FIELD OF INVENTION

The present invention relates to the diagnosis of diseases related to the sodium-dependent multivitamin transporter/ solute carrier family 5 member 6 (SMVT! SLC5A6). In particular, the present invention relates to methods for measuring the level of SMVT in a biological sample using a receptor binding domain (RBD) ligand related to the envelope protein of porcine endogenous retrovirus type B (PERV-B).

BACKGROUND OF INVENTION

The sodium-dependent multivitamin transporter (SMVT), the product of the solute carrier family 5 member 6 (SLC5A6) gene, is a 12-pass transmembrane protein responsible for the cellular uptake of biotin, pantothenic acid and lipoic acid (Wang et al, J Biol Chem. 1999 May 2l;274(2l):l4875-83; Prasad et al, J Biol Chem. 1998 Mar 27;273(l3):750l- 6). As such, it plays an essential role in the synthesis and metabolism of proteins, carbohydrates and lipids. Biotin deficiency leads to a variety of clinical abnormalities, including for instance growth retardation, neurological disorders and dermatological disorders (Subramanian et al, Hum Genet. 2017 Feb;l36(2):253-26l) and animal studies have shown that biotin deficiencies during pregnancy lead to embryonic growth retardation, congenital malformation and death (Watanabe et al, Nutrition. 2009 Jan;25(l):78-84; Quick and Shi, Vitam Horm. 2015;98:63-100). Additionally, the inhibition of biotin uptake and a reduced activity of the SLC5A6 promoter in intestinal cells upon Salmonella infection has been reported (Ghosal et al, Am J Physiol Gastrointest Liver Physiol. 2015 Jul l5;309(2):Gl23-3l). Furthermore, SMVT expression is altered in several cancer cell lines suggesting its implication in cancer, in particular liver cancer, prostate cancer, lung cancer, gallbladder cancer, pancreas cancer, colon cancer, ovarian cancer, brain cancer, kidney cancer and lymphomas (see the Examples). Furthermore, SMVT gene expression has also been found altered in colon cancer (Provenzani et al, Carcinogenesis. 2006 Jul;27(7): 1323-33), V incristine-sensitive and resistant ovarian carcinoma cell lines (Buys et al , Genes Chromosomes Cancer. 2007 Dec;46(l2): 1069-79), prostate cancer (Sissung et al, Pharmacogenomics . 2016 Dec; 17(18): 1979-1986), lung adenocarcinoma (Leithner et al, PLoS One. 2016 Jun l3;l 1 (6):e0157453) and anaplastic thyroid carcinomas (Pita et al, J Clin Endocrinol Metab. 2014 Mar;99(3):E497-507). SMVT has also been considered as a potential target for drug delivery (Vadlapudi et al, Curr Drug Targets. 2012 Jun;l3(7):994-l003). Hence, beyond its interest in the determination of the metabolic state of a given cell, there is a need for a specific ligand targeting SMVT for its use in the diagnosis of SMVT- related diseases and drug targeting.

Here, the inventors demonstrated that a ligand related to the porcine endogenous retrovirus type B (PERV-B, that may also be referred to as porcine endogenous retrovirus subgroup B) envelope protein can bind specifically to SMVT. Several retrovirus envelope glycoproteins (Env) use nutrient transporters from the solute carrier family as receptors. The SLC-Env binding is mediated by the receptor binding domain (RBD) of the Env protein. Such interactions could in principle be used to develop ligands usable for the detection and quantification of a nutrient transporter. Yet, the limited knowledge on the potential targets at the human cell surface recognized by the various RBDs has limited until now the development of probes based on this interaction.

The present invention thus relates to the use of ligands derived from the envelope protein, in particular the RDB domain in said protein, of the porcine endogenous retrovirus of type B (PERV-B. RBD ligands) for the detection and quantification of SMVT on the cell surface, and in particular for diagnostic purposes.

