of SEQ ID NO:41 or an immunogenic fragment thereof; or

1) any combination thereof;

m) wherein the nucleic acid molecules are integrated into the actA locus, inlB locus or tRNA ^Arg locus, or wherein the nucleic acid molecules are inserted into an expression cassette on an episomal plasmid within the host cell.

[00196] In some aspects, the one or more nucleic acid molecules listed in a)-l) are operably linked to a promoter.

[00197] The host cell can express one or more fusion proteins comprising:

a) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in amino acid residues 89 to 475 of SEQ ID NO:4 or an immunogenic fragment thereof; b) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ .3 ₈₆ as set forth in amino acid residues 89 to 606 of SEQ ID NO: 12 or an immunogenic fragment thereof;

c) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1 ii-234-PSMAi _-2 o, 44-i3 ₈ , 169-750 as set forth in amino acid residues 89 to 1 177 of SEQ ID NO:23 or an immunogenic fragment thereof;

an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G)ii _-23 4-PSMAi. 20, 44-138, 169-750 as set forth in amino acid residues 89 to 1 177 of SEQ ID NO: 16 or an immunogenic fragment thereof;

an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP ₃ 3.3 ₈₆ as set forth in amino acid residues 89 to 678 of SEQ ID NO:27 or an immunogenic fragment thereof; an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO: 31 or an immunogenic fragment thereof;

an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100-PAP ₃ o _-38 6 as set forth in amino acid residues 1-459 of SEQ ID NO:33 or an immunogenic fragment thereof; an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIxl-PAP _33-386 as set forth in amino acid residues 89 to 476 of SEQ ID NO:35 or an immunogenic fragment thereof;

an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx2-PAP _33-386 as set forth in amino acid residues 89 to 509 of SEQ ID NO:37 or an immunogenic fragment thereof;

an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx3-PAP _33-386 as set forth in amino acid residues 89 to 541 of SEQ ID NO:39 or an immunogenic fragment thereof;

an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx4-PAP _33-386 as set forth in amino acid residues 89 to 573 of SEQ ID NO:41 or an immunogenic fragment thereof; or

any combination thereof; [00198] Provided herein are recombinant Listeria bacterium that are modified to comprise any of the disclosed nucleic acid molecules. The nucleic acid molecule can be present in the Listeria extrachromosomally, or may be integrated into the bacterial genome. In some embodiments, for example, the host cell can be a Listeria monocytogenes AactA/AinlB mutant having a nucleic acid molecule encoding an immunogenic fusion protein integrated into the actA locus, inlB locus, or tRNA ^Arg locus. In some aspects, the nucleic acid molecule is operably linked to a promoter. The Listeria can be utilized as an expression platform for expressing the disclosed fusion proteins which are heterologous to the host cell. Such expression can lead to, for example, an immune response to the heterologous fusion protein in a subject containing the host cell.

[00199] Expression of the immunogenic fusion proteins are driven from the Lm actA promoter, which is highly induced when Lm has infected host cells. The actA gene resides in the PrfA regulon, a series of Lm virulence genes whose expression is controlled and induced by PrfA, a transcriptional activator protein that is induced in the context of the infected host cell. The expression cassette in the disclosed nucleic acid molecules exclusively utilizes Lm transcription, translation and secretion machinery and it does not contain any mammalian expression elements (such as promoter or terminator regions characteristic of mammalian expression systems). Therefore, unlike plasmid DNA- or viral-based vectors that must utilize the mammalian host cell machinery to express a designated gene of interest, and by definition, where gene transfer is a prerequisite for gene expression, Lm is a "self-contained" free-living organism. Within infected cells of the vaccinated host, the prokaryotic expression machinery of the disclosed host cells is utilized exclusively to synthesize the fusion protein within the host cell, which is subsequently secreted into the cytoplasm of an infect cell with the subject for antigen processing and presentation.

[00200] In some embodiments the host cell can comprise one or more nucleic acid molecules, wherein the one or more nucleic acid molecules comprises EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3, EGFRvIIIx5-PAP ₃₃ -386 as set forth in SEQ ID NO: 11, and

EGFRvIIIx5-NKX3.1(R41G) ₁₁ .234-PSMA ₁ .2o, 44-iss, m-750 as set forth in SEQ ID NO: 15. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00201] In some embodiments the host cell can comprise one or more nucleic acid molecules, wherein the one or more nucleic acid molecules consist of EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3, EGFRvIIIx5-PAP ₃₃ -386 as set forth in SEQ ID NO: 11, and EGFRvIIIx5-NKX3.1(R41G) ₁₁ -234-PSMA ₁ .2o, 44-iss, 169-750 as set forth in SEQ ID NO: 15. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00202] The host cells can be combined with a pharmaceutically acceptable excipient.

[00203] Also provided herein are vaccines comprising the disclosed host cells and a pharmaceutically acceptable excipient. The vaccines can be administered to a subject in an amount sufficient to elicit an appropriate immune response as disclosed herein.

[00204] Methods of eliciting an immune response

[00205] Also disclosed herein are methods of eliciting an immune response in a subject comprising administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein. In some embodiments, the method comprising administering to the subject a composition comprising a host cell, wherein the host cell expresses one or more of the fusion proteins disclosed herein.

[00206] As used herein, "a host cell" includes one or more host cells, wherein each host cell can comprise one or more nucleic acid molecules encoding an immunogenic fusion protein. In some embodiments, the host cells can comprise the same nucleic acid molecule(s) encoding an immunogenic fusion protein. For example, and without intending to be limiting, the method can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding EGFRvIII-SSX2. In some embodiments, the host cell can comprise different nucleic acid molecules encoding different immunogenic fusion proteins.

[00207] The methods can be carried out using any of the host cells disclosed herein, wherein the host cells comprise a nucleic acid molecule encoding an immunogenic fusion protein.

[00208] The methods of eliciting an immune response in a subject can comprise administering to the subject a composition comprising a host cell, said host cell comprising a one or more nucleic acid molecules, said nucleic acid molecules comprising a nucleic acid sequence encoding:

a) an EGFRvIII-SSX2 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

an EGFRvIII-PAP33.386 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14;

an EGFRvIII-NKX3.1 ₁₁ . ₂₃₄ -PSMA ₁ . _{20; 44} . _138; 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ΝΚΧ3.1 ιι _-234 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20; 4-138, 169-750 as set forth in SEQ ID NO:20;

an EGFRvIII-NKX3.1(R41G)ii _-2 34-PSMAi _-20 , 44-158, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1(R41G)n. ₂₃₄ as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20 , 44-i _38, 169-750 as set forth in SEQ ID NO:20;

a NKX3.1-PAP _33-386 fusion protein, wherein the fusion protein comprises a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33-386 as set forth in SEQ ID NO: 14; f) an ActAN100*-SSX2 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

g) an ActAN100*-PAP ₃ o-386 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to PAP ₃ o _-3 86 as set forth in amino acid residues 103-459 of SEQ ID NO:33; or

h) any combination thereof.

[00209] In some aspects, the one or more nucleic acid molecules listed in a)-h) are operably linked to a promoter.

[00210] Disclosed herein are methods of eliciting an immune response in a subject comprising, administering to the subject a composition comprising a host cell, wherein the host cell expresses one or more fusion proteins comprising:

a) an EGFRvIII-SSX2 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

b) an EGFRvIII-PAP _33-3 86 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33-386 as set forth in SEQ ID NO: 14;

c) an EGFRvIII-NKX3.1 ₁₁ . ₂₃₄ -PSMA ₁ . _{20; 44} . _138; 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 n _-23 4 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20; 4-138, 169-750 as set forth in SEQ ID NO:20;

an EGFRvIII-NKX3.1(R41G)ii _-2 34-PSMAi _-2 o _; 44-138, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1(R41G)n _-234 as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _{-20; 4} 4-i38, 169-750 as set forth in SEQ ID NO:20; a NKX3.1-PAP _33-3 86 fusion protein, wherein the fusion protein comprises a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

NKX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33-386 as set forth in SEQ ID NO: 14; an ActAN100*-SSX2 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

an ActAN100*-PAP _30-3 86 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to

ActANlOO* as set forth as SEQ ID NO:2 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₀ -386 as set forth in amino acid residues

103-459 of SEQ ID NO:33; or

h) any combination thereof.

[00211] In some embodiments, the methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein, wherein the nucleic acid molecule comprises one or more copies of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO: 5 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to the SSX2 polynucleotide as set forth in SEQ ID NO:9. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses an immunogenic fusion protein encoded by the nucleic acid molecules.

[00212] In some embodiments, the methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein, wherein the nucleic acid molecule comprises one or more copies of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO: 5 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to the PAP 33.386 polynucleotide as set forth in SEQ ID NO: 13. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses an immunogenic fusion protein encoded by the nucleic acid molecules.

[00213] In some embodiments, the methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein, wherein the nucleic acid molecule comprises one or more copies of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5, a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3.1 _n _ ₂ 34 polynucleotide as set forth in SEQ ID NO:24, and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to the PSMA i. ₂ o, 44-138, 109-750 as set forth in SEQ ID NO: 19. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses an immunogenic fusion protein encoded by the nucleic acid molecules. [00214] In some embodiments, the methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein, wherein the nucleic acid molecule comprises one or more copies of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5, a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3 (R41G) _n . ₂ 34 polynucleotide as set forth in SEQ ID NO: 17, and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to the PSMA i. ₂ o, 44-138, 109-750 as set forth in SEQ ID NO: 19. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses an immunogenic fusion protein encoded by the nucleic acid molecules.

[00215] In some embodiments, the methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein, wherein the nucleic acid molecule comprises a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3.1 polynucleotide as set forth in SEQ ID NO:28 and a

polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to the PAP 33.386 polynucleotide as set forth in SEQ ID NO: 13. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses an immunogenic fusion protein encoded by the nucleic acid molecules.

[00216] In some embodiments, the methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein, wherein the nucleic acid molecule comprises an ActANlOO* polynucleotide at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth in SEQ ID NO: l and a SSX2 polynucleotide at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the SSX2 as set forth in SEQ ID NO:9. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses an immunogenic fusion protein encoded by the nucleic acid molecules.

[00217] In some embodiments, the methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein, wherein the nucleic acid molecule comprises a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100-PAP ₃₀ -386-SL8 as set forth in SEQ ID NO:32. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses an immunogenic fusion protein encoded by the nucleic acid molecules.

[00218] In some embodiments, the methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein, wherein the nucleic acid molecule comprises any combination of the above nucleic acid molecules. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the immunogenic fusion protein encoded by the nucleic acid molecules.

[00219] The host cells can comprise one or more of the disclosed nucleic acid molecules, wherein the nucleic acid molecules comprise:

a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3;

b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 11;

c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1n-234-PSMAi-2o, 44- 138, 169-750 as set forth in SEQ ID NO:22;

d) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G) _n . ₂ 34- PSMA 1.20, 44-138, 169-750 as set forth in SEQ ID NO: 15;

e) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:26;

f) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:30;

g) a nucleic acid sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANl 00-PAP ₃₀ - ₃₈ 6-SL8 as set forth in SEQ ID NO:32; h) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIxl-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:34;

i) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx2-PAP ₃₃ -386 as set forth in SEQ ID NO: 36;

j) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx3-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:38;

k) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx4-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:40; or

1) a combination thereof.

[00220] In some aspects, the one or more nucleic acid molecules listed in a)-l) are operably linked to a promoter.

[00221] In some embodiments, the host cell expresses one or more fusion proteins, the one or more fusion proteins being expressed from a nucleic acid molecule comprising:

a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3;

b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 1 1 ;

c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1n-234-PSMAi-2o, 44- 138, 169-750 as set forth in SEQ ID NO:22;

d) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3. J(R4JG) ₁₁ . ₂₃ 4- PSMA j.2o, 44-138, 169-750 as set forth in SEQ ID NO: 15;

e) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:26; f) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:30;

g) a nucleic acid sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANl 00-PAP ₃₀ -386-SL8 as set forth in SEQ ID NO:32;

h) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIxl-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:34;

i) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx2-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 36;

j) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx3-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:38;

k) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx4-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:40; or

1) a combination thereof.

[00222] In some aspects, the one or more nucleic acid molecules listed in a)-l) are operably linked to a promoter.

[00223] The methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an

immunogenic fusion protein, wherein the nucleic acid molecule comprises a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00224] The methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an

immunogenic fusion protein, wherein the nucleic acid molecule comprises a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ _ ₃₈₆ as set forth in SEQ ID NO: 11. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00225] The methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an

immunogenic fusion protein, wherein the nucleic acid molecule comprises a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1 n^-PSMA^o, 44-iss, m-iso as set forth in SEQ ID NO:22. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00226] The methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an

immunogenic fusion protein, wherein the nucleic acid molecule comprises a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G) ₁₁ .234-PSMA ₁ . ₂ o, 44-ns, 109-750 as set forth in SEQ ID NO: 15. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00227] The methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an

immunogenic fusion protein, wherein the nucleic acid molecule comprises a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 -PAP '33-386 as set forth in SEQ ID NO:26. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00228] The methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an

immunogenic fusion protein, wherein the nucleic acid molecule comprises a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set SEQ ID NO:30. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules. [00229] The methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an

immunogenic fusion protein, wherein the nucleic acid molecule comprises a nucleic acid sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100-PAP ₃ o-386-SL8 as set SEQ ID NO:32. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00230] The method can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein, wherein the nucleic acid molecule comprises a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

EGFRvIIIxl -PAP 33_386 as set forth in SEQ ID NO:34. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00231] The method can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein, wherein the nucleic acid molecule comprises a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

EGFRvIIIx2-PAP 33-386 as set forth in SEQ ID NO:36. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00232] The method can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein, wherein the nucleic acid molecule comprises a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

EGFRvIIIx3-PAP 33-386 as set forth in SEQ ID NO:38. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00233] The method can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein, wherein the nucleic acid molecule comprises a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

EGFRvIIIx4-PAP 33.386 as set forth in SEQ ID NO:40. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00234] The method can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein, wherein the nucleic acid molecule comprises a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

EGFRvIIIx5-PAP 33-386 as set forth in SEQ ID NO: 11. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00235] As described previously herein, the nucleic acid molecules can be integrated into the actA locus, inlB locus, or tRNA ^Arg locus or can be inserted into an expression cassette on an episomal plasmid within the host cell.

[00236] In some embodiments, the methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises one or more nucleic acid molecules encoding immunogenic fusion proteins. Any of the herein described host cells comprising one or more nucleic acid molecules can be used in the methods.

[00237] The methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an

immunogenic fusion protein, wherein the nucleic acid molecule comprises: (a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3; (b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP 33-386 as set forth in SEQ ID NO: 11; and (c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

EGFRvIIIx5-NKX3.1n-234-PSMAi-2o, 44-ns, m-750 as set forth in SEQ ID NO:22. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some aspects, the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO: 3 can be integrated into the actA locus; the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP 33-386 as set forth in SEQ ID NO: 11 can be integrated into the inlB locus; and the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5- NKX3.1 π-234-PSMA 1-20, 44-138, 169-750 as set forth in SEQ ID NO:22 can be integrated into the tRNA ^Arg locus. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00238] The methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an

immunogenic fusion protein, wherein the nucleic acid molecule comprises: (a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3; (b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP 33-386 as set forth in SEQ ID NO: 11; and (c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

EGFRvIIIx5-NKX3.1(R41G) ₁₁ .234-PSMA ₁ .2o, 44-iss, m-750 as set forth in SEQ ID NO: 15. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some aspects, the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO: 3 can be integrated into the actA locus; the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃ 3-386 as set forth in SEQ ID NO: 11 can be integrated into the inlB locus; and the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5- NKX3.1(R41G) _n . ₂ 34-PSMA j. ₂₀ , ₄ 4-m, 169-750 as set forth in SEQ ID NO: 15 can be integrated into the tRNA ^Arg locus. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00239] The methods can comprise administering to the subject a composing comprising a host cell, wherein the host cell expresses one or more fusion proteins, the fusion proteins being expressed from a nucleic acid molecule comprising:

a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3;

b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5 -PAP 33-386 as set forth in SEQ ID NO: 11; and c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G) _n . ₂ 34- PSMAi-20, 44-138, 169-750 as set forth in SEQ ID NO: 15.

[00240] In some aspects, the one or more nucleic acid molecules listed in a)-c) are operably linked to a promoter.

[00241] In some embodiments, the one or more nucleic acid molecules consist of

EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3, EGFRvIIIx5-PAP 33-386 as set forth in SEQ ID NO: 11, and EGFRvIIIx5-NKX3.1(R41G) ₁₁ . ₂ 34-PSMA ₁ . ₂ o, ₄₄ -i38, m-750 as set forth in SEQ ID NO: 15. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00242] The methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an

immunogenic fusion protein, wherein the nucleic acid molecule comprises: (a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 -PAP '33-386 as set forth in SEQ ID NO:26; and (b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some aspects, the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP ₃₃ - 386 as set forth in SEQ ID NO:26 can be integrated into the inlB locus and the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO: 3 can be integrated into the tRNA ^Arg locus. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00243] The methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an

immunogenic fusion protein, wherein the nucleic acid molecule comprises: (a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP '33.386 as set forth in SEQ ID NO:26; and (b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:30. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some aspects, the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP ₃₃ - 386 as set forth in SEQ ID NO:26 can be integrated into the MB locus and the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:30 can be integrated into the tRNA ^Arg locus. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00244] Any of the host cells disclosed herein are suitable for use in the disclosed methods. For example, the host cell can be a live-attenuated strain of Listeria monocytogenes which is genetically modified to comprise an attenuating mutation in actA and/or inlB, and preferably a deletion of all or a portion of actA and inlB (referred to herein as "Lm

AactA/AinlB"), and contains a nucleic acid molecule encoding for an immunogenic fusion protein. In some embodiments, the Listeria monocytogenes can be an actA deletion mutant, an actA insertion mutant, an inlB deletion mutant, an inlB insertion mutant, or a combination thereof. For example, the Listeria monocytogenes can be a AactA/AinlB mutant.

[00245] Suitable modes of administering the composition to the subject include, but are not limited to, intravenously, orally, subcutaneously, intradermally, intramuscularly, intraperitoneally, transmucosally, nasal administration, or any combination thereof. In some embodiments, the administering step can be performed intravenously.

[00246] The host cell can be utilized as an expression platform for expressing the disclosed immunogenic fusion proteins within the subject, thus eliciting an immune response to the heterologous fusion protein in a subject containing the host cell. For example, the fusion protein can be expressed and secreted from the host cell in the cytosol of an infected cell within the subject. Infected cells include any cell within the subject that can take up the host cell. In some embodiments, the infected cell can be an antigen presenting cell. Antigen presenting cells (APCs) are cells of the immune system used for presenting antigen to T cells. APCs include dendritic cells, monocytes, macrophages, marginal zone Kupffer cells, microglia, Langerhans cells, T cells, and B cells. In some embodiments, the fusion protein can be expressed in one or more cells of the subject.

[00247] In some embodiments, methods can comprise administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding for fusion proteins comprising: an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in amino acid residues 89 to 475 of SEQ ID NO:4 or an immunogenic fragment thereof; an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP33.3 ₈ 6 as set forth in amino acid residues 89 to 606 of SEQ ID NO: 12 or an immunogenic fragment thereof;

an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1 ii-234-PSMAi _-2 o, 44-i3 ₈ , 169-750 as set forth in amino acid residues 89 to 1 177 of SEQ ID NO:23 or an immunogenic fragment thereof;

an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G)ii _-2 34-PSMAi- 20, 44-i3 ₈ , 169-750 as set forth in amino acid residues 89 to 1 177 of SEQ ID NO: 16 or an immunogenic fragment thereof;

an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to NKX3. l-PAP ₃₃ .3s6 as set forth in amino acid residues 89 to 678 of SEQ ID NO:27 or an immunogenic fragment thereof; an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIxl-PAP ₃₃ .3 ₈ 6 as set forth in amino acid residues 89 to 476 of SEQ ID NO:35 or an immunogenic fragment thereof;

an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx2-PAP ₃₃ .3 ₈ 6 as set forth in amino acid residues 89 to 509 of SEQ ID NO:37 or an immunogenic fragment thereof;

an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx3-PAP ₃₃ .3 ₈ 6 as set forth in amino acid residues 89 to 541 of SEQ ID NO:39 or an immunogenic fragment thereof;

an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx4-PAP ₃₃ .3 ₈ 6 as set forth in amino acid residues 89 to 573 of SEQ ID NO:41 or an immunogenic fragment thereof; or

j) any combination thereof.

[00248] In some aspects, the one or more nucleic acid molecules listed in a)-j) are operably linked to a promoter.

[00249] The disclosed methods can be used to elicit an EGFRvIII immune response, an SSX2 immune response, a PAP immune response, a KX3.1 immune response, a PSMA immune response, immunity against Listeria, or any combination thereof. Accordingly, provided are methods of eliciting an EGFRvIII immune response in a subject comprising administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein. Also provided are methods of eliciting an SSX2 immune response in a subject comprising administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein. Also provided are methods of eliciting a PAP immune response in a subject comprising administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein. Also provided are methods of eliciting an KX3.1 immune response in a subject comprising administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein. Also provided are methods of eliciting a PSMA immune response in a subject comprising administering to the subject a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein. Further provided are methods of eliciting immunity against Listeria in a subject comprising administering to the subject a composition comprising Listeria monocytogenes, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein.

[00250]

[00251] Methods of increasing expression of an antigenic peptide

[00252] Also disclosed herein are methods of increasing expression of an antigenic peptide comprising expressing in a host cell one or more of the disclosed nucleic acid molecules.

[00253] The methods of increasing expression of an antigenic polypeptide can comprise expressing in a host cell a nucleic acid molecule, said nucleic acid molecule comprising a nucleic acid sequence encoding: an EGFRvIII-SSX2 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

an EGFRvIII-PAP33.386 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33- 386 as set forth in SEQ ID NO: 14;

an EGFRvIII-NKX3.1 ₁₁ . ₂₃₄ -PSMA ₁ . _{20; 44} . _138; 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ΝΚΧ3.1 ιι _-234 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20; 4-138, 169-750 as set forth in SEQ ID NO:20;

an EGFRvIII-NKX3.1(R41G)ii _-2 34-PSMAi _-20 , 44-158, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1(R41G)n _-234 as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20 , ₄ 4-i ₃₈ , 169-750 as set forth in SEQ ID NO:20; a NKX3.1-PAP _33-386 fusion protein, wherein the fusion protein comprises a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to KX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14; f) an ActAN100*-SSX2 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

g) an ActAN100*-PAP ₃ o-386 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%> identical to PAP30-386 as set forth in amino acid residues 103-459 of SEQ ID NO:33; or

h) any combination thereof.

[00254] In some aspects, the one or more nucleic acid molecules listed in a)-h) are operably linked to a promoter.

[00255] The methods can be carried out using any of the nucleic acid molecules disclosed herein. In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule comprising one or more copies of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the SSX2

polynucleotide as set forth in SEQ ID NO:9. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule comprising one or more copies of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%> identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the PAP 33-386 polynucleotide as set forth in SEQ ID NO: 13. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule comprising one or more copies of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5, a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3.1 _n _ ₂₃₄ polynucleotide as set forth in SEQ ID NO:24, and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to the PSMA1-20, 44-138, w- 750 as set forth in SEQ ID NO: 19. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule comprising one or more copies of a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5, a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3.1(R41G) _U -234 polynucleotide as set forth in SEQ ID NO: 17, and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the PSMA1-20, 44-138, w- 750 as set forth in SEQ ID NO: 19. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule comprising a polynucleotide that is at least i) 90% identical, ii) 95%) identical, iii) 99% identical, or iv) 100%> identical to the NKX3.1 polynucleotide as set forth in SEQ ID NO:28 and a polynucleotide that is at least 90% identical to the PAP ₃₃ .386 polynucleotide as set forth in SEQ ID NO: 13. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00256] In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule comprising a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth in SEQ ID NO: l and a polynucleotide at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to the SSX2 as set forth in SEQ ID NO:9. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00257] In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule comprising a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANIOO-PAP ₃ o-386-SL8 as set forth in SEQ ID NO:32. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00258] In some embodiments, the methods can comprise expressing in a host cell any combination of the above nucleic acid molecules. The host cells can comprise one or more of the following nucleic acid molecules: a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3;

a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ -386 as set forth in SEQ ID NO: 11;

a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1n-234-PSMAi-2o, 44- 138, 169-750 as set forth in SEQ ID NO:22;

a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii)

99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G) _n . ₂ 34-

PSMA 1.20, 44-138, 169-750 as set forth in SEQ ID NO: 15;

a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii)

99% identical, or iv) 100% identical to NKX3.1-PAP ₃₃ . ₃₈₆ as set forth in SEQ

ID NO:26;

a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:30;

a nucleic acid sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANl 00-PAP ₃₀ - ₃₈ 6-SL8 as set forth in SEQ ID NO:32;

a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIxl-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:34;

a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx2-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 36;

a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx3-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:38; k) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx4-PAP ₃₃ -386 as set forth in SEQ ID NO:40; or

1) or a combination thereof.

[00260] In some aspects, the one or more nucleic acid molecules listed in a)-l) are operably linked to a promoter.

[00261] In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule comprising a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00262] In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule comprising a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ -386 as set forth in SEQ ID NO: 11. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00263] In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule comprising a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical \o EGFRvIIIx5-NKX3.1n-234-PSMA _L 20, 44-138, 169-750 as set forth in SEQ ID NO:22. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00264] In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule comprising a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G)ii _-234 - PSMAi _-20; 44-138, 169-750 as set forth in SEQ ID NO: 15. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00265] In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule comprising a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP ₃ 3. ₃₈₆ as set forth in SEQ ID NO:26. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00266] In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule comprising a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIxl-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:34. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00267] In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule comprising a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx2-PAP ₃₃ -386 as set forth in SEQ ID NO:36. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00268] In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule comprising a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx3-PAP ₃₃ -386 as set forth in SEQ ID NO:38. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00269] In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule comprising a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx4-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:40. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00270] In some embodiments, the methods can comprise expressing in a host cell a nucleic acid molecule comprising a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 11. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00271] As described previously herein, the nucleic acid molecules can be integrated into the actA locus, inlB locus, or tRNA ^Arg locus or can be inserted into an expression cassette on an episomal plasmid within the host cell.

[00272] In some embodiments, the methods can comprise expressing in a host cell one or more of the above nucleic acid molecules.

[00273] The methods can comprise expressing in a host cell a nucleic acid molecule comprising: (a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3; (b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 11; and (c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1 n^-PSMA^o, 44-iss, 169-750 as set forth in SEQ ID NO:22. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some aspects, the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO: 3 can be integrated into the actA locus; the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP 33-386 as set forth in SEQ ID NO: 11 can be integrated into the inlB locus; and the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

EGFRvIIIx5-NKX3.1n-234-PSMAi-2o, 44-ns, 109-750 as set forth in SEQ ID NO:22 can be integrated into the tRNA ^Arg locus. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00274] The methods can comprise expressing in a host cell a nucleic acid molecule comprising: (a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3; (b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP 33-386 as set forth in SEQ ID NO: 11; and (c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G) ₁₁ -234-PSMA ₁ - ₂ o, 44-ns, m-750 as set forth in SEQ ID NO: 15. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some aspects, the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO: 3 can be integrated into the actA locus; the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP 33-386 as set forth in SEQ ID NO: 11 can be integrated into the inlB locus; and the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

EGFRvIIIx5-NKX3.1(R41G) ₁₁ -234-PSMA ₁ -2o, ₄₄ -m, 169-750 as set forth in SEQ ID NO: 15 can be integrated into the tRNA ^Arg locus. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00275] The methods can comprise expressing in a host cell a nucleic acid molecule comprising: (a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP 33-386 as set forth in SEQ ID NO:26; and (b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some aspects, the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP 33-386 as set forth in SEQ ID NO:26 can be integrated into the MB locus and the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO: 3 thereof can be integrated into the tRNA ^Arg locus. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00276] The methods can comprise expressing in a host cell a nucleic acid molecule comprising: (a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP ₃₃ -386 as set forth in SEQ ID NO:26; and (b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:30. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some aspects, the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP 33-386 as set forth in SEQ ID NO:26 can be integrated into the MB locus and the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:30 can be integrated into the tRNA ^Arg locus. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00277] The disclosed methods can be performed in any host cell that supports, or can be configured to support, transcription of the disclosed nucleic acid molecules and expression of the antigenic polypeptide including, but not limited to, bacterial cells, viral cells, yeast cells, insect cells, and mammalian cells. The expressing step can be performed by introducing the nucleic acid molecule into a host cell and allowing the host cell machinery to produce the antigenic polypeptide. For example, the host cell can be a live-attenuated strain of Listeria monocytogenes which is genetically modified to comprise an attenuating mutation in actA and/or inlB, and preferably a deletion of all or a portion of actA and inlB (referred to herein as "Lm AactA/AinlB"), and contains a nucleic acid molecule encoding for an immunogenic fusion protein. In some embodiments, the Listeria monocytogenes can be an actA deletion mutant, an actA insertion mutant, an inlB deletion mutant, an inlB insertion mutant, or a combination thereof. For example, the Listeria monocytogenes can be a AactA/AinlB mutant.

[00278] Alternatively, the expressing step can be performed by administering the host cell to a cell of interest, wherein the antigenic polypeptide is produced within said cell of interest. In some embodiments, the expressing step can be performed by infecting a cell of interest with the host cell, wherein the antigenic polypeptide is produced within the cell of interest. In some embodiments, the expressing step can be performed by administering the host cell to a subject, wherein the antigenic polypeptide is produced within the subject.

[00279] The methods can comprise expressing in a host cell a nucleic acid molecule encoding for fusion proteins comprising:

a) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in amino acid residues 89 to 475 of SEQ ID NO:4 or an immunogenic fragment thereof; b) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP33.3 ₈ 6 as set forth in amino acid residues 89 to 606 of SEQ ID NO: 12 or an immunogenic fragment thereof;

c) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1 ii-234-PSMAi _-2 o, 44-i3 ₈ , 169-750 as set forth in amino acid residues 89 to 1 177 of SEQ ID NO:23 or an immunogenic fragment thereof;

d) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G)ii _-2 34-PSMAi- 20, 44-i3 ₈ , 169-750 as set forth in amino acid residues 89 to 1 177 of SEQ ID NO: 16 or an immunogenic fragment thereof;

e) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to NKX3. l-PAP ₃₃ .3s6 as set forth in amino acid residues 89 to 678 of SEQ ID NO:27 or an immunogenic fragment thereof; f) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIxl-PAP ₃₃ .3 ₈ 6 as set forth in amino acid residues 89 to 476 of SEQ ID NO:35 or an immunogenic fragment thereof;

g) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx2-PAP ₃₃ .3 ₈ 6 as set forth in amino acid residues 89 to 509 of SEQ ID NO:37 or an immunogenic fragment thereof; h) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx3-PAP33.3 ₈₆ as set forth in amino acid residues 89 to 541 of SEQ ID NO:39 or an immunogenic fragment thereof;

i) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx4-PAP ₃₃ .3 ₈₆ as set forth in amino acid residues 89 to 573 of SEQ ID NO:41 or an immunogenic fragment thereof; or

j) any combination thereof.

[00280] In some aspects, the one or more nucleic acid molecules listed in a)-j) are operably linked to a promoter.

[00281] Methods of treating cancer

[00282] Disclosed herein are methods of treating cancer in a subject in need thereof, said methods comprising administering to the subject a therapeutically effective amount of a composition comprising a host cell, wherein the host cell comprises one or more of the nucleic acids disclosed herein. In some embodiments, the host cells express one or more fusion proteins encoded by the one or more nucleic acid molecules. For example, the host cell can comprise one or more nucleic acid molecules comprising a nucleic acid sequence encoding:

a) an EGFRvIII-SSX2 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

b) an EGFRvIII-PAP33.3 ₈₆ fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33- 3 ₈ 6 as set forth in SEQ ID NO: 14;

c) an EGFRvIII-NKX3.111.234-PSMA1.20, ₄₄ - ₁₃₈ , 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 n _-23 4 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20; 4-138, 169-750 as set forth in SEQ ID NO:20;

an EGFRvIII-NKX3.1(R41G)ii _-2 34-PSMAi _-2 o _; 44-138, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1(R41G)n _-234 as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _{-20; 4} 4-i38, 169-750 as set forth in SEQ ID NO:20; a NKX3.1-PAP _33-3 86 fusion protein, wherein the fusion protein comprises a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

NKX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33-386 as set forth in SEQ ID NO: 14; an ActAN100*-SSX2 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10; or an ActAN100-PAP _30-3 86 fusion protein, wherein the fusion protein comprises an ActANlOO polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to

ActANl OO as set forth in amino acid residues 1 to 100 of SEQ ID NO:33 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _{30- 38} 6 as set forth in amino acid residues 103-459 of SEQ ID NO:33; or h) any combination thereof.

[00283] In some aspects, the one or more nucleic acid molecules listed in a)-h) are operably linked to a promoter.

[00284] Also disclosed are methods of treating cancer in a subject in need thereof, said method comprising administering to the subject a therapeutically effective amount of a composition comprising a host cell, wherein the host cell expresses one or more fusion proteins comprising:

a) an EGFRvIII-SSX2 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10;

b) an EGFRvIII-PAP _33-386 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33-386 as set forth in SEQ ID NO: 14;

c) an EGFRvIII-NKX3.1 ₁₁ . ₂₃₄ -PSMA ₁ . _{20; 44} . _138; 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ΝΚΧ3.1 ιι _-234 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _{-20; 44-} i _38; 169-750 as set forth in SEQ ID NO:20;

d) an EGFRvIII-NKX3. l(R41G)ii _-234 -PSMAi _-2 o, ₄ 4-i38, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1(R41G)n _-2 34 as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _{-20; 4} 4-i38, 169-750 as set forth in SEQ ID NO:20; e) a NKX3. l-PAP ₃₃ .3s6 fusion protein, wherein the fusion protein comprises a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

NKX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33-386 as set forth in SEQ ID NO: 14; f) an ActAN100*-SSX2 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10; or g) an ActAN100-PAP ₃ o-3 ₈ 6 fusion protein, wherein the fusion protein comprises an ActANlOO polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to

ActANlOO as set forth in to amino acid residues 1 to 100 of SEQ ID NO:33 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _30- 3 ₈₆ as set forth in amino acid residues 103-459 of SEQ ID NO:33; or h) any combination thereof.

[00285] In some embodiments, the host cell expresses (a), (b), and (d).

[00286] In some embodiments, the one or more nucleic acid molecules can comprise a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the one or more nucleic acid molecules can comprise a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIxl -PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:34. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the one or more nucleic acid molecules can comprise a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx2-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:36. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the one or more nucleic acid molecules can comprise a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx3-PAP ₃₃ -386 as set forth in SEQ ID NO:38. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the one or more nucleic acid molecules can comprise a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx4-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:40. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the one or more nucleic acid molecules can comprise a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 11. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the one or more nucleic acid molecules can comprise a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1 n^-PSMA^o, 44-iss, m-750 as set forth in SEQ ID NO:22. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the one or more nucleic acid molecules can comprise a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%> identical to EGFRvIIIx5-NKX3.1(R41G) ₁₁ . ₂₃ 4-PSMA ₁ .2o, ₄₄ -m, 169-750 as set forth in SEQ ID NO: 15. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the one or more nucleic acid molecules can comprise a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%> identical to NKX3.1-PAP ₃₃ . ₃ 86 as set forth in SEQ ID NO:26. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the one or more nucleic acid molecules can comprise a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:30. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the one or more nucleic acid molecules can comprise a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%> identical to ActAN100-PAP ₃₀ . ₃ 86-SL8 as set forth in SEQ ID NO:32. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the one or more nucleic acid molecules can comprise any combination thereof. The host cell can expresses the fusion protein encoded by any of the above nucleic acid molecules.

[00287] In some aspects, the methods comprising administering to the subject a therapeutically effective amount of a composition comprising a host cell, wherein the host cell expresses one or more fusion proteins, the fusion proteins being expressed from a nucleic acid molecule comprising:

a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3;

b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 11; and

c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G) _n . ₂ 34- PSMA^o, 44-138, 169-750 as set forth in SEQ ID NO: 15.

[00288] In some aspects, the one or more nucleic acid molecules listed in a)-c) are operably linked to a promoter.

[00289] In some embodiments, the nucleotide sequences can be operably lined to an ActA promoter. The ActA promoter can have the sequence set forth as SEQ ID NO:21.

[00290] In some apsects, the fusion proteins are expressed from a nucleic acid molecule consisting of:

a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3;

b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ -386 as set forth in SEQ ID NO: 11; and

c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G) _n . ₂ 34- PSMAi-20, 44-138, 169-750 as set forth in SEQ ID NO: 15.

[00291] In some aspects, the one or more nucleic acid molecules listed in a)-c) are operably linked to a promoter. [00292] In some embodiments, the nucleotide sequences can be operably lined to an ActA promoter. The ActA promoter can have the sequence set forth as SEQ ID NO:21.

[00293] In some aspects, the fusion proteins are expressed from a nucleic acid molecule consisting of EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3, EGFRvIIIx5-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 11, and EGFRvIIIx5-NKX3.1(R41G) ₁₁ .234-PSMA ₁ . ₂ o, ₄₄ -m, 169-750 as set forth in SEQ ID NO: 15. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00294] The host cells can comprise the nucleic acid molecules integrated into the host cell genome. Such host cells contain nucleic acids that are under the control of host cell expression sequences and thereby do not require eukaryotic transcriptional or translational elements. The nucleic acid molecule can be integrated into the actA locus, inlB locus or tRNA ^Arg locus. In some embodiments, the nucleic acid molecule can be integrated into the actA locus. In some embodiments, the nucleic acid molecule can be integrated into the inlB locus. In some embodiments, the nucleic acid molecule can be integrated into the tRNA ^Arg locus. The host cells can comprise the nucleic acid molecule encoding the fusion protein wherein the nucleic acid molecule is within the host cell extrachromosomally. For example, one or more of the disclosed nucleic acid molecules encoding an immunogenic fusion protein can be inserted into an expression cassette on an episomal plasmid within the host cell.