SUMMARY

The present invention relates to an in vitro method for detecting and/or measuring the level of sodium-dependent multivitamin transporter (SMVT) in a biological sample, wherein said method comprises the steps of: a. contacting said biological sample with a PERV-B.RBD ligand, a variant and/or a fragment thereof; and,

b. detecting and/or measuring the binding of said PERV-B.RBD ligand, vari ant and/or fragment thereof to SMVT. In one embodiment, the method of the invention further comprises comparing the binding level measured at step b. with a reference value.

In one embodiment, the amino acid sequence of said PERV-B.RBD ligand, variant and/or fragment thereof comprises or consists of an amino acid sequence selected from the group comprising or consisting of the amino acid sequences SEQ ID NO: 2, SEQ ID, NO: 4, SEQ ID NO: 5, SEQ ID NO:6, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21 and SEQ ID NO: 22 and variants and/or fragments thereof.

In one embodiment, the amino acid sequence of said PERV-B.RBD ligand, variant and/or fragment thereof compri ses or consi sts of an amino acid sequence selected from the group comprising or consisting of the amino acid sequences SEQ ID NO: 2, SEQ ID, NO: 4, SEQ ID NO: 5, SEQ ID NO:6, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 25 and SEQ ID NO: 26 and variants and/or fragments thereof.

In one embodiment, the amino acid sequence of said PERV-B.RBD ligand, variant and/or fragment thereof comprises or consists of an amino acid sequence selected from the group comprising or consisting of the amino acid sequences SEQ ID NO: 5, SEQ ID NO:6, SEQ

ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21 and SEQ ID NO: 22 and variants and/or fragments thereof.

In one embodiment, said PERV-B.RBD ligand, variant and/or fragment thereof is labeled with a detectable label. In one embodiment, said method is for diagnosing a SMVT -related disease in a subject or for identifying a subject as being at risk of developing a SMVT -related disease.

In one embodiment, said SMVT -related disease is cancer, preferably selected from the group comprising liver cancer, prostate cancer, lung, cancer, gallbladder cancer, pancreas cancer, colon cancer, ovarian cancer, brain cancer, kidney cancer, thyroid cancer and lymphomas.

In one embodiment, said SMVT -related disease is a neurodegenerative disease, preferably multiple sclerosis or Huntington’s disease. In one embodiment, said SMVT -related disease is a neuroinflammatory disease, preferably multiple sclerosis.

In one embodiment, said SMVT -related disease is a disorder of pregnancy, preferably pre-eclampsia or intrauterine growth retardation.

In one embodiment, said SMVT -related disease is an infectious disease, preferably an infectious disease caused by a bacterium, more preferably an infectious disease caused by a bacterium belonging to the order Enterobacteriales.

The present invention further relates to a PERV-B.RBD ligand, a variant and/or a fragment thereof for use in an in vivo diagnosis method of a SMVT -related disease in a subject. In one embodiment, said SMVT -related disease is a cancer, a neuroinflammatory or neurodegenerative disease, an infectious disease, a disorder of pregnancy or a disorder related to a mutation in the SLC5A6 gene. In one embodiment, said SMVT -related disease is a cancer, a neuroinflammatory disease, an infectious disease or a disorder of pregnancy. In one embodiment, said SMVT -related disease is a disorder related to a mutation in the SLC5A6 gene. In one embodiment, the SMVT -related disease is cancer, a disorder of pregnancy, an infectious disease or a neurodegenerative disease.

In one embodiment, said cancer is selected from the group comprising or consisting of liver cancer, prostate cancer, lung cancer, gallbladder cancer, pancreas cancer, colon cancer, ovarian cancer, brain cancer, kidney cancer, thyroid cancer, lymphomas, urothelial cancer, cervical cancer and endometrial cancer

In one embodiment, said in vivo diagnosis method is based on medical imaging. The present invention further relates to a PERV-B.RBD ligand coupled to a detectable label, preferably wherein said detectable label is a Fc fragment.

The present invention further relates to the use of the labeled PERV-B.RBD as described herein as a probe for medical imagery.

DEFINITIONS

In the present invention, the following terms have the following meanings:

The term“about” preceding a figure means plus or less 10% of the value of said figure. It is to be understood that the figure to which the term“about” refers is itself also specifically, and preferably, disclosed.