[00295] The methods can comprise administering to the subject a therapeutically effective amount of a composition comprising a host cell, wherein the host cell comprises one or more nucleic acid molecules comprising: (a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3; (b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 11; and (c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3. lu-234-PSMAi.2o, 44-138, 109-750 as set forth in SEQ ID NO:22. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some aspects, the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3 can be integrated into the actA locus; the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 11 can be integrated into the inlB locus; and the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1 n^-PSMA^o, 44-iss, 169-750 as set forth in SEQ ID NO:22 can be integrated into the tRNA ^Arg locus. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00296] The methods can comprise administering to the subject a therapeutically effective amount of a composition comprising a host cell, wherein the host cell comprises one or more nucleic acid molecules comprising: (a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3; (b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 11; and (c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G) ₁₁ .234-PSMA ₁ . ₂ o, 44-iss, m-750 as set forth in SEQ ID NO: 15. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some aspects, the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3 can be integrated into the actA locus; the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 11 can be integrated into the inlB locus; and the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G) ₁₁ . ₂₃ 4-PSMA ₁ .2o, 44-ns, m-750 as set forth in SEQ ID NO: 15 can be integrated into the tRNA ^Arg locus. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00297] The methods can comprise administering to the subject a therapeutically effective amount of a composition comprising a host cell, wherein the host cell comprises one or more nucleic acid molecules comprising: (a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:26; and (b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some aspects, the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:26 can be integrated into the inlB locus and the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO: 3 can be integrated into the tRNA ^Arg locus. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00298] The methods can comprise administering to the subject a therapeutically effective amount of a composition comprising a host cell, wherein the host cell comprises one or more nucleic acid molecules comprising: (a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:26; and (b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO:30. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some aspects, the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:26 can be integrated into the inlB locus and the nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO:30 can be integrated into the tRNA ^Arg locus. In some aspects, the nucleic acid molecule is operably linked to a promoter.

[00299] PAP is one of the major proteins secreted by prostate columnar epithelium cells, both benign and malignant. The efficacy of PAP as an agent in immunotherapy was validated in the 2010 FDA approval of sipuleucel-T (Provenge ^® ), an autologous cellular immunotherapy that targets PAP as a treatment for advanced prostate cancer.

[00300] PSMA is a 100 kDA type II transmembrane glycoprotein with folate hydrolase and neurocarboxypeptidase activity. A nonsecretory, integral cell-surface membrane protein, PSMA is expressed in virtually all prostate cancers, with expression increasing progressively in higher-grade malignancies, metastatic disease and castration-resistant prostate cancer. The role of PSMA in prostate cancer is unknown, however the expression of PSMA correlates with disease progression, which suggests that PSMA has a functional role in the progression of prostate cancer. PSMA is also expressed in the neovasculature of solid tumors but not in normal vasculature. Although the role in neovasculature is unknown, it is possible that the folate hydrolase activity of PSMA is important in facilitating vasculogenesis in epithelial tissues.

[00301] SSX proteins are cancer-testis antigens (CTAs) representing a superfamily of highly homologous CTAs with nuclear localization, restricted expression in HLA Class I- deficient testis or ovary germline cells, and frequent overexpression in tumors of various histologic origins, especially in advanced- stage cancer. The expression of SSX proteins has been associated with stem cell migration, which suggests that it plays an important biological role for the metastatic phenotype. Because germ cells do not express Class I MHC molecules, they are protected from bystander autoimmunity. The overexpression of SSX2 in cancer cells and its limited expression in normal HLA Class I-expressing cells, make SSX2 a particularly attractive immunotherapy target for T-cell-based strategies. CTAs are normally expressed only in germ cells of the testis and have been shown to be spontaneously immunogenic in cancer patients. The ectopic expression of CTA in cancer tissue make these proteins ideal immunotherapy targets. Importantly, SSX2 was selected as an immune target for prostate cancer since IgG responses and CD8 ⁺ T cells specific for SSX-2 can be detected in prostate cancer patients, and expression has been demonstrated in advanced prostate cancer.

[00302] KX3.1 is a homeobox protein and maps to the minimal region of human chromosome hp21. KX3.1 is required for normal prostate development and is associated with all aspects of embryonic prostate development, neonatal differentiation, and adult function. It is the earliest known marker of prostate formation and continues to be expressed at all stages of prostate differentiation and in adulthood. A tissue-specific regulatory gene, KX3.1 is essential to normal morphogenesis and function of the prostate whereas its inactivation leads to prostatic epithelial hyperplasia and dysplasia that model a preneoplastic condition. KX3.1 marks a population of luminal cells with stem-like properties that persists in the prostate after androgen ablation. Importantly, these castration-resistant NKX3.1- expressing cells (CARNs) were shown to act as cells of origin for prostate cancer, since deletion of KX3.1 -expressing cells rendered prostate tumors unable to progress after androgen ablation and testosterone depletion. KX3.1 's unique overexpression on CARNs opens up the possibility to target the direct precursors of prostate CSC by vaccinating against this antigen. In addition, human NKX3.1 was recently identified as 1 of 7 prostate cancer susceptibility loci through a genome-wide association screen, making it an extremely attractive new antigenic target for immunotherapy of prostate cancer. Recent analyses indicate that low levels of NKX3.1 can be demonstrated in nearly all prostate cancers and metastases examined. Thus there appears to be a selection for reduction, but not loss, of NKX3.1 expression throughout cancer progression.

[00303] EGFR is a receptor tyrosine kinase critical for cell growth and survival. The EGFR gene is frequently overexpressed or mutated in human cancers, including head and neck, colon, pancreas, breast, ovary, kidney, and malignant gliomas. EGFRvIII results from a 267 amino acid deletion and the fusion of exon 1 with exon 8, yielding a tumor-specific peptide with a novel glycine at the junction. Patients with EGFRvIII-expressing breast cancers have detectable humoral and cellular immune responses against this peptide, suggesting that it serves as an immunogenic neoantigen. The EGFRvIII repeat sequence was included in the disclosed immunogenic fusion proteins due to its correlation with higher expression of the fusion proteins (PAP, PSMA, SSX2, and KX3.1) and higher antigen- specific immune responses to the prostate cancer-relevant antigens. As native EGFR is required for signal transduction in normal-functioning cell populations, it is important to note that the disclosed immunogenic fusion proteins contain only the 21 amino acid segment of the EGVRvIII neoantigenic region expressed by deletion of exons 2 to 7 in tumor cells.

[00304] Accordingly, suitable cancers that can be treated with the disclosed methods include EGFRvIII-expressing cancer, a SSX2-expressing cancer, a PAP-expressing cancer, a KX3.1 -expressing cancer, a PSMA-expressing cancer, or any combination thereof.

Preferably, the cancer is prostate cancer.

[00305] Any of the host cells disclosed herein are suitable for use in the disclosed methods. For example, the host cell can be Listeria monocytogenes. In a preferred aspect, the host cell can be a live-attenuated strain of Listeria monocytogenes which is genetically modified to comprise an attenuating mutation in actA and/or inlB, and preferably a deletion of all or a portion of actA and MB (referred to herein as "Lm AactA/ AinlB"), and contains a nucleic acid molecule encoding for one or more of the disclosed immunogenic fusion proteins. In some embodiments, the Listeria monocytogenes can be an actA deletion (AactA) mutant, an actA insertion mutant, an inlB deletion {AinlB) mutant, an inlB insertion mutant, or a combination thereof. For example, the Listeria monocytogenes can be a AactA/AinlB mutant.

[00306] The host cell can be utilized as an expression platform for expressing the immunogenic fusion proteins encoded by the nucleic acid molecules within the subject, thus eliciting an anti-tumor response to EGFRvIII-expressing tumor cells, SSX2-expressing tumor cells, PAP-expressing tumor cells, KX3.1 -expressing tumor cells, and/or PSMA-expressing tumor cells. The fusion protein can be expressed and secreted from the host cell in the cytosol of an infected cell within the subject. Infected cells include any cell within the subject that can take up the host cell. In some embodiments, the infected cell can be an antigen presenting cell. [00307] The host cell can comprise one or more nucleic acid molecules comprising a nucleic acid sequence encoding an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in amino acid residues 89 to 475 of SEQ ID NO:4. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00308] The host cell can comprise one or more nucleic acid molecules comprising a nucleic acid sequence encoding an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ .3 ₈₆ as set forth in amino acid residues 89 to 606 of SEQ ID NO: 12. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00309] The host cell can comprise one or more nucleic acid molecules comprising a nucleic acid sequence encoding an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3. l n.234-PSMAi.2o, 44- 138, 169-750 as set forth in amino acid residues 89 to 1 177 of SEQ ID NO:23. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00310] The host cell can comprise one or more nucleic acid molecules comprising a nucleic acid sequence encoding an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G)n. ₂ 34- PSMAi-20, 44-i3 ₈ , 169-750 as set forth in amino acid residues 89 to 1 177 of SEQ ID NO: 16. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some

embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00311] The host cell can comprise one or more nucleic acid molecules comprising a nucleic acid sequence encoding an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to NKX3.1-PAP ₃₃ .3 ₈₆ as set forth in amino acid residues 89 to 678 of SEQ ID NO:27. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00312] The host cell can comprise one or more nucleic acid molecules comprising a nucleic acid sequence encoding an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:31. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00313] The host cell can comprise one or more nucleic acid molecules comprising a nucleic acid sequence encoding an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%. identical to ActAN100-PAP _30- 386 as set forth in amino acid residues 1-459 of SEQ ID NO:33. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00314] The host cell can comprise one or more nucleic acid molecules comprising a nucleic acid sequence encoding an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-EGFRvIIIxl-PAP _33-386 as set forth in amino acid residues 89 to 476 of SEQ ID NO:35. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00315] The host cell can comprise one or more nucleic acid molecules comprising a nucleic acid sequence encoding an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-EGFRvIIIx2-PAP _33-386 as set forth in amino acid residues 89 to 509 of SEQ ID NO:37. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00316] The host cell can comprise one or more nucleic acid molecules comprising a nucleic acid sequence encoding an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-EGFRvIIIx3-PAP _33-386 as set forth in amino acid residues 89 to 541 of SEQ ID NO:39. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00317] The host cell can comprise one or more nucleic acid molecules comprising a nucleic acid sequence encoding an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-EGFRvIIIx4-PAP _33-386 as set forth in amino acid residues 89 to 573 of SEQ ID NO:41. In some aspects, the nucleic acid molecule is operably linked to a promoter. In some embodiments, the host cell expresses the fusion protein encoded by the nucleic acid molecules.

[00318] The host cell can comprise one or more nucleic acid molecules comprising a nucleic acid sequence encoding any combination of the above amino acid sequences. In some embodiments, the host cell expresses a combination of fusion proteins encoded by the one or more nucleic acid molecules. For example, the host cell can express one or more fusion proteins comprising:

a) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in amino acid residues 89 to 475 of SEQ ID NO:4;

b) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ .3 ₈₆ as set forth in amino acid residues 89 to 606 of SEQ ID NO: 12; and

c) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G)ii _-2 34-PSMAi- 20, 44-i3 ₈ , 169-750 as set forth in amino acid residues 89 to 1 177 of SEQ ID NO: 16.

[00319] In some aspects, the one or more nucleic acid molecules listed in a)-c) are operably linked to a promoter.

[00320] The host cell can express one or more fusion proteins consisting of:

a) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx5-SSX2 as set forth in amino acid residues 89 to 475 of SEQ ID NO:4;

b) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx5-PAP ₃₃ .3 ₈₆ as set forth in amino acid residues 89 to 606 of SEQ ID NO: 12; and

c) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G)ii _-2 34-PSMAi. 20, 44-i3 ₈ , 169-750 as set forth in amino acid residues 89 to 1 177 of SEQ ID NO: 16

[00321] The host cell can express one or more fusion proteins consisting of EGFRvIIIx5- SSX2 as set forth in amino acid residues 89 to 475 of SEQ ID NO:4, EGFRvIIIx5-PAP ₃ 3-3 ₈ 6 as set forth in amino acid residues 89 to 606 of SEQ ID NO: 12, and EGFRvIIIx5- NKX3.1(R41G)ii _-2 34-PSMAi _-20 , 44-i3 ₈ , 169-750 as set forth in amino acid residues 89 to 1 177 of SEQ ID NO: 16. [00322] The disclosed methods can further comprise measuring expression of EGFRvIII, SSX2, PAP, KX3.1, PSMA, or any combination thereof in a biological sample from the subject prior to administering the composition. Methods for measuring expression levels of EGFRvIII, SSX2, PAP, KX3.1, PSMA, or a combination thereof in a biological sample from the subject include, but are not limited to, immunohistochemistry (THC), Western Blotting, microscopy, immunoprecipitation, BCA assays, spectrophotometry, in vivo imaging, or any combination thereof. EGFRvIII, SSX2, PAP, KX3.1, and/or PSMA can be detected in biological samples including, but are not limited to, blood, lymph fluid, bone marrow, a solid tumor sample, or any combination thereof.

[00323] The compositions can further comprise a pharmaceutically acceptable excipient. For example, the host cells can be combined with any suitable buffer, including but not limited to, phosphate-buffered saline (PBS), and glycerol. In an exemplary embodiment, the composition can be formulated in Dulbecco's phosphate-buffered saline (PBS) and glycerol, stored frozen (at or below -60°C) until administration, and administered by intravenous (IV) infusion in sodium chloride over a suitable period of time. One skilled in the art would know that the period of time for administering the composition depends, in part, on the type of cancer, the severity of the cancer, and the subject's age, weight, etc. Preferably, the composition can be administered over a period of hours. For example, the composition can be administered over a 1-2 hour period. In other embodiments, the composition can be administered in less than 1-2 hours. In yet other embodiments, the composition can be administered in greater than 1-2 hours.

[00324] Treatment can include a single dose of the composition or multiple doses of the composition. Thus, the disclosed methods can comprise administering to the subject one or more doses of a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein. Factors that can determine the number of doses include, for example, the progression of the cancer, the severity of the cancer symptoms, the frequency of the cancer symptoms, tumor size, or any combination thereof. Without intent to be limiting, the number of doses can increased based upon progression or failure to reduce the progression of the cancer, increased severity or no change in severity of the cancer symptoms, increased frequency or no change in the frequency of the cancer symptoms, increased size or no change in size of the tumor, or any combination thereof. For example, the subject can be administered 1 to 100 doses or more of the composition. [00325] Factors that can determine the dose of the host cell include, for example, the progression of the cancer, the severity of the cancer symptoms, the frequency of the cancer symptoms, tumor size, or any combination thereof. In some embodiments, the composition can comprise about 1 x 10 ⁸ to about 1 x 10 ⁹ colony forming units (CFU) of a host cell. In some aspects, the composition can comprise about 1 x 10 ⁸ CFU of a host cell. In some aspects, the composition can comprise about 1 x 10 ⁹ CFU of a host cell.

[00326] The composition can be administered about once every 7 days, about once about every 14 days, about once every 21 days, about once every 28 days, about once every 35 days, about once every 42 days, about once every 49 days, about once every 56 days, about once every 63 days, about once every 70 days, about once every 77 days, about once every 84 days, or about once every 91 days.

[00327] Based on the forgoing, those skilled in the art would understand that a subject could be treated for the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof by administering a described dose of any one of the compositions descried herein, where the dosing is repeated at a regular interval as described. Accordingly, in one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁸ to about 1 x 10 ⁹ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 7 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁸ to about 1 x 10 ⁹ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 14 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁸ to about 1 x 10 ⁹ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 21 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁸ to about 1 x 10 ⁹ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 35 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁸ to about 1 x 10 ⁹ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 45 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁸ to about 1 x 10 ⁹ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 60 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁸ to about 1 x 10 ⁹ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 90 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁸ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 7 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁸ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 14 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁸ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 21 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁸ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 35 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁸ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 45 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁸ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 60 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁸ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 90 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁹ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 7 days Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁹ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 14 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁹ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 21 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁹ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 35 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁹ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 45 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁹ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 60 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner. In one embodiment a composition may be administered to a subject at a dose of about 1 x 10 ⁹ CFU to treat the progression of cancer, the severity of cancer symptoms, the frequency of cancer symptoms, tumor size, or any combination thereof, where the dosing is repeated about once every 90 days. Furthermore, the compositions described herein could be prepared in a pharmaceutical preparation suitable for such a dose to be administered in this manner.

[00328] Preferably, treatment can include a period of time between doses wherein the composition is not administered to the subject. For example, the methods can comprise administering to the subject a first dose of a composition comprising a host cell, wherein the host cell comprises a nucleic acid molecule encoding an immunogenic fusion protein, monitoring the efficacy of the first dose, and, if the first dose is not efficacious, administering to the subject one or more doses of the composition. Factors that can determine the efficacy of the composition include, for example, the progression of the cancer, the severity of the cancer symptoms, the frequency of the cancer symptoms, tumor size, or any combination thereof. Without intent to be limiting, progression or failure to reduce the progression of the cancer, increased severity or no change in severity of the cancer symptoms, increased - I l l - frequency or no change in the frequency of the cancer symptoms, increased size or no change in size of the tumor, or any combination thereof, can be indications that the first dose of the composition is not efficacious. Suitable periods of time between doses include days, weeks, or months. In some embodiments, the period of time between doses can be about 1 day to about 90 days, about 5 days to about 80 days, about 10 days to about 70 days, about 15 days to about 60 days, about 20 days to about 50 days, or about 25 days to about 40 days. For example, the period between doses can be about 1 day, about 2 days, about 3 days, about 4 days, about 5 days, about 6 days, about 7 days, about 14 days, about 21 days, about 28 days, about 35 days, about 42 days, about 49 days, about 56 days, about 60 days, about 65 days, about 70 days, about 80 days, about 85 days, or about 90 days.

[00329] Suitable modes of administering the composition to the subject include, but are not limited to, intravenously, orally, subcutaneously, intradermally, intramuscularly, intraperitoneally, transmucosally, nasal administration, or any combination thereof. In some embodiments, the administering step can be performed intravenously.

[00330] Treatment can further comprise administering an antibiotic to the subject after administering the composition. For example, once the final dose of the composition is administered to the patient, and after a suitable interval time, the patient can be given an antibiotic. Thus, in a preferred aspect, the antibiotic is administered after a last dose of the composition. Suitable antibiotics include, but are not limited to, amoxicillin or

trimethoprim/sulfamethoxazole in subjects who are allergic to penicillin. One skilled in the art would be able to determine a sufficient dosing and dosing schedule for administering the antibiotic to the subject.

[00331] The following examples are provided to further describe some of the

embodiments disclosed herein. The examples are intended to illustrate, not to limit, the disclosed embodiments.

[00332] EXAMPLES

[00333] Methods

[00334] Molecular construction of vaccine strains

[00335] All vaccine strains were constructed in the Listeria monocytogenes AactA AinlB strain background as described in Brockstedt, D.G., et al., Listeria-based cancer vaccines that segregate immunogenicity from toxicity. PNAS (2004) 101(38): 13832-13837, which is incorporated herein in its entirety. The EGFRvIII, SSX2, PAP, KX3.1, and PSMA open reading frames were codon optimized using Listeria monocytogenes codon bias, and then the fragments described in Table 1 were PCR amplified and cloned under control of the actA promoter and operably linked with the modified ActANlOO* sequence as disclosed in Int'l Publ. No. WO2014/106123; U.S. Publ. No. 2014/186387, which is hereby incorporated by reference. Antigen expression cassettes were inserted at the actA or MB locus by allelic exchange as described in Camilli, A. et al, Dual roles of plcA in Listeria monocytogenes pathogenesis. Molecular Microbiology (1993) 8(1): 143-157, which is incorporated herein in its entirety. Allelic exchange vectors were assembled by cloning approximately 1 kilobase of DNA sequence from either side of the deleted actA or inlB into a derivative of pKSV7. The antigen expression cassette was cloned into the pKSV7 vector between the actA or MB flanking homology.

[00336] A single expression cassette was cloned into the actA allelic exchange vector that comprised of the actA promoter, the ActANlOO* coding sequence, the 5 copies of the 21 amino acid EGFRvIII junction region, and the codon optimized full-length SSX2 sequence, and was used to construct strains BH5258 and BH5290. Similarly, two expression cassettes were cloned into the MB allelic exchange vector: the first included the actA promoter, the ActANlOO* coding sequence, the 5 copies of the 21 amino acid EGFRvIII junction region, and the codon optimized PAP encoding amino acids 33-386 (used to construct BH5258 and BH5290); the second included the actA promoter, the ActANlOO* coding sequence, the full- length codon-optimized NKX3.1 sequence, and the codon optimized PAP encoding amino acids 33-386 (used to construct strains BH4598 and BH4602). Allelic exchange was performed as described previously in Camilli, A. et al, Dual roles of plcA in Listeria monocytogenes pathogenesis. Molecular Microbiology (1993) 8(1): 143-157.

[00337] For antigen expression cassettes inserted at the tRNA ^Avg locus, site specific recombination was used to stably integrate the constructs on the Lm chromosome. Antigen expression cassettes were cloned into a derivative of the pPL2 integration vector as described in Lauer et al., Infect. Immun. (2008) 76: 3742-53, which is incorporated herein in its entirety, that had been modified to allow removal of extraneous vector sequences including all antibiotic resistance markers as described in Int'l Publ. No. WO2007/103225; U.S. App. No. PCT/US2007/005457, which is hereby incorporated by reference. The expression cassette including the actA promoter, the ActANlOO* coding sequence, the 5 copies of EGFRvIII junctional region, the codon optimized sequences for NKX3.1 spanning amino acids 11-243, and PSMA spanning amino acids 1-20, 44-138, and 169-750 were cloned and integrated at the tRNA ^Avg locus. Two variant strains differed in a single encoded amino acid in the KX3.1 coding sequence at amino acid 41 : BH5258 encodes arginine at amino acid 41; and BH5290 encodes glycine at amino acid 41. Transient FLP recombinase expression from a temperature sensitive plasmid was used for removal of the plasmid backbone and antibiotic resistance markers. All final antigen expression cassettes were confirmed by DNA sequencing.

[00338] Intracellular western blots

[00339] The mouse dendritic cell line DC2.4 was inoculated with Listeria monocytogenes strains at a multiplicity of infection (MO I) of 10 for 1 hour, the cells were washed 3 x with PBS and DMEM media supplemented with 50 μg/mL gentamycin. Cells were harvested at 7 hours post infection. Cells were lysed with SDS sample buffer, collected and run on 4-12% polyacrylamide gels and transferred to nitrocellulose membranes for western blot analysis. Antigen detection was visualized and quantitated with the Licor Odyssey IR detection system using a polyclonal antibody raised against the mature N-terminus of the ActA protein and were normalized to p60 expression (an unrelated Lm protein) with an anti-p60 monoclonal antibody. P60 levels correlate directly with the number of bacteria in the experiment.

[00340] Antigen-specific immune responses in vaccinated mice

[00341] 6 week old Balb/c mice (n=5) were vaccinated intravenously (IV) with 5xl0 ⁶ cfu. After seven days, spleens were harvested and immune responses measured by IFNyELIspot assay using an overlapping peptide libraries for SSX2, PAP, NKX3.1, or PSMA (15mer peptides overlapping by 11 amino acids) or unstimulated media control. For EGFRvIII- specific immunogenicity, 6 week old C3H/HeN mice (n=5) were vaccinated with 5xl0 ⁶ cfu IV. After seven days, spleens were harvested and immune responses measured by IFNy ELIspot assay using the EGFRVIII26-33 - the K ^k binding peptide EEKKGNYV. Data for each strain/antigen are plotted with the unstimulated responses or as background (unstimulated) subtracted data. Statistical significance was determined using the unpaired T-test.

[00342] Protective immunity to a wild-type Listeria challenge

[00343] Balb/c mice were vaccinated once with 2xl0 ⁶ cfu of each Lm strain IV. Forty days later, mice were challenged IV with 5xl0 ⁴ cfu (2x LD ₅₀ dose) of the WT Lm strain DP- L4056 as described in Lauer, 2002. Three days later, spleens were harvested and

homogenized. Dilutions were plated on BHI plates containing 200 μg/mL streptomycin to determine cfu/organ. The limit of detection (LOD) in this assay was 50 CFU.

[00344] Treatment of cancer [00345] A first in human (FIH), Phase 1, open-label, multicenter, 2-part study is conducted to characterize the safety, determine a Phase 2 does (RP2D), evaluate the preliminary clinical efficacy, and determine the immune responses of single-agent ADU-741 (also referred to as strain BH5290), when administered to subjects with metastatic castration resistant prostate cancer. Subjects must have disease that has not responded to hormonal therapy and that is progressing at screening, and have received at least 2 prior approved therapies.

Approximately 42 subjects will be enrolled in the study.

[00346] Part 1 (Dose Escalation): is designed to determine the RP2D based on safety and pharmacodynamic assessments. Two doses of ADU-741 (Dose Cohort 1A: lxlO ⁸ CFU and Dose Cohort IB: lxlO ⁹ CFU) are administered sequentially. The total number of subjects enrolled will depend on when and/or whether dose-limiting toxicity is observed.

[00347] Part 2 (Dose Expansion): is designed to evaluate 2 expansion cohorts (Cohort 2A and 2B) after the RP2D for ADU-741 is determined. The goal of the expansion cohorts is to further evaluate the safety of ADU-741 (Cohort 2 A) and to evaluate pre- and posttreatment biopsies for immune response at the tumor site (Cohort 2B).

[00348] Once a subject is determined to be eligible for the study, ADU-741 is administered intravenously every 21 days during the open-label treatment period. ADU-741 is

administered via peripheral vein catheter. The study drug is administered over a 1-hour period with the option to increase the duration of the infusion, if necessary. Subjects are closely monitored for adverse events, laboratory abnormalities, and clinical and immunologic response. Treatment is administered until confirmed radiographic disease progression, unacceptable toxicity, withdrawal of consent, the investigator decides to stop treatment, the start of subsequent anticancer therapy, or the sponsor ends the study. Safety and efficacy is evaluated.

[00349] Study population - Subjects who are over 18 years of age with histologically confirmed adenocarcinoma of the prostate with castration-resistant metastatic disease who have received at least 2 prior approved therapies and have at least 1 of the following criteria for disease progression are eligible for the study: (1) rise in prostate specific antigen (PSA) with a minimum of 3 rising levels, with an interval of >1 week between each determination (the last determination must have a value >2 ng/ml, obtained within 2 weeks prior to enrollment); (2) measurable disease defined as new or progressive soft tissue disease on computed tomography (CT) or magnetic resonance imaging (MRI) scans; (3) radionuclide bone scan or 18F sodium fluoride positron emission tomography/computed tomography (NaF PET/CT) result with at least 2 new bone lesions, as determined by the Prostate Cancer Clinical Trials Working Group (PCWG2) criteria; and must have received at least 2 prior approved therapies. Subjects must have an Eastern Cooperative Oncology Group (ECOG) Performance status score of 0 or 1.

[00350] Efficacy Evaluations - Efficacy assessments are evaluated by the investigator according to the PCWG2 criteria, Response Evaluation Criteria in Solid Tumors (VI .1) (RECIST) criteria, and Immune-Related Response Criteria (irRC). Disease response is assessed using CT scans with IV contrast of the chest, abdomen, and pelvis. Subjects who are intolerant of IV CT contrast agents have CT scans performed with oral contrast. Magnetic resonance imaging (MRI) may be used to evaluate sites of disease that cannot be adequately imaged using CT. Soft tissue disease (ie, radiologically detectable tumors) is assessed by CT and/or MRI. Radionuclide bone scans or 18F-NaF PET/CT is performed to evaluate site of bone disease. These assessments are performed throughout the study at each timepoint using the same method of assessment used to assess disease at baseline. Data also is collected on subsequent anti-cancer therapies and overall survival in the posttreatment follow-up period.

[00351] Results

[00352] KX3.1 (R41G) results in higher expression of all encoded antigens

[00353] Two multivalent vaccine strains BH5258 (containing "wild type" KX3.1) and BH5290 (with the KX3.1 R41G variation) differ by a single amino acid at position 41 of KX3.1. Strains were constructed that express the five encoded antigens from three loci in the Lm genome as described (FIG. 1). These strains were used to infect the mouse dendritic cell line DC2.4, and expression was measured using semi -quantitative western blots. Each of the fusion proteins were detected at approximately the predicted sizes. Surprisingly, for each encoded fusion protein antigen (PSMA, PAP, KX3.1, SSX2, and EGFRvIII), expression ranged from 2. lx-3.2x higher in the strains that contained the KX3.1 (R41 G) variation, indicating a single amino acid change in KX3.1 enhances expression of all encoded antigens. Specifically, KX3.1 and PSMA were 2.7x higher in BH5290, PAP was 3.2x higher expression in BH5290, SSX2 was 2. lx higher in BH5290, and EGFRvIII was 2. lx- 3.2x higher in BH5290.

[00354] KX3.1 (R41G) results in higher antigen-specific immunogenicity

[00355] The two multivalent vaccine strains BH5258 and BH5290 were compared for T cell immunogenicity in mice (FIG. 3). Immune responses to SSX2, PAP, KX3.1, and PSMA were measured in Balb/c mice. EGFRvIII were measured in C3H/HeN mice. Responses to 4 of 5 encoded antigens were higher in BH5290, with the single amino acid difference in the KX3.1 coding sequence ( KX3.1(R41G)). Responses to PAP were statistically higher in BH5290 compared to BH5258. PSMA responses were essentially equivalent with both strains. The single amino acid difference between BH5290 and BH5258 resulted in higher immune responses to most of the encoded antigens, indicating that it is the more potent prostate cancer vaccine.

[00356] BH5290 induces fully functional and protective immunity when challenged with a WT Lm

[00357] As shown in FIG. 4, a single vaccination with BH5290 induces fully protective, long-term immunity to a WT Listeria challenge. Vaccination with BH5290 resulted in a 5- log reduction in CFU in the spleen after WT-Lm challenge. Functional immunity is a combination of magnitude of the antigen-specific immune response and the ability of the immune response to protect from a future challenge. In this case, the functionality was tested with a fully virulent wild-type Listeria challenge. Vaccination with HBSS or the Lm strain DP-L4027 (hly-) were included in the experiment as negative controls.

[00358] SSX2 expression is increased when EGFRvIIIx5 is included as a part of the fusion protein

[00359] To assess the impact of inclusion of EGFRvIIIx5 on antigen expression, matched SSX2 expression cassettes differing only in the presence of EGFRvIIIx5, were introduced at the tRNA ^Arg locus of the same Lm background that expressed an ActAN100*- KX3.1-PAP _{33- 38} 6 fusion protein from the inlB locus. BH4598 contained the first cassette - ActANlOO*- SSX2, and BH4602 contained the second cassette - ActAN100*-EGFRvIIIx5-SSX2 (FIG. 5A). All expression cassettes utilized the actA promoter. Expression of these cassettes was then assessed by intracellular western blot (FIG. 5B). Lane 1 : Lml 1 (negative control), lane 2: BH4598 (ActAN100*-SSX2), lane 3 : BH4602 (ActAN100*-EGFRvIIIx5-SSX2). Full- length sized bands for each of the fusion proteins are indicated on the right. Expression levels were quantified and data was normalized to the constitutive Listeria P60 protein. The relative expression level of the constant expression cassette (the KX3.1-PAP fusion) was similar between the two strains (0.43 in BH4598 and 0.33 in BH4602). However, the expression of the SSX2 fusion protein was over 200-fold higher in the strain that contained EGFRvIIIx5 as part of the fusion (1 in BH4598 and 224 in BH4602). This data clearly demonstrate that EGFRvIIIx5 augments expression of SSX2. [00360] SSX2 immune responses are significantly higher when EGFRvIIIx5 is part of the immunogenic fusion protein

[00361] Primary immune responses induced by BH4598 and BH4602 were compared. BH4602 induced significantly higher SSX2-specific immune responses than BH4598 (p=0.0024). This demonstrates that the higher expression from the the EGFRvIII-SSX2 fusion protein translated to higher immune responses in mouse models of immunogenicity.

[00362] PAP expression is higher when fused to multiple copies of EGFRvIII

[00363] As shown in FIG. 7, each additional EGFRvIII repeat unit resulted in higher expression of PAP. Relative expression measured in lanes 2-7: lx, 2.4x, 19.6x, 127x, 156x, and 213x, respectively. Additionally, the increase in expression for fusion of EGFRvIIIx5 to both SSX2 and PAP resulted in an increase in expression over 200x for both antigens.

[00364] PAP responses are higher when fused to multiple copies of EGFRvIII and are significantly higher when fused to 5 copies of EGFRvIII

[00365] Six PAP expressing Lm strains with the variation in EGFRvIII copy number (BH2868, PL1631, PL1629, PL1627, PL1625, and PL1623) were tested for induction of T cell responses. BH2868 (zero copies of EGFRvIII) induced low but detectable PAP-specific immune responses. All strains that included at least one copy of EGFRvIII as part of the PAP fusion induced higher PAP-specific immune responses, and there was a trend in the immune responses that mirrored the increase in expression level - more copies of EGFRvIII resulted in higher immune responses. The highest immune responses were observed from PL1623 (five copies of EGFRvIII), and the response was statistically higher than strains with no EGFRvIII or one copy of the EGFRvIII repeat. Likewise, PL 1629 with two copies of the repeat induced significantly higher PAP responses than the strain with zero copies of EGFRvIII.

[00366] Those skilled in the art will appreciate that numerous changes and modifications can be made to the preferred embodiments of the invention and that such changes and modifications can be made without departing from the spirit of the invention. It is, therefore, intended that the appended claims cover all such equivalent variations as fall within the true spirit and scope of the invention.

[00367] The disclosures of each patent, patent application, and publication cited or described in this document are hereby incorporated herein by reference, in its entirety.

Table 5

. h i. I X HHI * inicl coli dc sequence ( S I X) I I ) \( ) 1 )

gcaagcaaagtattgccagctagtcgtgcattagaggagaaaaaggggaattacgtggtg acggatcatggatcgtgtgccgatggctc SRASLVS VYNSYPYYPYLYC YGS\VSFAF\VtsMWNLLHETDSA VA TARRPR WKSSNEA T NITPKHNMKAFLDELKAENIKKFLYNFTQIPHLAGTEQNFQLAKQIQSQWKEFGLDSVEL A HYD VLLSYPNKTHPNYISIINEDGNEIqlMPEGDL VYVNYARTEDFFKLERDMKINCSGKIVIA R YGKVFRGNKVKNA QLA GAKG VIL YSDPAD YFAPG VKSYPDG WNLPGGG VQRGNILNLNG A GDPL TPGYPANEYA YRRGIAEA VGLPSIP VHPIGYYDA QKLLEKMGGSAPPDSSWRGSLKV PYNVGPGFTGNFSTQKVKMHIHSTNEVTRIYNVIGTLRGA VEPDRYVILGGHRDSWVFGGI DPQSGAA WHEIVRSFGTLKKEGWRPRRTILFASWDAEEFGLLGSTEWAEENSRLLQERGV A YINADSSIEGNYTLR VDC TPLMYSL VHNL TKELKSPDEGFEGKSL YESWTKKSPSPEFSGM PRISKLGSGNDFEVFFQRLGIASGRARYTKNWETNKFSGYPLYHSVYETYELVEKFYDPM FK YHL TV A Q VRGGMVFELANSIVLPFDCRDYA WLRKYADKIYSISMKHPQEMKTYSVSFDSLF SA VKNFTEIASKFSERLQDFDKSNPIVLRMMNDQLMFLERAFIDPLGLPDRPFYRHVIYAPS SHNKYAGESFPGIYDALFDIESKVDPSKA WGEVKRQIYVAAFTVQAAAETLSEVA

.ΧΚ.Χλ /fR-f /G) : - . nucl eoti de sequence ( S I X,) I I ) NO 1 7 ) gaagcaaaagctgaaggcgcagcgccaccgactcctagtaaaccactaacaagtttctta atccaagatattcttcgtgacggtgcacaa ggacaaggcggacgaacttcttcacaacgtcaacgagatcctgagccagaaccggagcct gaaccggaagggggacgctcccgag ctggagcacaaaacgatcagttatctactggtccaagagctgcccctgaagaagcagaga cactagccgaaacggaaccagaaagac atttgggttcatacttacttgactcagaaaacacaagcggggctttaccgagattaccac aaacaccaaaacagcctcaaaaacgtagtc gtgctgcattttcgcacacgcaagtcatagagttagaacgcaaattcagccatcaaaagt atttgtccgcaccagaacgtgctcatcttgcg aagaatttgaaacttacagaaacccaagtaaagatttggtttcaaaatcgccgctataag acgaaacgtaaacaactttcttctgaactagg tgatttagaaaaacattcaagccttccggcgttaaaggaagaagcatttagtcgtgcgag cttagtttctgtttacaatagttatccatactatc catatctatactgtgtaggctcgtggtcgccagctttttgg

\ k .\ l ( 4 1 ( i ) i | . - ; | ami no aci d sequence ( S l - O I D \() I S )

EAKAEGAAPPTPSKPLTSFLIQDILRDGAQGQGGRTSSQRQRDPEPEPEPEPEGGR

SRAGAQNDQLSTGPRAAPEEAETLAETEPERHLGSYLLDSENTSGALPRLPQTPK

QPQKRSRAAFSHTQVIELERKFSHQKYLSAPERAHLAKNLKLTETQVKIWFQNR

RYKTKRKQLSSELGDLEKHSSLPALKEEAFSRASLVSVYNSYPYYPYLYCVGSWS

PAFW

/ '.S ^' \ /. I . ·,, -,, nucl eoli cle sequence I I ) \( ) < ^■) )

( M l ^' cl l i n ker dolled u nderl i ned )

atgtggaacttattacacgaaacagactcagcagtagcaacagccagacgccctcgt tggaaatcaagcaacgaagctaccaatatcac cccgaaacacaatatgaaagcattcctagacgaactaaaagcagaaaacataaaaaaatt tctttacaatttcacacagattccacatttag ctggtacggagcaaaactttcaattagcaaaacaaattcaatctcaatggaaagaatttg gtttagacagtgtagaattggctcattacgatg tccttttatcttatccgaataaaacgcatccaaattacatttcaattattaatgaagatg gaaatgaaatacaattgatgcctgagggcgattta gtgtatgttaactatgcgcgcacagaggatttctttaaacttgaacgggatatgaaaatc aactgttctggtaaaatcgtcattgctcgttatg gcaaagtatttcgtggcaacaaagtaaagaatgcacaattagcgggtgcgaaaggcgtca tattatactccgatccagcagattactttgc acctggagtaaaatcctatccagatggctggaatttgccaggtgggggtgtacagcgtgg caatattcttaatcttaatggggctggtgac cctttaactcctggttatccagctaatgaatacgcttatcgtcgtggaatcgcagaagcc gtgggactaccctcaattcctgtacatccaatc ggatactatgatgctcaaaaattattagaaaagatgggggggtccgctccaccagattcg agctggcgtggaagtctcaaagttccatac aatgtaggcccgggttttactggcaacttttcaacacaaaaagtgaaaatgcacattcat tccacgaatgaagtgactcgaatatacaatgt cattggaactctccgtggtgcggttgagccagacagatatgtaatccttggcggacaccg agatagttgggtatttggaggtattgatcca caaagtggagcagcggttgttcatgaaattgttagaagtttcggtacacttaagaaagaa gggtggcgaccacgccgtacgattttgtttg cttcgtgggatgccgaagagttcggacttttgggatctacagaatgggcagaagagaaca gccgtttattgcaagaacgcggggtagct tatattaatgctgatagtagtattgaaggtaactatacattaagagtggactgtacgccg ttaatgtattcgctagtccataaccttacaaaag aacttaaaagcccagatgaagggttcgaagggaaatcgctttatgaatcatggacaaaga aatctccatcaccagagttctctggaatgc ctcgtatcagtaaattgggtagcggaaacgactttgaagttttctttcaacgtctaggca ttgcgtcggggagagcgcggtacaccaaaaa ctgggaaaccaataagtttagcggctatccactctatcattctgtgtatgaaacatacga gcttgtagaaaaattttatgatccgatgtttaaat atcatcttacagttgctcaggtccggggtggaatggtttttgagttggctaattccattg tacttccatttgactgccgcgattacgctgtggtg ctaagaaaatacgctgataaaatctattccatttcaatgaaacacccacaagaaatgaaa acttatagcgtgagttttgatagtttattcagtg ccgtaaagaactttactgaaatcgccagcaagttttctgaaagattacaagatttcgata aatctaatcctatagtattaagaatgatgaatga tcaactaatgtttttagaacgagcgttcattgatccgttaggtttaccggatcgaccttt ctatcgtcacgttatctacgctcccagtagccata acaaatatgcaggcgaatcttttccaggaatctatgacgccctattcgatatagaaagta aagttgatccgagtaaagcatggggtgaagtt aaacgacaaatctatgtcgcggcattcactgttcaagcagcggctgaaactttatcagaa gttgct