The term“amino acid” as used herein, refers to both natural and synthetic amino acids, and both D and L amino acids. They are represented by their full name, their three letter code or their one letter code as well known in the art. Amino acid residues in peptides are abbreviated as follows: Phenylalanine is Phe or F; Leucine is Leu or L; Isoleucine is lie or I; Methionine is Met or M; Valine is Val or V; Serine is Ser or S; Proline is Pro or P; Threonine is Thr or T; Alanine is Ala or A; Tyrosine is Tyr or Y; Elistidine is His or H; Glutamine is Gln or Q; Asparagine is Asn or N; Lysine is Lys or K; Aspartic Acid is Asp or D; Glutamic Acid is Glu or E; Cysteine is Cys or C; Tryptophan is Trp or W; Arginine is Arg or R; and Glycine is Gly or G.“Standard amino acid” or“naturally occurring amino acid” means any of the twenty standard L-amino acids commonly found in naturally occurring peptides.“Nonstandard amino acid residue” means any amino acid, other than the standard amino acids, regardless of whether it is prepared synthetically or derived from a natural source. For example, naphtlylalanine can be substituted for tryptophan to facilitate synthesis. Other synthetic amino acids that can be substituted include, but are not limited to, L-hydroxypropyl, L-3 ,4-dihydroxyphenyl alanyl , alpha-amino acids such as L-alpha-hydroxylysyl and D-alpha-methylalanyl, L-alpha-methylalanyl, beta-amino acids, and isoquinolyl. The term“amino acid” also encompasses chemically modified amino acids, including, but not limited to, salts, amino acid derivatives (such as amides), and substitutions. Amino acids contained within the polypeptides of the present invention, and particularly at the carboxy- or amino-terminus, can be modified by methylation, amidation, acetylation or substitution with other chemical groups which can change the polypeptide's circulating half-life without adversely affecting their activity. Additionally, a disulfide linkage may be present or absent in the polypeptides of the invention. The RBD ligan ds of the invention may comprise standard amino acids or non-standard amino acids. Polypeptide mimetics include polypeptides having the following modifications: i) polypeptides wherein one or more of the peptidyl -C(0)NR- linkages (bonds) have been replaced by a non-peptidyl linkage such as a -CFb-carbamate linkage (-CH ₂ OC(0)NR-), a phosphonate linkage, a -CFb-sulfonamide (-CH2-S(0)2NR-) linkage, a urea (- NHC(O)NH-) linkage, a -CFb-secondary amine linkage, or with an alkylated peptidyl linkage (-C(O)NR-) wherein R is C1-C4 alkyl; ii) polypeptides wherein the N-terminus is derivatized to a -NRR ¹ group, to a -NRC(0)R group, to a -NRC(0)OR group, to a - NRS(0) ₂ R group, to a -NHC(0)NHR group where R and R ¹ are hydrogen or C1-C4 alkyl with the proviso that R and R ¹ are not both hydrogen; iii) polypeptides wherein the C terminus is derivatized to -C(0)R ² where R ² is selected from the group consisting of Ci-

C4 alkoxy, and -NR ³ R ⁴ where R ³ and R ⁴ are independently selected from the group consisting of hydrogen and C1-C4 alkyl.

The term“cancer”, as used herein, refers to any member of a class of diseases or disorders characterized by uncontrolled division of cells and the ability of these cells to invade other tissues, either by direct growth into adjacent tissue through invasion or by implantation into distant sites by metastasis. Metastasis is defined as the stage in which cancer cells are transported through the bloodstream or lymphatic system. Cancers are classified by the type of cells that the tumor resembles and, therefore, the tissue presumed to be the origin of the tumor. For example, carcinomas are malignant tumors derived from epithelial cells. This group represents the most common cancers, including the common forms of breast, prostate, lung, and colon cancer. Lymphomas and leukemias include malignant tumors derived from blood and bone marrow cells. Sarcomas are malignant tumors derived from connective tissue or mesenchymal cells. Mesotheliomas are tumors derived from the mesothelial cells lining the peritoneum and the pleura. Gliomas are tumors derived from glia, the most common type of brain cell. Germinomas are tumors derived from germ cells, normally found in the testicle and ovary. Choriocarcinomas are malignant tumors derived from the placenta.