PS\ I \ | ..„ | |. | : _S i,,.).--.. ami no aci d se ue ce ( S I - („) I I ) \( ) 2< > )

( M l ^' cl l i n ker μΙ dolled underl i ned )

MW LLHETDSAVATARRPRWKSS EATNITPKHNMKAFLDELKAENIKKFLY FTQI

PHLAGTEQ FQLAKQIQSQWKEFGLDSVELAHYDVLLSYP KTHPNYISIINEDG EIql

MPEGDLVYVNYARTEDFFKLERDMKINCSGKIVIARYGKVFRG KVKNAQLAGAKG

VILYSDPADYFAPGVKSYPDGW LPGGGVQRGNIL LNGAGDPLTPGYPANEYAYRR

GI AEA VGLP SIPVHPIGYYD AQKLLEKMGGS APPD S SWRGSLK VP YNVGPGFTG F ST

QKVKMHIHST EVTRIYNVIGTLRGAVEPDRYVILGGHRDSWVFGGIDPQSGAAVVH

EIVRSFGTLKKEGWRPRRTILFASWDAEEFGLLGSTEWAEENSRLLQERGVAYINAD S

SIEGNYTLRVDCTPLMYSLVHNLTKELKSPDEGFEGKSLYESWTKKSPSPEFSGMPR IS

KLGSG DFEVFFQRLGIASGRARYTKNWETNKFSGYPLYHSVYETYELVEKFYDPMF

KYHLTVAQVRGGMVFELANSIVLPFDCRDYAVVLRKYADKIYSISMKHPQEMKTYSV

SFDSLFSAVK FTEIASKFSERLQDFDKS PIVLRMMNDQLMFLERAFIDPLGLPDRPF

YRHVIYAPSSHNKYAGESFPGIYDALFDIESKVDPSKAWGEVKRQIYVAAFTVQAAA E

TLSEVA

gggaagcagttggggttaactgattaacaaatgttagagaaaaattaattctccaagtga tattcttaaaataattcatgaatattttttcttatat tagctaattaagaagataattaactgctaatccaatttttaacggaataaattagtgaaa atgaaggccgaattttccttgttctaaaaaggttg tattagcgtatcacgaggagggagtataagtgggattaaatagatttatgcgtgcgatga tggtagttttcattactgccaactgcattacga ttaaccccgacataatatttgcagcgacagatagcgaagattccagtctaaacacagatg aatgggaagaagaatacgaaactgcacgt gaagtaagttcacgtgatattgaggaactagaaaaatcgaataaagtgaaaaatacgaac aaagcagaccaagataataaacgtaaagc aaaagcagagaaaggtggatctgcaagcaaagtattgccagctagtcgtgcattagagga gaaaaaggggaattacgtggtgacggat catggatcgtgtgccgatggctcagtaaagactagcgcgagcaaagtggcccctgcatca cgagcacttgaagagaaaaaaggaaac tatgttgtgaccgatcatggtagctgcggagatggttcaattaaattatcaaaagtctta ccagcatctagagctttagaggaaaagaaggg taactatgtcgtaacagatcatggaagttgtgctgacggaagtgttaaagcgtcgaaagt agctccagcttctcgcgcattagaagaaaag aaaggcaattatgttgtaacagaccatggtagttgtggtgatggctcgatcaaattgtca aaagttctaccggcttctcgtgcgctagaaga gaagaaaggaaattacgtagttacagaccacggctcttgcgcggatggttccgttaaagg atccgaagcaaaagctgaaggcgcagcg ccaccgactcctagtaaaccactaacaagtttcttaatccaagatattcttcgtgacggt gcacaaagacaaggcggacgaacttcttcac aacgtcaacgagatcctgagccagaaccggagcctgaaccggaagggggacgctcccgag ctggagcacaaaacgatcagttatct actggtccaagagctgcccctgaagaagcagagacactagccgaaacggaaccagaaaga catttgggttcatacttacttgactcaga aaacacaagcggggctttaccgagattaccacaaacaccaaaacagcctcaaaaacgtag tcgtgctgcattttcgcacacgcaagtca tagagttagaacgcaaattcagccatcaaaagtatttgtccgcaccagaacgtgctcatc ttgcgaagaatttgaaacttacagaaaccca agtaaagatttggtttcaaaatcgccgctataagacgaaacgtaaacaactttcttctga actaggtgatttagaaaaacattcaagccttcc ggcgttaaaggaagaagcatttagtcgtgcgagcttagtttctgtttacaatagttatcc atactatccatatctatactgtgtaggctcgtggt cgccagctttttggactagtatgtggaacttattacacgaaacagactcagcagtagcaa cagccagacgccctcgttggaaatcaagca acgaagctaccaatatcaccccgaaacacaatatgaaagcattcctagacgaactaaaag cagaaaacataaaaaaatttctttacaattt cacacagattccacatttagctggtacggagcaaaactttcaattagcaaaacaaattca atctcaatggaaagaatttggtttagacagtgt agaattggctcattacgatgtccttttatcttatccgaataaaacgcatccaaattacat ttcaattattaatgaagatggaaatgaaatacaatt gatgcctgagggcgatttagtgtatgttaactatgcgcgcacagaggatttctttaaact tgaacgggatatgaaaatcaactgttctggtaa

a ggg caac ac gaccagaaaacacaagcggggc accgaga accacaaacaccaaaacagcccaaaaacgagc GCGACAGATAGCGAAGATTCCAGTCTAAACACAGATGAATGGGAAGAAGAAAAA ACAGAAGAGCAGCCAAGCGAGGTAAATACGGGACCAAGATACGAAACTGCACGT GAAGTAAGTTCACGTGATATTGAGGAACTAGAAAAATCGAATAAAGTGAAAAAT ACGAACAAAGCAGACCTAATAGCAATGTTGAAAGCAAAAGCAGAGAAAGGTggatc cGTATTGGCAAAAGAACTAAAGTTTGTAACGTTAGTCTTTAGACATGGTGATC GTAGTCCTATTGATACCTTTCCTACAGATCCAATCAAAGAGAGTAGTTGGCCA CAAGGCTTCGGACAACTTACACAATTAGGAATGGAACAACATTATGAATTAG GTGAATACATTCGCAAACGTTATCGCAAATTCCTTAATGAATCGTACAAACAC GAACAAGTGTATATCCGTTCCACTGACGTTGATAGAACACTAATGTCAGCTAT GACAAATCTAGCTGCATTAGTGCCACCAGAAGGCGTTAGCATTTGGAATCCT ATCTTACTTTGGCAGCCAATACCTGTACATACGGTTCCGTTATCTGAAGATCA ATTACTTTATCTTCCATTTCGCAACTGCCCACGATTCCAAGAATTAGAATCCG AAACATTGAAAAGCGAAGAATTTCAGAAAAGATTACATCCATACAAAGACTTT ATCGCAACCTTAGGCAAATTGTCAGGGTTACACGGACAGGATCTATTTGGAA TTTGGTCGAAAGTTTATGATCCTTTGTACTGTGAATCTGTACATAACTTTACA TTACCTAGTCGCGCCACGGAAGATACTATGACGAAACTACGTGAACTTTCCG AACTTTCTTTACTATCGTTGTATGGTATTCATAAACAAAAAGAAAAGAGCAGA TTGCAAGGTGGTGTTTTAGTAAATGAAATCTTAAACCATATGAAAAGAGCTAC ACAAATTCCGTCTTACAAGAAATTGATTATGTATAGTGCTCATGATACGACAG TATCTGGGCTTCAAATGGCGTTAGATGTCTATAACGGCTTACTTCCACCGTAT GCGTCATGTCACCTTACGGAACTTTACTTTGAGAAAGGTGAGTACTTTGTTGA GATGTACTATCGCAATGAAACCCAACATGAACCATATCCGTTGATGTTACCAG GTTGTAGTCCATCTTGCCCGTTAGAACGATTTGCGGAATTAGTGGGTCCAGT GATACCACAAGACTGGTCTACTGAGTGTATGACTACTAATAGCCACCAAGGG ACTGAAGATTCAACAGATactagtcaattgggtgacggtagtattaaacttagcaaagta ttacaattagaaagtattatt aattttgaaaaattagctgatggttcagttaaataa

\ct W I < )( ;x,,-Sl .S ami no aci d sequence ( S I X.) I D \()

gill mm: 1111

MGL RFMRAMMVVFITANCITINPDIIFAATDSEDSSLNTDEWEEEKTEEQPSEVNTGP

RYETAREVSSRDIEELEKS KVKNT KADLIAMLKAKAEKGGSVLAKELKFVTLVF

RHGDRSPIDTFPTDPIKESSWPQGFGQLTQLGMEQHYELGEYIRKRYRKFLNESY

KHEQVYIRSTDVDRTLMSAMTNLAALVPPEGVSIWNPILLWQPIPVHTVPLSEDQ

LLYLPFRNCPRFQELESETLKSEEFQKRLHPYKDFIATLGKLSGLHGQDLFGIWS

KVYDPLYCESVHNFTLPSRATEDTMTKLRELSELSLLSLYGIHKQKEKSRLQGGV

LVNEILNHMKRATQIPSYKKLIMYSAHDTTVSGLQMALDVYNGLLPPYASCHLT

ELYFEKGEYFVEMYYRNETQHEPYPLMLPGCSPSCPLERFAELVGPVIPQDWSTE

CMTTNSHQGTEDSTDTSQLGDGSIKLSKVLQLESIINFEKLADGSVK

clAp-AclAN ^' lOO*-K l' ^' RvIIIx 1-PAP jj.. nucleotide sequence (SEQ ID NO:34) gggaagcagttggggttaactgattaacaaatgttagagaaaaattaattctccaagtga tattcttaaaataattcatgaatattttttcttatat tagctaattaagaagataattaactgctaatccaatttttaacggaataaattagtgaaa atgaaggccgaattttccttgttctaaaaaggttg tattagcgtatcacgaggagggagtataaGTGGGATTAAATAGATTTATGCGTGCGATGA TGGTAGT TTTCATTACTGCCAACTGCATTACGATTAACCCCGACATAATATTTGCAGCGACAG ATAGCGAAGATTCCAGTCTAAACACAGATGAATGGGAAGAAGAATACGAAACTG CACGTGAAGTAAGTTCACGTGATATTGAGGAACTAGAAAAATCGAATAAAGTGAA AAATACGAACAAAGCAGACCAAGATAATAAACGTAAAGCAAAAGCAGAGAAAG GT z tctGCAA GCAAA G TA TTGC CAGCTAGTCG TGCA TTA GA GGA GAAAAA GGGGAA TTA CGTGGTGACGGATCATGGATCGTGTGCCGATGGCTCAGTAAAGamtccAAAGAACT AA AGTTTGTAACGTTAGTCTTTAGACATGGTGATCGTAGTCCTATTGATACCTTT CCTACAGATCCAATCAAAGAGAGTAGTTGGCCACAAGGCTTCGGACAACTTA

CACAATTAGGAATGGAACAACATTATGAATTAGGTGAATACATTCGCAAACG

TTATCGCAAATTCCTTAATGAATCGTACAAACACGAACAAGTGTATATCCGTT

CCACTGACGTTGATAGAACACTAATGTCAGCTATGACAAATCTAGCTGCATTA

GTGCCACCAGAAGGCGTTAGCATTTGGAATCCTATCTTACTTTGGCAGCCAA

TACCTGTACATACGGTTCCGTTATCTGAAGATCAATTACTTTATCTTCCATTT

CGCAACTGCCCACGATTCCAAGAATTAGAATCCGAAACATTGAAAAGCGAAG

AATTTCAGAAAAGATTACATCCATACAAAGACTTTATCGCAACCTTAGGCAAA

TTGTCAGGGTTACACGGACAGGATCTATTTGGAATTTGGTCGAAAGTTTATG

ATCCTTTGTACTGTGAATCTGTACATAACTTTACATTACCTAGTCGCGCCACG

GAAGATACTATGACGAAACTACGTGAACTTTCCGAACTTTCTTTACTATCGTT

GTATGGTATTCATAAACAAAAAGAAAAGAGCAGATTGCAAGGTGGTGTTTTA

GTAAATGAAATCTTAAACCATATGAAAAGAGCTACACAAATTCCGTCTTACAA

GAAATTGATTATGTATAGTGCTCATGATACGACAGTATCTGGGCTTCAAATGG

CGTTAGATGTCTATAACGGCTTACTTCCACCGTATGCGTCATGTCACCTTACG

GAACTTTACTTTGAGAAAGGTGAGTACTTTGTTGAGATGTACTATCGCAATGA

AACCCAACATGAACCATATCCGTTGATGTTACCAGGTTGTAGTCCATCTTGCC

CGTTAGAACGATTTGCGGAATTAGTGGGTCCAGTGATACCACAAGACTGGTC

TACTGAGTGTATGACTACTAATAGCCACCAAGGGACTGAAGATTCAACAGATt aa

\ l \ \ 1 1 ⁾ i !*-/·. ⁽ / ^' /· AY///.v /-P \ P -. ;. =s,, am i no acid s qu nc ( SI -!Q I I ) NO 35 )

MGL RFMRAMMV IT ANCITEStPDIIF AATD SED S SLNTDEWEEEYET ARE VS SRDIE ELEKS KVK TOKADQD K KAKAEKGG^

G^ KGSKELKFVTLVFRHGDRSPIDTFPTDPIKESSWPQGFGQLTQLGMEQHYEL

GEYIRKRYRKFLNESYKHEQVYIRSTDVDRTLMSAMTNLAALVPPEGVSIWNPIL

LWQPIPVHTVPLSEDQLLYLPFRNCPRFQELESETLKSEEFQKRLHPYKDFIATLG

KLSGLHGQDLFGIWSKVYDPLYCESVHNFTLPSRATEDTMTKLRELSELSLLSLY

GIHKQKEKSRLQGGVLVNEILNHMKRATQIPSYKKLIMYSAHDTTVSGLQMALD

VYNGLLPPYASCHLTELYFEKGEYFVEMYYRNETQHEPYPLMLPGCSPSCPLERF

AELVGPVIPQDWSTECMTTNSHQGTEDSTD

ααΐΑρ-ΑαΐΑΑ ⁽⁾ 0*-Ε ⁽ .;ΐ· ^' Κν//Ι ^χ 2-ΡΑΡ_.ι <-^6 nucleotide sequence (SEQ ID NO:36) gggaagcagttggggttaactgattaacaaatgttagagaaaaattaattctccaagtga tattcttaaaataattcatgaatattttttcttatat tagctaattaagaagataattaactgctaatccaatttttaacggaataaattagtgaaa atgaaggccgaattttccttgttctaaaaaggttg tattagcgtatcacgaggagggagtataaGTGGGATTAAATAGATTTATGCGTGCGATGA TGGTAGT TTTCATTACTGCCAACTGCATTACGATTAACCCCGACATAATATTTGCAGCGACAG ATAGCGAAGATTCCAGTCTAAACACAGATGAATGGGAAGAAGAATACGAAACTG CACGTGAAGTAAGTTCACGTGATATTGAGGAACTAGAAAAATCGAATAAAGTGAA AAATACGAACAAAGCAGACCAAGATAATAAACGTAAAGCAAAAGCAGAGAAAG GTGGATCTGCA4 GCAAAGTA TTGCCAGC TAGTCGTGCA TTAGA GGA GAAAAAGGGGAA TTACGTGGTGACGGATCATGGATCGTGTGCCGATGGCTCAGTAAAGACTAGCGCGAGC AAAGTGGCCCCTGCATCACGAGCACTTGAAGAGAAAAAAGGAAACTATGTTGTGACCGA TCA TGGTAGCTGCGGAGA TGGTTCAAAA GGATCCAAAGAACTAAAGTTTGTAACGT TAGTCTTTAGACATGGTGATCGTAGTCCTATTGATACCTTTCCTACAGATCCA ATCAAAGAGAGTAGTTGGCCACAAGGCTTCGGACAACTTACACAATTAGGAA TGGAACAACATTATGAATTAGGTGAATACATTCGCAAACGTTATCGCAAATTC CTTAATGAATCGTACAAACACGAACAAGTGTATATCCGTTCCACTGACGTTGA TAGAACACTAATGTCAGCTATGACAAATCTAGCTGCATTAGTGCCACCAGAA GGCGTTAGCATTTGGAATCCTATCTTACTTTGGCAGCCAATACCTGTACATAC GGTTCCGTTATCTGAAGATCAATTACTTTATCTTCCATTTCGCAACTGCCCAC

TCTTTACTATCGTTGTATGGTATTCATAAACAAAAAGAAAAGAGCAGATTGCA

AGGTGGTGTTTTAGTAAATGAAATCTTAAACCATATGAAAAGAGCTACACAAA

TTCCGTCTTACAAGAAATTGATTATGTATAGTGCTCATGATACGACAGTATCT

GGGCTTCAAATGGCGTTAGATGTCTATAACGGCTTACTTCCACCGTATGCGT

CATGTCACCTTACGGAACTTTACTTTGAGAAAGGTGAGTACTTTGTTGAGATG

TACTATCGCAATGAAACCCAACATGAACCATATCCGTTGATGTTACCAGGTTG

TAGTCCATCTTGCCCGTTAGAACGATTTGCGGAATTAGTGGGTCCAGTGATA

CCACAAGACTGGTCTACTGAGTGTATGACTACTAATAGCCACCAAGGGACTG

AAGATTCAACAGATtaa

\ct W 1 1 -/. ⁽ /7 ΑΥ///.ν Ρ \ P -. ;. :S„ am i no acid sequence ( S I !Q I I ) \ ( ) J )

MGL RFMRAMMV IT ANCITEStPDIIF AATD SED S SLNTDEWEEEYET ARE VS SRDIE ELEKS KVK TOKADQD K KAKAEKGG^

GSVKTSASKVAPASRALEEKKGNYWTDHGSCGDGSIKLSKVLPASRALEEKKGNYWTDH

G^C4Z)G^FGSKELKFVTLVFRHGDRSPIDTFPTDPIKESSWPQGFGQLTQLGMEQ

HYELGEYIRKRYRKFLNESYKHEQVYIRSTDVDRTLMSAMTNLAALVPPEGVSI

WNPILLWQPIPVHTVPLSEDQLLYLPFRNCPRFQELESETLKSEEFQKRLHPYKD

FIATLGKLSGLHGQDLFGIWSKVYDPLYCESVHNFTLPSRATEDTMTKLRELSEL

SLLSLYGIHKQKEKSRLQGGVLVNEILNHMKRATQIPSYKKLIMYSAHDTTVSGL

QMALDVYNGLLPPYASCHLTELYFEKGEYFVEMYYRNETQHEPYPLMLPGCSPS

CPLERFAELVGPVIPQDWSTECMTTNSHQGTEDSTD

a lAp-A lAS l ⁽⁾⁽⁾ --l GI Rvlllx-l-l 'AI ' . .- . _^ nucl eoti de sequence ( S I :0 I I ) N O 4< ⁾ ) gggaagcagttggggttaactgattaacaaatgttagagaaaaattaattctccaagtga tattcttaaaataattcatgaatattttttcttatat tagctaattaagaagataattaactgctaatccaatttttaacggaataaattagtgaaa atgaaggccgaattttccttgttctaaaaaggttg tattagcgtatcacgaggagggagtataaGTGGGATTAAATAGATTTATGCGTGCGATGA TGGTAGT

TTTCATTACTGCCAACTGCATTACGATTAACCCCGACATAATATTTGCAGCGACAG

ATAGCGAAGATTCCAGTCTAAACACAGATGAATGGGAAGAAGAATACGAAACTG

CACGTGAAGTAAGTTCACGTGATATTGAGGAACTAGAAAAATCGAATAAAGTGAA

AAATACGAACAAAGCAGACCAAGATAATAAACGTAAAGCAAAAGCAGAGAAAG

GTGGATCTGCA4 GCAAAGTA TTGCCAGC TAGTCGTGCA TTAGA GGA GAAAAAGGGGAA

TTACGTGGTGACGGATCATGGATCGTGTGCCGATGGCTCAGTAAAGACTAGCGCGAG C

AAAGTGGCCCCTGCATCACGAGCACTTGAAGAGAAAAAAGGAAACTATGTTGTGACC GA

TCA TGGTAGCTGCGGAGA TGGTTCAA TTAAA TTA TCAAAAGTCTTACCAGCA TCTAGAGC

TTTAGAGGAAAAGAAGGGTAACTATGTCGTAACAGATCATGGAAGTTGTGCTGACGG AA

GTGTTAAAGCGTCGAAAGTAGCTCCAGCTTCTCGCGCATTAGAAGAAAAGAAAGGCA AT

TA TGTTGTAA CAGACCA TGGTAGTTGTGGTGA TGGC TCGAAA GGATCC AAAGAACT AA

AGTTTGTAACGTTAGTCTTTAGACATGGTGATCGTAGTCCTATTGATACCTTT

CCTACAGATCCAATCAAAGAGAGTAGTTGGCCACAAGGCTTCGGACAACTTA

CACAATTAGGAATGGAACAACATTATGAATTAGGTGAATACATTCGCAAACG

TTATCGCAAATTCCTTAATGAATCGTACAAACACGAACAAGTGTATATCCGTT

CCACTGACGTTGATAGAACACTAATGTCAGCTATGACAAATCTAGCTGCATTA

GTGCCACCAGAAGGCGTTAGCATTTGGAATCCTATCTTACTTTGGCAGCCAA

TACCTGTACATACGGTTCCGTTATCTGAAGATCAATTACTTTATCTTCCATTT

CGCAACTGCCCACGATTCCAAGAATTAGAATCCGAAACATTGAAAAGCGAAG

AATTTCAGAAAAGATTACATCCATACAAAGACTTTATCGCAACCTTAGGCAAA

TTGTCAGGGTTACACGGACAGGATCTATTTGGAATTTGGTCGAAAGTTTATG

ATCCTTTGTACTGTGAATCTGTACATAACTTTACATTACCTAGTCGCGCCACG

GAAGATACTATGACGAAACTACGTGAACTTTCCGAACTTTCTTTACTATCGTT

GTATGGTATTCATAAACAAAAAGAAAAGAGCAGATTGCAAGGTGGTGTTTTA

GTAAATGAAATCTTAAACCATATGAAAAGAGCTACACAAATTCCGTCTTACAA GAAATTGATTATGTATAGTGCTCATGATACGACAGTATCTGGGCTTCAAATGG

CGTTAGATGTCTATAACGGCTTACTTCCACCGTATGCGTCATGTCACCTTACG

GAACTTTACTTTGAGAAAGGTGAGTACTTTGTTGAGATGTACTATCGCAATGA

AACCCAACATGAACCATATCCGTTGATGTTACCAGGTTGTAGTCCATCTTGCC

CGTTAGAACGATTTGCGGAATTAGTGGGTCCAGTGATACCACAAGACTGGTC

TACTGAGTGTATGACTACTAATAGCCACCAAGGGACTGAAGATTCAACAGAT

TAA

\cl \M< ⁾ <> ^::: -/ ^■ ■ ⁽ ;/ ^• R»7//.v-/-P-\P::. _l s„ amino acid sequence (SI!O II) NO 41 )

MGL RFMRAMMV IT ANCITINPDIIF AATD SED S SLNTDEWEEEYET ARE VS SRDIE ELEKS KVK TTSIKADQD KRKAKAEKG^

GSVKTSASKVAPASRALEEKKGNYWTDHGSCGDGSIKLSKVLPASRALEEKKGNYWTDH

GSCADGSVKASKVAPASRALEEKKGNYVVTDHGSCGDGSKGSKE KF\T \FRRGORS

PIDTFPTDPIKESSWPQGFGQLTQLGMEQHYELGEYIRKRYRKFLNESYKHEQVY

IRSTDVDRTLMSAMTNLAALVPPEGVSIWNPILLWQPIPVHTVPLSEDQLLYLPFR

NCPRFQELESETLKSEEFQKRLHPYKDFIATLGKLSGLHGQDLFGIWSKVYDPLY

CESVHNFTLPSRATEDTMTKLRELSELSLLSLYGIHKQKEKSRLQGGVLVNEILN

HMKRATQIPSYKKLIMYSAHDTTVSGLQMALDVYNGLLPPYASCHLTELYFEKG

EYFVEMYYRNETQHEPYPLMLPGCSPSCPLERFAELVGPVIPQDWSTECMTTNS

HQGTEDSTD

EG I Rylll nucleotide se uen e I (Sl-O II) \() 42)

CCAGCTAGTCGTGCATTAGAGGAGAAAAAGGGGAATTACGTGGTGACGGATCATG GATCGTGT

h.GI Rvlll nucleotide sequence 2 (Si :o II) \() 43)

CCTGCATCACGAGCACTTGAAGAGAAAAAAGGAAACTATGTTGTGACCGATCATG GTAGCTGC

h.GI Rvlll n icleolicle sequence (Sl-Q II) NO 44)

G UAftAAGUTlT 1GUT1

CCAGCTTCTCGCGCATTAGAAGAAAAGAAAGGCAATTATGTTGTAACAGACCATG GTAGTTGT

I.GI ^' RvIII nucleotide sequence 5 (Sl-O II) NO 4 )

CCGGCTTCTCGTGCGCTAGAAGAGAAGAAAGGAAATTACGTAGTTACAGACCACG GCTCTTGC

lily promoter nucleotide sequence (SI!O II) NO 47)

tcctttgattagtatattcctatcttaaagttacttttatgtggaggcattaacatt tgttaatgacgtcaaaaggatagcaagactagaataaag ctataaagcaagcatataatattgcgtttcatctttagaagcgaatttcgccaatattat aattatcaaaagagaggggtggcaaacggtattt ggcattattaggttaaaaaatgtagaaggagagtgaaaccc

/ 41 nucleotide sequence (SI O II) N0.4S)

ATGAAAAAAATAATGCTAGTTTTTATTACACTTATATTAGTTAGTCTACCAATTGC

GCAACAAACTGAAGCAAAGGATGCATCTGCATTCAATAAAGAAAATTCAATTTCA

TCCATGGCACCACCAGCATCTCCGCCTGCAAGTCCTAAGACGCCAATCGAAAAGA

AACACGCGGATGAAATCGATAAGTATATACAAGGATTGGATTACAATAAAAACA

ATGTATTAGTATACCACGGAGATGCAGTGACAAATGTGCCGCCAAGAAAAGGTTA

CAAAGATGGAAATGAATATATTGTTGTGGAGAAAAAGAAGAAATCCATCAATCA

AAATAATGCAGACATTCAAGTTGTGAATGCAATTTCGAGCCTAACCTATCCAGGT GCTCTCGTAAAAGCGAATTCGGAATTAGTAGAAAATCAACCAGATGTTCTCCCTG

TAAAACGTGATTCATTAACACTCAGCATTGATTTGCCAGGTATGACTAATCAAGAC

AATAAAATAGTTGTAAAAAATGCCACTAAATCAAACGTTAACAACGCAGTAAATA

CATTAGTGGAAAGATGGAATGAAAAATATGCTCAAGCTTATCCAAATGTAAGTGC

AAAAATTGATTATGATGACGAAATGGCTTACAGTGAATCACAATTAATTGCGAAA

TTTGGTACAGCATTTAAAGCTGTAAATAATAGCTTGAATGTAAACTTCGGCGCAAT

CAGTGAAGGGAAAATGCAAGAAGAAGTCATTAGTTTTAAACAAATTTACTATAAC

GTGAATGTTAATGAACCTACAAGACCTTCCAGATTTTTCGGCAAAGCTGTTACTAA

AGAGCAGTTGCAAGCGCTTGGAGTGAATGCAGAAAATCCTCCTGCATATATCTCA

AGTGTGGCGTATGGCCGTCAAGTTTATTTGAAATTATCAACTAATTCCCATAGTAC

TAAAGTAAAAGCTGCTTTTGATGCTGCCGTAAGCGGAAAATCTGTCTCAGGTGAT

GTAGAACTAACAAATATCATCAAAAATTCTTCCTTCAAAGCCGTAATTTACGGAG

GTTCCGCAAAAGATGAAGTTCAAATCATCGACGGCAACCTCGGAGACTTACGCGA

TATTTTGAAAAAAGGCGCTACTTTTAATCGAGAAACACCAGGAGTTCCCATTGCTT

ATACAACAAACTTCCTAAAAGACAATGAATTAGCTGTTATTAAAAACAACTCAGA

ATATATTGAAACAACTTCAAAAGCTTATACAGATGGAAAAATTAACATCGATCAC

TCTGGAGGATACGTTGCTCAATTCAACATTTCTTGGGATGAAGTAAATTATGAT

U .044 I ;i m i no iici d sequ nc si:o ID \o - m

MKKIMLVFITLILVSLPIAQQTEAKDASAF KENSISSMAPPASPPASPKTPIEKKHADEI DKYIQGLDY KNNVLVYHGDAVTNVPPRKGYKDG EYIVVEKKKKSINQNNADIQV VNAISSLTYPGALVK ANSEL VENQPDVLPVKRDSLTLSIDLPGMTNQD KIVVKNATK SNVNNAVNTLVERWNEKYAQAYPNVSAKIDYDDEMAYSESQLIAKFGTAFKAVNNS LNVNFGAISEGKMQEEVISFKQIYYNVNVNEPTRPSRFFGKAVTKEQLQALGVNAENP P AYIS S VAYGRQ VYLKLSTNSHSTKVKAAFD AAVSGKS VSGDVELTNIIKNS SFKAVIY GGSAKDEVQIIDGNLGDLRDILKKGATFNRETPGVPIAYTTNFLKDNELAVIKNNSEYI ETTSKAYTDGKINIDHSGGYVAQFNISWDEVNYD

1 H ) 4 I. \I 'I.S1 nucl eoti de sequence ( Sl !O I D \() 5» )

ATGAAAAAAATAATGCTAGTTTTTATTACACTTATATTAGTTAGTCTACCAATTGC

GCAACAAACTGAAGCAAAGGATGCATCTGCATTCAATACGCCAATCGAAAAGAA

ACACGCGGATGAAATCGATAAGTATATACAAGGATTGGATTACAATAAAAACAAT

GTATTAGTATACCACGGAGATGCAGTGACAAATGTGCCGCCAAGAAAAGGTTACA

AAGATGGAAATGAATATATTGTTGTGGAGAAAAAGAAGAAATCCATCAATCAAA

ATAATGCAGACATTCAAGTTGTGAATGCAATTTCGAGCCTAACCTATCCAGGTGCT

CTCGTAAAAGCGAATTCGGAATTAGTAGAAAATCAACCAGATGTTCTCCCTGTAA

AACGTGATTCATTAACACTCAGCATTGATTTGCCAGGTATGACTAATCAAGACAAT

AAAATAGTTGTAAAAAATGCCACTAAATCAAACGTTAACAACGCAGTAAATACAT

TAGTGGAAAGATGGAATGAAAAATATGCTCAAGCTTATCCAAATGTAAGTGCAAA

AATTGATTATGATGACGAAATGGCTTACAGTGAATCACAATTAATTGCGAAATTT

GGTACAGCATTTAAAGCTGTAAATAATAGCTTGAATGTAAACTTCGGCGCAATCA

GTGAAGGGAAAATGCAAGAAGAAGTCATTAGTTTTAAACAAATTTACTATAACGT

GAATGTTAATGAACCTACAAGACCTTCCAGATTTTTCGGCAAAGCTGTTACTAAAG

AGCAGTTGCAAGCGCTTGGAGTGAATGCAGAAAATCCTCCTGCATATATCTCAAG

TGTGGCGTATGGCCGTCAAGTTTATTTGAAATTATCAACTAATTCCCATAGTACTA

AAGTAAAAGCTGCTTTTGATGCTGCCGTAAGCGGAAAATCTGTCTCAGGTGATGT

AGAACTAACAAATATCATCAAAAATTCTTCCTTCAAAGCCGTAATTTACGGAGGTT CCGCAAAAGATGAAGTTCAAATCATCGACGGCAACCTCGGAGACTTACGCGATAT

TTTGAAAAAAGGCGCTACTTTTAATCGAGAAACACCAGGAGTTCCCATTGCTTATA

CAACAAACTTCCTAAAAGACAATGAATTAGCTGTTATTAAAAACAACTCAGAATA

TATTGAAACAACTTCAAAAGCTTATACAGATGGAAAAATTAACATCGATCACTCT

GGAGGATACGTTGCTCAATTCAACATTTCTTGGGATGAAGTAAATTATGAT

1 . I .Q44 1 MM - ST am i no aci d sequence ( SI !Q I I ) \() 5 1 )

MKKIMLVFITLILVSLPIAQQTEAKDASAFNTPIEKKHADEIDKYIQGLDY KNNVLVY HGDAVTNVPPRKGYKDG EYIVVEKKKKSINQNNADIQVVNAISSLTYPGALVKANS ELVENQPDVLPVKRDSLTLSIDLPGMTNQD KIVVKNATKSNVNNAVNTLVERW E K Y AQ A YPN VS AKID YDDEM A YSES QLIAKF GT AFK A VNN SLNV F GAI SEGKMQEE V I SFKQI Y YNVNVNEPTRP SRFF GK A VTKEQLQ ALGVN AENPP A YI S S V A YGRQ V YLKL STNSHSTKVKAAFDAAVSGKSVSGDVELTNIIKNSSFKAVIYGGSAKDEVQIIDGNLGD LRDILKKGATFNRETPGVPIAYTTNFLKDNELAVIKNNSEYIETTSKAYTDGKINIDHSG GY V AQFNI S WDE VN YD

/ / O-f-f l l-V ⁾ nucl eoti de se uence ( S I !Q I I ) \( ) 52 )

ATGAAAAAAATAATGCTAGTTTTTATTACACTTATATTAGTTAGTCTACCAATTGC

GCAACAAACTGAAGCAAAGGATGCATCTGCATTCAATAAAGAAGAAATCGATAA

GTATATACAAGGATTGGATTACAATAAAAACAATGTATTAGTATACCACGGAGAT

GCAGTGACAAATGTGCCGCCAAGAAAAGGTTACAAAGATGGAAATGAATATATT

GTTGTGGAGAAAAAGAAGAAATCCATCAATCAAAATAATGCAGACATTCAAGTTG

TGAATGCAATTTCGAGCCTAACCTATCCAGGTGCTCTCGTAAAAGCGAATTCGGA

ATTAGTAGAAAATCAACCAGATGTTCTCCCTGTAAAACGTGATTCATTAACACTCA

GCATTGATTTGCCAGGTATGACTAATCAAGACAATAAAATAGTTGTAAAAAATGC

CACTAAATCAAACGTTAACAACGCAGTAAATACATTAGTGGAAAGATGGAATGAA

AAATATGCTCAAGCTTATCCAAATGTAAGTGCAAAAATTGATTATGATGACGAAA

TGGCTTACAGTGAATCACAATTAATTGCGAAATTTGGTACAGCATTTAAAGCTGTA

AATAATAGCTTGAATGTAAACTTCGGCGCAATCAGTGAAGGGAAAATGCAAGAA

GAAGTCATTAGTTTTAAACAAATTTACTATAACGTGAATGTTAATGAACCTACAAG

ACCTTCCAGATTTTTCGGCAAAGCTGTTACTAAAGAGCAGTTGCAAGCGCTTGGA

GTGAATGCAGAAAATCCTCCTGCATATATCTCAAGTGTGGCGTATGGCCGTCAAG

TTTATTTGAAATTATCAACTAATTCCCATAGTACTAAAGTAAAAGCTGCTTTTGAT

GCTGCCGTAAGCGGAAAATCTGTCTCAGGTGATGTAGAACTAACAAATATCATCA

AAAATTCTTCCTTCAAAGCCGTAATTTACGGAGGTTCCGCAAAAGATGAAGTTCA

AATCATCGACGGCAACCTCGGAGACTTACGCGATATTTTGAAAAAAGGCGCTACT

TTTAATCGAGAAACACCAGGAGTTCCCATTGCTTATACAACAAACTTCCTAAAAG

ACAATGAATTAGCTGTTATTAAAAACAACTCAGAATATATTGAAACAACTTCAAA

AGCTTATACAGATGGAAAAATTAACATCGATCACTCTGGAGGATACGTTGCTCAA

TTCAACATTTCTTGGGATGAAGTAAATTATGAT

I . I .Q44 I \2o ami no aci d sequence ( S I !Q I I ) \( ) 53 )

MKKF LVFITLILVSLPIAQQTEAKDASAFNKEEIDKYIQGLDYNKNNVLVYHGDAVT NWPRKGYKDGNEYIVVEKKKKSINQNNADIQVVNAISSLTYPGALVK ANSEL VENQP D VLP VKRD SLTL SIDLPGMTNQDNKI VVKNATK SNVNNAVNTL VERWNEK YAQ AYP NVSAKIDYDDEMAYSESQLIAKFGTAFKAVNNSLNVNFGAISEGKMQEEVISFKQIYY NVNVNEPTR SREFGKA VTKEQLQ ALGVN AENPP AYISSVA YGRQ VYLKLSTNSHST KVKAAFDAAVSGKSVSGDVELTNIIKNSSFKAVIYGGSAKDEVQIIDGNLGDLRDILK KGATFNRETPGVPIAYTTNFLKDNELAVIKNNSEYIETTSKAYTDGKINIDHSGGYVAQ FNI S WDEVN YD

. U l. l.X/nn nucleotide sequence ( S I X) I I ) \() 5^ ) GTGGGATTAAATAGATTTATGCGTGCGATGATGGTAGTTTTCATTACTGCCAACTG

CATTACGATTAACCCCGACATAATATTTGCAGCGACAGATAGCGAAGATTCCAGT

CTAAACACAGATGAATGGGAAGAAGAAAAAACAGAAGAGCAGCCAAGCGAGGT

AAATACGGGACCAAGATACGAAACTGCACGTGAAGTAAGTTCACGTGATATTGAG

GAACTAGAAAAATCGAATAAAGTGAAAAATACGAACAAAGCAGACCTAATAGCA

ATGTTGAAAGCAAAAGCAGAGAAAGGT

\cl \ \ I ' m ami no aci d sequence ( S I X.) I I ) \( ) ^Q " )

MGLNREMRAMMV IT ANCITINPDIIF AATD SED S SLNTDEWEEEKTEEQP SEVNTGP RYET AREVS SRDIEELEK S K VKNT K ADLI AMLK AK AEKG

[00368] In some embodiments, the present invention relates to a fusion protein comprising an epidermal growth factor receptor variant III (EGFRvIII) polypeptide and a synovial sarcoma, X breakpoint 2 (SSX2) polypeptide. In some embodiments, said EGFRvIII polypeptide comprises an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6. In some embodiments, said fusion protein comprises a plurality of EGFRvIII polypeptides. In some embodiments, said fusion protein comprises five copies of the EGFRvIII polypeptide. In certain embodiments, said EGFRvIII polypeptide is flanked by one or more cleaver sequences. In certain embodiments, the EGFRvIII polypeptide is fused to the N-terminus of the SSX2 polypeptide. In certain embodiments, the SSX2 polypeptide comprises an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to SSX2 as set forth in SEQ ID NO: 10.

[00369] In some embodiments, the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to SSX2 as set forth in SEQ ID NO: 10. In certain embodiments, the fusion protein comprises an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx5-SSX2 as set forth in amino acid residues 89 to 475 of SEQ ID NO:4.

[00370] In some embodiments, the fusion protein comprises a signal sequence, wherein the signal sequence is in translational reading frame with the EGFRvIII polypeptide and the SSX2 polypeptide. In certain embodiments, the signal sequence is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2. [00371] In certain embodiments, said fusion protein is expressed in a bacterium. In one embodiment, the bacterium is Listeria monocytogenes.

[00372] In various embodiments, the present invention also provides nucleic acid molecule encoding the fusion protein of any of the preceding embodiments.

[00373] In certain embodiments, said nucleic acid molecule comprises one or more EGFRvIII polynucleotides that are at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO: 5 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the SSX2 polynucleotide as set forth in SEQ ID NO:9.

[00374] In some embodiments, the nucleic acid molecule further comprises a promoter, a signal sequence, or both, wherein the promoter, signal sequence, or both are operably linked with the nucleotide sequence encoding the EGFRvIII polypeptide and the nucleotide sequence encoding the SSX2 polypeptide. In certain embodiments, the promoter is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to an actA promoter as set forth in SEQ ID NO:21. In various embodiments, the signal sequence is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN 100* as set forth in SEQ ID NO: 1. In some embodiments, the nucleic acid molecule is part of an expression cassette.

[00375] In some embodiments, the present invention provides a vector comprising the nucleic acid molecule of any of the preceding embodiments.

[00376] In some embodiments, the present invention also provides a host cell comprising the nucleic acid molecule of any of the preceding embodiments. In certain embodiments, said host cell is a bacterium. In one embodiment, the bacterium is Listeria monocytogenes. In some embodiments, the Listeria monocytogenes is an actA deletion mutant, an actA insertion mutant, an inlB deletion mutant, an inlB insertion mutant, or a combination thereof. In one embodiment, the Listeria monocytogenes is a AactA/AinlB mutant. In certain embodiments, the nucleic acid molecule is integrated into the host cell genome. In certain embodiments, the nucleic acid molecule is integrated into the actA locus, inlB locus or tRNA ^Arg locus.

[00377] In various embodiments, the host cell of any of the preceding embodiments is in combination with a pharmaceutically acceptable excipient.

[00378] In some embodiments, the present invention provides a vaccine comprising the host cell of any of the preceding embodiments and a pharmaceutically acceptable excipient. [00379] In certain embodiments, the present invention provides a fusion protein comprising an EGFRvIII polypeptide and a prostatic acid phosphatase (PAP) polypeptide. In some embodiments, said EGFRvIII polypeptide comprises an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6. In certain embodiments, said fusion protein comprises a plurality of EGFRvIII polypeptides. In one embodiment, said fusion protein comprises five copies of the EGFRvIII polypeptide.

[00380] In certain embodiments, said EGFRvIII polypeptide is flanked by one or more cleaver sequences. In some embodiments, the EGFRvIII polypeptide is fused to the N- terminus of the PAP polypeptide.

[00381] In some embodiments, the PAP polypeptide comprises an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14. In certain embodiments, the fusion protein comprises an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx5-PAP33.386 as set forth in amino acid residues 89 to 606 SEQ ID NO: 12.

[00382] In certain embodiments, the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14.

[00383] In some embodiments, the fusion protein further comprises a signal sequence, wherein the signal sequence is in translational reading frame with the EGFRvIII polypeptide and the PAP polypeptide. In certain embodiments, the signal sequence is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth in SEQ ID NO:2.

[00384] In various embodiments, the fusion protein is expressed in a bacterium. In some embodiments, the bacterium is Listeria monocytogenes.

[00385] In certain embodiments, the present invention provides a nucleic acid molecule encoding the fusion protein of any of the preceding embodiments. In some embodiments, said nucleic acid molecule comprises one or more EGFRvIII polynucleotides that are at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the PAP 33-386 polynucleotide as set forth in SEQ ID NO: 13.

[00386] In some embodiments, the nucleic acid further comprises a promoter, a signal sequence, or both, wherein the promoter, signal sequence, or both are in translational frame with the nucleotide sequence encoding the EGFRvIII polypeptide and the nucleotide sequence encoding the PAP polypeptide. In certain embodiments, the promoter is at least i) 90%) identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to an actA promoter as set forth in SEQ ID NO:21. In some embodiments, the signal sequence is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN 100* as set forth in SEQ ID NO: 1.

[00387] In one embodiment, said nucleic acid molecule is part of an expression cassette.

[00388] In certain embodiments, the present invention provides a vector comprising the nucleic acid molecule of any of the preceding embodiments.

[00389] In some embodiments, the present invention provides a host cell comprising the nucleic acid molecule of any of the preceding embodiments. In certain embodiments, said host cell is a bacterium. In one embodiment, the bacterium is Listeria monocytogenes. In various embodiments, the Listeria monocytogenes is an actA deletion mutant, an actA insertion mutant, an inlB deletion mutant, an inlB insertion mutant, or a combination thereof. In one embodiment, the Listeria monocytogenes is a AactA/AinlB mutant.

[00390] In some embodiments, the nucleic acid molecule is integrated into the host cell genome. In certain embodiments, the nucleic acid molecule is integrated into the actA locus, inlB locus or tRNA ^Arg locus.

[00391] In certain embodiments, the host cell is in combination with a pharmaceutically acceptable excipient.

[00392] In some embodiments, the present invention provides a vaccine comprising the host cell of any of the preceding embodiments and a pharmaceutically acceptable excipient.

[00393] In certain embodiments, the present invention provides a fusion protein comprising an EGFRvIII polypeptide, an NK3 homeobox 1 (NKX3.1) polypeptide, and a prostate-specific membrane antigen (PSMA) polypeptide. In some embodiments, said EGFRvIII polypeptide comprises an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6. In some embodiments, the fusion protein comprises a plurality of EGFRvIII polypeptides. In one embodiment, the fusion protein comprises five copies of the EGFRvIII polypeptide. [00394] In some embodiments, said EGFRvIII polypeptide is flanked by one or more cleaver sequences.

[00395] In certain embodiments, the EGFRvIII polypeptide is fused to the N-terminus of the NKX3.1 polypeptide, and wherein the NKX3.1 polypeptide is fused to the N-terminus of the PSMA polypeptide.

[00396] In some embodiments, the PSMA polypeptide comprises an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi. 20, 44-138, 169-750 as set forth in SEQ ID NO:20.

[00397] In certain embodiments, the NKX3.1 polypeptide comprises an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.111.234 as set forth in SEQ ID NO:25.

[00398] In certain embodiments, the NKX3.1 polypeptide comprises an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.111.234 (R41 G) as set forth in SEQ ID NO : 18.

[00399] In some embodiments, the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 n. ₂₃ 4 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20 , 44-138, 169-750 as set forth in SEQ ID NO:20.

[00400] In one embodiment, the fusion protein comprises an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5- NKX3. l ii.234-PSMAi.2o, 44-i3 ₈ , 169-750 as set forth in amino acid residues 89 to 1177 of SEQ ID NO:23.

[00401] In certain embodiments, the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 (R41 G) 11.234 as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%. identical to PSMAi. ₂₀ , 44-138, 169-750 as set forth in SEQ ID NO:20. [00402] In some embodiments, the fusion protein comprises an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

EGFRvIIIx5- KX3.1(R41G)ii-234-PSMAi-2o, 44-138, 169-750 as set forth in amino acid residues 89 to 1177 of SEQ ID NO: 16.

[00403] In some embodiments, the fusion protein further comprises a signal sequence, wherein the signal sequence is in translational reading frame with the EGFRvIII polypeptide, NKX3.1 polypeptide, and the PSMA polypeptide. In some embodiments, the signal sequence is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth in SEQ ID NO:2.

[00404] In various embodiments, the fusion protein is expressed in a bacterium. In one embodiment, the bacterium is Listeria monocytogenes.

[00405] In some embodiments, the present invention provides a nucleic acid molecule encoding the fusion protein of any of the preceding embodiments. In certain embodiments, said nucleic acid molecule comprises one or more EGFRvIII polynucleotides that are at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5, a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3.I _n . ₂₃ 4 polynucleotide as set forth in SEQ ID NO:24, and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the PSMA 1.20, 44-138, 169-750 as set forth in SEQ ID NO: 19.

[00406] In some embodiments, nucleic acid molecule comprises one or more EGFRvIII polynucleotides that are at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the EGFRvIII polynucleotide as set forth in SEQ ID NO:5, a

polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the NKX3 (R41G) _n . ₂ 34 polynucleotide as set forth in SEQ ID NO: 17, and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to the PSMA j. ₂₀ , 44- , 169-750 as set forth in SEQ ID NO: 19.

[00407] In some embodiments, the nucleic acid further comprises a promoter, a signal sequence, or both, wherein the promoter, signal sequence, or both are in translational frame with the nucleotide sequence encoding the EGFRvIII polypeptide, NKX3.1 polypeptide, and the PSMA polypeptide. In some embodiment, the promoter is at least i) 90% identical, ii) 95%) identical, iii) 99% identical, or iv) 100% identical to an actA promoter as set forth in SEQ ID NO:21. In some embodiments, the signal sequence is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN 100* as set forth in SEQ ID NO: l .

[00408] In some embodiments, the nucleic acid molecule of any of the preceding embodiments is part of an expression cassette.

[00409] In some embodiments, the present invention provides a vector comprising the nucleic acid molecule of any of the preceding embodiments.

[00410] In some embodiments, the present invention provides a host cell comprising the nucleic acid molecule of any of the preceding embodiments. In some embodiments, host cell is a bacterium. In one embodiment, the bacterium is Listeria monocytogenes. In some embodiments, the Listeria monocytogenes is an actA deletion mutant, an actA insertion mutant, an inlB deletion mutant, an inlB insertion mutant, or a combination thereof. In some embodiments, the Listeria monocytogenes is a AactA/AinlB mutant.

[00411] In some embodiments, the nucleic acid molecule is integrated into the host cell genome. In some embodiments, the nucleic acid molecule is integrated into the actA locus, inlB locus or tRNA ^Arg locus.

[00412] In some embodiments, the host cell of any of the preceding embodiments is in combination with a pharmaceutically acceptable excipient.

[00413] In various embodiments, the present invention provides a vaccine comprising the host cell of any of the preceding embodiments and a pharmaceutically acceptable excipient.

[00414] In some embodiments, the present invention provides a fusion protein comprising an K3 homeobox 1 ( KX3.1) polypeptide and a PAP polypeptide. In some embodiments, the KX3.1 polypeptide comprises an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to KX3.1 as set forth in SEQ ID NO:29.

[00415] In some embodiments, the KX3.1 polypeptide is fused to the N-terminus of the PAP polypeptide.

[00416] In some embodiments, the PAP polypeptide comprises an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14.

[00417] In some embodiments, the fusion protein comprises an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1- PAP ₃₃ -386 as set forth in amino acid residues 89 to 678 of SEQ ID NO:27.

[00418] In some embodiments, the fusion protein comprises a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to KX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14.

[00419] In some embodiments, the fusion protein further comprises a signal sequence, wherein the signal sequence is in translational reading frame with the NKX3.1 polypeptide and the PAP polypeptide. In some embodiments, the signal sequence is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth in SEQ ID NO:2.

[00420] In some embodiments, said fusion protein is expressed in a bacterium. In one embodiment, the bacterium is Listeria monocytogenes.

[00421] In some embodiments, the present invention provides a nucleic acid molecule encoding the fusion protein of any of the preceding embodiments. In some embodiments, said nucleic acid molecule comprises a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%> identical to the NKX3.1 polynucleotide as set forth in SEQ ID NO:28 and a polynucleotide that is at least i) 90% identical, ii) 95% identical, iii) 99%) identical, or iv) 100%> identical to the PAP 33.386 polynucleotide as set forth in SEQ ID NO: 13.

[00422] In some embodiments, the nucleic acid further comprises a promoter, a signal sequence, or both, wherein the promoter, signal sequence, or both are in translational frame with the nucleotide sequence encoding the NKX3.1 polypeptide and the nucleotide sequence encoding the PAP polypeptide. In some embodiments, the promoter is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to an actA promoter as set forth in SEQ ID NO:21. In some embodiments, the signal sequence is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth in SEQ ID NO: 1.

[00423] In some embodiments, said nucleic acid molecule being part of an expression cassette.

[00424] In some embodiments, the present invention provides a vector comprising the nucleic acid molecule of any of the preceding embodiments.

[00425] In some embodiments, the present invention provides a host cell comprising the nucleic acid molecule of any of the preceding. In one embodiment, said host cell is a bacterium. In some embodiments, the bacterium is Listeria monocytogenes. In some embodiments, the Listeria monocytogenes is an actA deletion mutant, an actA insertion mutant, an inlB deletion mutant, an inlB insertion mutant, or a combination thereof. In certain embodiments, the Listeria monocytogenes is a AactA/AinlB mutant. In some embodiments, the nucleic acid molecule is integrated into the host cell genome. In various embodiments, the nucleic acid molecule is integrated into the actA locus, MB locus or tRNA ^Arg locus.

[00426] In some embodiments, the host cell of any of the preceding embodiments is in combination with a pharmaceutically acceptable excipient.

[00427] In some embodiments, the present invention provides a vaccine comprising the host cell of any of the preceding embodiments and a pharmaceutically acceptable excipient.

[00428] In some embodiments, the present invention provides a host cell comprising one or more nucleic acid molecules, said nucleic acid molecules comprising a nucleic acid sequence encoding: a) an EGFRvIII-SSX2 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10; b) an EGFRvIII-PAP33.386 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP33-386 as set forth in SEQ ID NO: 14; c) an EGFRvIII- NKX3.111.234-PSMA1.20, 44-138, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 n. ₂₃ 4 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to PSMA1.20, 44.138, 169-750 as set forth in SEQ ID NO:20; d) an EGFRvIII-NKX3.1(R41G)ii.234-PSMAi. ₂ o, 4-138, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to SEQ ID NO:6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 (R41 G) 11.234 as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20, 44-138, 169-750 as set forth in SEQ ID NO:20; e) a NKX3.1-PAP33- 386 fusion protein, wherein the fusion protein comprises a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14; f) an ActAN100*-SSX2 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10; g) an ActANlOO- PAP ₃₀ -386 fusion protein, wherein the fusion protein comprises an ActANlOO polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to amino acid residues 1 to 100 of SEQ ID NO:33 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99%) identical, or iv) 100%) identical to PAP ₃₀ -386 as set forth in amino acid residues 103- 459 of SEQ ID NO:33; or h) any combination thereof.

[00429] In some embodiments, the nucleic acid molecules of the host cell comprises: a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3; b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃₈ 6 as set forth in SEQ ID NO: 11; c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%> identical to EGFFvIIIx5-NKX3.1n-234-PSMAi-2o, 44-m 169-750 as set forth in SEQ ID NO:22; d) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G) ₁₁ -234-PSMA ₁ . ₂ o, ₄ 4-m. -750 as set forth in SEQ ID NO: 15; e) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP 33-386 as set forth in SEQ ID NO:26; f) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:30; g) a nucleic acid sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-PAP ₃₀ -386-SL8 as set forth in SEQ ID NO:32; h) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIxl -PAP '33-386 as set forth in SEQ ID NO:34; i) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx2-PAP 33-386 as set forth in SEQ ID NO:36; j) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx 3- PAP ₃₃ .386 as set forth in SEQ ID NO:38; k) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx4-PAP '33-386 as set forth in SEQ ID NO:40; or 1) any combination thereof.

[00430] In some embodiments, the host cell is a bacterium. In one embodiment, the bacterium is Listeria monocytogenes. In some embodiments, the Listeria monocytogenes is a AactA/AinlB mutant.

[00431] In some embodiments, the host cell of any of the preceding embodiments comprises: a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3; b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP 33-386 as set forth in SEQ ID NO: 11; and c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1 n^-PSMA^o, 44-138, m-750 as set forth in SEQ ID NO:22. In some embodiments, (a) is integrated into the actA locus, (b) is integrated into the inlB locus, and (c) is integrated into the tRNA ^Arg locus.

[00432] In some embodiments, the host cell of any of the preceding embodiments comprises: a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3; b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP 33-386 as set forth in SEQ ID NO: 11; and c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G) ₁₁ -234-PSMA ₁ . ₂ o, 44-iss. -750 as set forth in SEQ ID NO: 15. In some embodiments, (a) is integrated into the actA locus, (b) is integrated into the inlB locus, and (c) is integrated into the tRNA ^Arg locus.

[00433] In some embodiments, the host cell of any of the preceding embodiments comprises: a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP 33-386 as set forth in SEQ ID NO:26; and b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3. In some

embodiments, (a) is integrated into the inlB locus, and (b) is integrated into the tRNA ^Arg locus.

[00434] In some embodiments, the host cell of any of the preceding embodiments comprises: a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP ₃₃ -386 as set forth in SEQ ID NO:26; and b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:30. In some

embodiments, (a) is integrated into the inlB locus, and (b) is integrated into the tRNA ^Arg locus.

[00435] In some embodiments, the nucleic acid molecules of the host cell of any of the preceding embodiments comprise a nucleic acid sequence encoding: a) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in amino acid residues 89 to 475 of SEQ ID NO:4; b) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx5-PAP ₃₃ .3 ₈ 6 as set forth in amino acid residues 89 to 606 of SEQ ID NO: 12; c) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx5-NKX3.1 ₁₁ . ₂₃₄ -PSMA ₁ . _{20; 44} . ₁₃ 8, 169-750 as set forth in amino acid residues 89 to 1177 of SEQ ID NO:23; d) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5- NKX3.1(R41G)ii.234-PSMAi.2o, 44-i3 ₈ , 169-750 as set forth in amino acid residues 89 to 1177 of SEQ ID NO: 16; e) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99%) identical, or iv) 100%) identical to NKX3. l-PAP ₃₃ .3s6 as set forth in amino acid residues 89 to 678 of SEQ ID NO:27; f) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:31; g) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to ActAN100*-PAP3 ₀ -3 ₈ 6 as set forth in amino acid residues 1- 459 of SEQ ID NO:33; h) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99%) identical, or iv) 100%) identical to EGFRvIIIxl-PAP ₃₃ .3 ₈₆ as set forth in amino acid residues 89 to 476 of SEQ ID NO:35; i) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx2-PAP ₃ 3-3 ₈ 6 as set forth in amino acid residues 89 to 509 of SEQ ID NO:37; j) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx3-PAP ₃ 3-3 ₈ 6 as set forth in amino acid residues 89 to 541 of SEQ ID NO: 39; k) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

EGFRvIIIx4-PAP ₃ 3-386 as set forth in amino acid residues 89 to 573 of SEQ ID NO:41; or 1) any combination thereof.

[00436] In some embodiments, the present invention provides a method of eliciting an immune response in a subject comprising administering to the subject a composition comprising the host cell of any of the preceding embodiments.

[00437] In some embodiments, the present invention provides a method of eliciting an immune response in a subject comprising, administering to the subject a composition comprising a host cell, wherein the host cell expresses one or more fusion proteins comprising: a) an EGFRvIII-SSX2 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10; b) an EGFRvIII-PAP _33-3 86 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP _33-386 as set forth in SEQ ID NO: 14; c) an EGFRvIII- NKX3.1 ii.2 ₃ 4-PSMAi.2o, ₄₄ - ₁₃₈ , 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 n _-234 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-2 o, ₄₄ - ₁₃₈ , 169-750 as set forth in SEQ ID NO:20; d) an EGFRvIII-NKX3.1(R41G)ii _-234 -PSMAi _-2 o, 4-138, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to SEQ ID NO:6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3. l(R41G)ii-234 as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20, 44-138, 169-750 as set forth in SEQ ID NO:20; e) a NKX3.1-PAP33- 386 fusion protein, wherein the fusion protein comprises a KX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to KX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14; f) an ActAN100*-SSX2 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10; g) an ActANlOO*- PAP ₃₀ -386 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to PAP _30- 386 as set forth in amino acid residues 103- 459 of SEQ ID NO:33; or h) any combination thereof.

[00438] In some embodiments, the one or more fusion proteins are expressed from a nucleic acid molecule comprising: a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3; b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 11; c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1 _n _ ₂ 34-PSMA ₁ - ₂ o, 44-m, 109-750 as set forth in SEQ ID NO:22; d) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G) ₁₁ . ₂₃ 4-PSMA ₁ .2o, 44-m, m- 750 as set forth in SEQ ID NO: 15; e) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 -PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:26; f) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:30; g) a nucleic acid sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-PAP ₃₀ - ₃₈ 6-SL8 as set forth in SEQ ID NO:32; h) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIxl-PAP ₃₃ -386 as set forth in SEQ ID NO:34; i) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx2-PAP '33-386 as set forth in SEQ ID NO:36; j) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx3-PAP 33-386 as set forth in SEQ ID NO:38; k) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx4- PAP ₃₃ .386 as set forth in SEQ ID NO:40; or 1) any combination thereof. In some

embodiments, (a) is integrated into the actA locus, (b) is integrated into the MB locus, and (c) is integrated into the tRNA ^Arg locus. In certain embodiments, (a) is integrated into the actA locus, (b) is integrated into the inlB locus, and (d) is integrated into the tRNA ^Arg locus. In some embodiments, (e) is integrated into the MB locus, and (f) is integrated into the tRNA ^Arg locus. In various embodiments, (e) is integrated into the MB locus and (a) is integrated into the tRNA ^Arg locus.

[00439] In some embodiments, the one or more fusion proteins comprise: a) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in amino acid residues 89 to 475 of SEQ ID NO:4; b) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx5-PAP ₃₃ .3 ₈ 6 as set forth in amino acid residues 89 to 606 of SEQ ID NO: 12; c) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvinx5-NKX3.1 ₁₁ . ₂₃₄ -PSMA ₁ . _{20; 44} . ₁₃ 8, 169-750 as set forth in amino acid residues 89 to 1177 of SEQ ID NO:23; d) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5- NKX3.1(R41G)ii-234-PSMAi.2o, 44-i3 ₈ , 169-750 as set forth in amino acid residues 89 to 1177 of SEQ ID NO: 16; e) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3. l-PAP ₃₃ .3s6 as set forth in amino acid residues 89 to 678 of SEQ ID NO:27; f) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIxl-PAP ₃₃ .3 ₈ 6 as set forth in amino acid residues 89 to 476 of SEQ ID NO:35; g) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx2-PAP ₃ 3-3 ₈ 6 as set forth in amino acid residues 89 to 509 of SEQ ID NO:37; h) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

EGFRvIIIx3-PAP ₃ 3-3 ₈ 6 as set forth in amino acid residues 89 to 541 of SEQ ID NO: 39; i) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx4-PAP33.3 ₈₆ as set forth in amino acid residues 89 to 573 of SEQ ID NO:41; or j) any combination thereof.

[00440] In some embodiments of any of the preceding methods, said host cell is a bacterium. In one embodiment, the bacterium is Listeria monocytogenes. In certain embodiments, the Listeria monocytogenes is a AactA/AinlB mutant. In various embodiments, the administering step is performed intravenously. In some embodiments, the one or more fusion proteins are expressed and secreted from the host cell in the cytosol of an infected cell within the subject. In some embodiments, the infected cell is an antigen presenting cell.

[00441] In some embodiments, the present invention provides a method of increasing expression of an antigenic polypeptide, said method comprising expressing in a host cell a nucleic acid molecule, said nucleic acid molecule comprising a nucleic acid sequence encoding: a) an EGFRvIII-SSX2 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10; b) an EGFRvIII-PAP33.3 ₈₆ fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -3 ₈ 6 as set forth in SEQ ID NO: 14; c) an EGFRvIII- NKX3.111.234-PSMA1.20, ₄₄ - ₁₃₈ , 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO: 6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 n. ₂₃ 4 as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to PSMA1.20, ₄₄ - ₁₃₈ , 169-750 as set forth in SEQ ID NO:20; d) an EGFRvIII-NKX3.1(R41G)ii.234-PSMAi. ₂ o, 4-138, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to SEQ ID NO:6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 (R41 G) 11.234 as set forth in SEQ ID NO: 18, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _-20, 44-138, 169-750 as set forth in SEQ ID NO:20; e) a NKX3.1-PAP33- 386 fusion protein, wherein the fusion protein comprises a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -386 as set forth in SEQ ID NO: 14; f) an ActAN100*-SSX2 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10; g) an ActANlOO*- PAP ₃₀ -386 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to PAP ₃₀ -386 as set forth in amino acid residues 103- 459 of SEQ ID NO:33; or h) any combination thereof.

[00442] In certain embodiments, the one or more nucleic acid molecules comprise: a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3; b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃₈ 6 as set forth in SEQ ID NO: 11; c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%> identical to EGFFvIIIx5-NKX3.1n-234-PSMAi-2o, 44-m 169-750 as set forth in SEQ ID NO:22; d) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G) ₁₁ -234-PSMA ₁ . ₂ o, ₄ 4-m. -750 as set forth in SEQ ID NO: 15; e) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1-PAP 33-386 as set forth in SEQ ID NO:26; f) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:30; g) a nucleic acid sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-PAP ₃₀ -386-SL8 as set forth in SEQ ID NO:32; h) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIxl -PAP '33-386 as set forth in SEQ ID NO:34; i) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx2-PAP 33-386 as set forth in SEQ ID NO:36; j) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx 3- PAP ₃₃ .386 as set forth in SEQ ID NO:38; k) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx4-PAP '33-386 as set forth in SEQ ID NO:40; or 1) any combination thereof. In some embodiments, (a) is integrated into the actA locus, (b) is integrated into the inlB locus, and (c) is integrated into the tRNA ^Arg locus. In some embodiments, (a) is integrated into the actA locus, (b) is integrated into the inlB locus, and (d) is integrated into the tRNA ^Arg locus. In some embodiments, (e) is integrated into the MB locus, and (f) is integrated into the tRNA ^Arg locus. In some embodiments, (e) is integrated into the inlB locus and (a) is integrated into the tRNA ^Arg locus.

[00443] In some embodiments of any of the preceding methods, the nucleic acid molecules encode for fusion proteins comprising: a) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIII-SSX2 as set forth in amino acid residues 89 to 475 of SEQ ID NO:4; b) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIII-PAP _33-386 as set forth in amino acid residues 89 to 606 of SEQ ID NO: 12; c) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

EGFRvIII-NKX3. l n.234-PSMAi.2o, ₄₄ - ₁₃₈ , 169-750 as set forth in amino acid residues 89 to 1 177 of SEQ ID NO:23; d) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIII-NKX3.1(R41G)ii. ₂₃ 4-PSMAi -20, 44-l _38, 169-750 as set forth in amino acid residues 89 to 1 177 of SEQ ID NO: 16; e) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to

NKX3. l-PAP ₃₃ -3 ₈ 6 as set forth in amino acid residues 89 to 678 of SEQ ID NO:27; f) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to EGFRvIIIx 1-PAP ₃₃ .3 ₈₆ as set forth in amino acid residues 89 to 476 of SEQ ID NO:35; g) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx2-PAP ₃₃ .3 ₈ 6 as set forth in amino acid residues 89 to 509 of SEQ ID NO:37; h) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx3-PAP33.3 ₈ 6 as set forth in amino acid residues 89 to 541 of SEQ ID NO:39; i) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx4-PAP ₃ 3-3 ₈ 6 as set forth in amino acid residues 89 to 573 of SEQ ID NO:41; or j) any combination thereof.

[00444] In some embodiments of any of the preceding methods, said host cell is a bacterium. In certain embodiments, the bacterium is Listeria monocytogenes.

[00445] In some embodiments of any of the preceding methods the expressing step comprises infecting a cell of interest with the host cell. In some embodiments, said expressing step comprises administering the host cell to a subject.

[00446] In some embodiments, the nucleic acid molecule of any of the preceding host cell is inserted into an expression cassette on an episomal plasmid within the host cell.

[00447] In some embodiments, the nucleic acid molecules of any of the preceding host cell comprises EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3, EGFRvIIIx5-PAP 33-386 as set forth in SEQ ID NO: 11, and EGFRvIIIx5-NKX3. l(R41G) ₁₁ . ₂ 34-PSMA ₁ . ₂ o, ₄ 4-m, 169-750 as set forth in SEQ ID NO: 15.

[00448] In some embodiments, the nucleic acid molecules of any of the preceding host cell consist of EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3, EGFRvIIIx5-PAP 33-386 as set forth in SEQ ID NO: 11, and EGFRvIIIx5-NKX3.1(R41G) ₁₁ . ₂ 34-PSMA ₁ . ₂₀ , 44- , 169-750 as set forth in SEQ ID NO: 15.

[00449] In some embodiments of any of the preceding methods, the one or more nucleic acid molecules comprise: a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3; b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5 -PAP 33-386 as set forth in SEQ ID NO: 11; and c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G) ₁₁ - ₂ 3 ₄ -PSMA ₁ . ₂₀ , 44-m, m-750 as set forth in SEQ ID NO: 15.

[00450] In some embodiments of any of the preceding methods, the one or more nucleic acid molecules consist of EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3, EGFRvIIIx5- PAP 33-386 as set forth in SEQ ID NO: 11, and EGFRvIIIx5-NKX3.1(R41G) ₁₁ - ₂ 3 ₄ -PSMA ₁ . ₂₀ , ₄₄ - 138, 169-750 as set forth in SEQ ID NO: 15. [00451] In some embodiments, the present invention provides a method of treating cancer in a subject in need thereof, said method comprising administering to the subject a

therapeutically effective amount of a composition comprising a host cell, wherein the host cell expresses one or more fusion proteins comprising: a) an EGFRvIII-SSX2 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to SEQ ID NO:6 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10; b) an EGFRvIII-PAP ₃₃ .3 ₈ 6 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₃ -3 ₈ 6 as set forth in SEQ ID NO: 14; c) an EGFRvIII-NKX3.1 n-2 ₃ 4-PSMAi-2o, 44-i ₃₈ , 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 n. ₂₃₄ as set forth in SEQ ID NO:25, and a PSMA polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PSMAi _{-20, 4} 4-i _38, 169-750 as set forth in SEQ ID NO:20; d) an EGFRvIII-NKX3.1(R41G)ii _-23 4-PSMAi -20, 44-138, 169-750 fusion protein, wherein the fusion protein comprises one or more EGFRvIII

polypeptides comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SEQ ID NO:6, a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3. l(R41G)n _-234 as set forth in SEQ ID NO: 18, and a PSMA

polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100%) identical to PSMAi _-20; 44.13^ 169-750 as set forth in SEQ ID NO:20; e) a NKX3. l-PAP ₃₃ .3s6 fusion protein, wherein the fusion protein comprises a NKX3.1 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 as set forth in SEQ ID NO:29 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃ 3 _-38 6 as set forth in SEQ ID NO: 14; f) an ActAN100*-SSX2 fusion protein, wherein the fusion protein comprises an ActANlOO* polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO* as set forth as SEQ ID NO:2 and a SSX2 polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to SSX2 as set forth in SEQ ID NO: 10; g) an ActAN100-PAP ₃ o-386 fusion protein, wherein the fusion protein comprises an ActANlOO polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO as set forth in to amino acid residues 1 to 100 of SEQ ID NO:33 and a PAP polypeptide comprising an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to PAP ₃₀ - ₃ 86 as set forth in amino acid residues 103-459 of SEQ ID NO:33; or h) any combination thereof. In some embodiments, the host cell expresses (a), (b), and (d).

[00452] In some embodiments, the one or more fusion proteins are expressed from a nucleic acid molecule comprising: a) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3; b) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO: 11; c) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1 n^-PSMA^o, 44-iss, m-750 as set forth in SEQ ID NO:22; d) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G) ₁₁ .234-PSMA ₁ . ₂ o, ₄ 4-ns, m- 750 as set forth in SEQ ID NO: 15; e) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1 -PAP ₃₃ . ₃₈₆ as set forth in SEQ ID NO:26; f) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:30; g) a nucleic acid sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100-PAP ' ₃₀ - ₃₈ 6-SL8 as set forth in SEQ ID NO:32; h) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIxl -PAP ₃₃ . ₃₈ e as set forth in SEQ ID NO:34; i) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx2-PAP ₃₃ . ₃₈ 6 as set forth in SEQ ID NO:36; j) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx 3- PAP ₃₃ . ₃₈ 6 as set forth in SEQ ID NO:38; k) a nucleotide sequence that is at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx4-PAP ₃₃ -386 as set forth in SEQ ID NO:40; or 1) any combination thereof.

[00453] In some embodiments, the one or more fusion proteins are expressed from a nucleic acid molecule comprising (a), (b), and (d). In some embodiments, the one or more fusion proteins are expressed from a nucleic acid molecule consisting of (a), (b), and (d). In some embodiments, (a), (b), and (d) are operably linked to an ActA promoter. In some embodiments, the ActA promoter is set forth as SEQ ID NO:21. In some embodiments, (a) is integrated into the actA locus, (b) is integrated into the MB locus, and (c) is integrated into the tRNA ^Arg locus. In certain embodiments, (a) is integrated into the actA locus, (b) is integrated into the inlB locus, and (d) is integrated into the tRNA ^Arg locus. In some embodiments, (e) is integrated into the MB locus, and (f) is integrated into the tRNA ^Arg locus. In certain embodiments, (e) is integrated into the MB locus and (a) is integrated into the tRNA ^Arg locus.

[00454] In some embodiments, the one or more fusion proteins are expressed from a nucleic acid molecule consisting of EGFRvIIIx5-SSX2 as set forth in SEQ ID NO:3,

EGFRvIIIx5-PAP 33-386 as set forth in SEQ ID NO: 11, and EGFRvIIIx5-NKX3.1(R41G) _n . ₂ 34- PSMAi-20, 44-138, 169-750 as set forth in SEQ ID NO: 15.

[00455] In certain embodiments, the cancer is an EGFRvIII-expressing cancer, a SSX2- expressing cancer, a PAP-expressing cancer, a NKX3.1 -expressing cancer, a PSMA- expressing cancer, or any combination thereof. In one embodiment, the cancer is prostate cancer.

[00456] In certain embodiments, the host cell is Listeria monocytogenes. In various embodiemnts, the Listeria monocytogenes is an actA deletion (AactA) mutant, an actA insertion mutant, an MB deletion (AMB) mutant, an MB insertion mutant, or a combination thereof. In one embodiment, the Listeria monocytogenes is a AactA/AMB mutant.

[00457] In some embodiments of any of the preceding methods of treating cancer, the fusion protein is expressed and secreted from the host cell in the cytosol of an infected cell within the subject. In certain embodiments, the infected cell is an antigen presenting cell.

[00458] In some embodiments of any of the preceding methods of treating cancer, the one or more fusion proteins comprise: a) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-SSX2 as set forth in amino acid residues 89 to 475 of SEQ ID NO:4; b) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-PAP ₃ 3-386 as set forth in amino acid residues 89 to 606 of SEQ ID NO: 12; c) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5- NKX3. l n-234-PSMAi.2o, 44-138, 169-750 as set forth in amino acid residues 89 to 1177 of SEQ ID NO:23; d) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx5-NKX3.1(R41G)ii-234-PSMAi _-2 o, 44-i38, 169-750 as set forth in amino acid residues 89 to 1177 of SEQ ID NO: 16; e) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to NKX3.1- PAP ₃₃ .386 as set forth in amino acid residues 89 to 678 of SEQ ID NO:27; f) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActAN100*-SSX2 as set forth in SEQ ID NO:31; g) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to ActANlOO- PAP ₃₀ -386 as set forth in amino acid residues 1-459 of SEQ ID NO:33; h) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIxl-PAP ₃ 3-386 as set forth in amino acid residues 89 to 476 of SEQ ID NO:35; i) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx2-PAP _33-386 as set forth in amino acid residues 89 to 509 of SEQ ID NO:37; j) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx3-PAP ₃₃ .3 ₈ 6 as set forth in amino acid residues 89 to 541 of SEQ ID NO: 39; k) an amino acid sequence at least i) 90% identical, ii) 95% identical, iii) 99% identical, or iv) 100% identical to EGFRvIIIx4-PAP _33-386 as set forth in amino acid residues 89 to 573 of SEQ ID NO:41; or any combination thereof.

[00459] In some embodiments of any of the preceding methods of treating cancer, the one or more fusion proteins comprise (a), (b), and (d).

[00460] In some embodiments of any of the preceding methods of treating cancer, the one or more fusion proteins consist of (a), (b), and (d).

[00461] In some embodiments of any of the preceding methods of treating cancer, the one or more fusion proteins consist of EGFRvIIIx5-SSX2 as set forth in amino acid residues 89 to 475 of SEQ ID NO:4, EGFRvIIIx5-PAP ₃ 3-3 ₈ 6 as set forth in amino acid residues 89 to 606 of SEQ ID NO: 12, and EGFRvIIIx5-NKX3. l(R41G)n-234-PSMAi _-2 o, ₄₄ -i3 ₈ , 169-750 as set forth in amino acid residues 89 to 1177 of SEQ ID NO: 16.

[00462] In some embodiments, the method further comprises measuring expression of EGFRvIII, SSX2, PAP, NKX3.1, PSMA, or any combination thereof in a biological sample from the subject prior to administering the composition. [00463] In some embodiments of any of the preceding methods of treating cancer, the composition further comprises a pharmaceutically acceptable excipient. In certain embodiments, the administering step is performed intravenously.

[00464] In some embodiments, the method of treating cancer further comprises administering an antibiotic to the subject after administering the composition. In certain embodiments, the antibiotic is administered after a last dose of the composition. In related embodiments, the antibiotic is amoxicillin or trimethoprim/sulfamethoxazole.

[00465] The teachings of all patents, published applications and references cited herein are incorporated by reference in their entirety.

[00466] While this invention has been particularly shown and described with references to example embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the scope of the invention encompassed by the appended claims.