The term“diagnosis” as used herein, refers to medical diagnosis, the process of determining which disease explain the symptoms of a subject.

The term“diagnostic composition” refers to a composition to be administered in a subject in order to perform a diagnosis and in particular an in vivo diagnosis. In one embodiment, a diagnostic composition is for detecting cells wherein the function of a vitamin transporter, in particular SMVT, is dysregulated, preferably within the body of a subject.

The term“envelope protein” (“Env”, encoded by the env gene) refers to a protein synthesized as a single polyprotein, which is subsequently cleaved by a cellular furin-like

PR domain into two components: the surface envelope protein (“SU protein” or gp70) and the transmembrane envelope protein (“TM protein” or pl5E). The Env protein is glycosylated. The SU protein is responsible for binding with the host receptor. It comprises a receptor-binding domain (“RBD”). The TM protein, located inside the lipid bilayer anchors the SU protein to the surface of viral particles. The TM protein mediates the membrane fusion reaction with the host cell.

The term“identity”, when used in a relationship between the sequences of two or more polypeptides or of two or more DNA sequences, refers to the degree of sequence relatedness between polypeptides or DNA sequences (respectively), as determined by the number of matches between strings of two or more amino acid residues or of two or more nucleotides, respectively.“Identity” measures the percent of identical matches between the smaller of two or more sequences with gap alignments (if any) addressed by a particular mathematical model or computer program

(/. _<? .,“algorithms”). Identity of related polypeptides or DNA sequences can be readily calculated by known methods. Such methods include, but are not limited to, those described in Arthur M. Lesk, Computational Molecular Biology: Sources and Methods for Sequence Analysis (New- York: Oxford University Press, 1988); Douglas W. Smith, Biocomputing: Informatics and Genome Projects (New- York: Academic Press, 1993); Hugh G. Griffin and Annette M. Griffin, Computer Analysis of Sequence Data, Part 1 (New Jersey: Humana Press, 1994); Gunnar von Heinje, Sequence Analysis in Molecular Biology: Treasure Trove or Trivial Pursuit (Academic Press, 1987); Michael Gribskov and John Devereux, Sequence Analysis Primer (New

York: M. Stockton Press, 1991); and Carillo et al., 1988. SIAM J. Appl. Math. 48(5): 1073-1082. Preferred methods for determining identity are designed to give the l argest match between the sequences tested. Methods of determining identity are described in publicly available computer programs. Preferred computer program methods for determining identity between two sequences include the GCG program package, including GAP (Devereux et al., 1984. Nucl. Acid. Res. 12(1 Pt l):387-395; Genetics Computer Group, University of Wisconsin Biotechnology Center, Madison, WI), BLASTP, BLASTN, TBLASTN and FASTA (Altschul et al., 1990. J. Mol. Biol. 215(3):403-4l0). The BLASTX program is publicly available from the National Center for Biotechnology Information (NCBI) and other sources (BLAST Manual, Altschul et al. NCB/NLM/NIH Bethesda, Md. 20894; Altschul etal, 1990. J. Mol. Biol. 215(3):403- 410). The well-known Smith Waterman algorithm may also be used to determine identity. The term“ligand” as used herein, refers to a small molecule (including but not limited to proteins, peptides, peptidomimetic compounds and other small molecule compounds) that binds specifically to another molecule.

The term“polypeptide” refers to a linear polymer of amino acids (preferably at least 50 amino acids) linked together by peptide bonds.

The terms“porcine endogenous retrovirus” and“PERV” refers to endogenous viruses that belong to the Ortervirales order, Retroviridae family, Orthoretrovirinae subfamily, Gammaretrovirus genus and Porcine type-C oncovirus species (International Committee on the Taxonomy of Viruses - ICTV; Krupovic et al., J Virol. 2018 May 29;92(l2)). As such, they have a single stranded RNA genome characterized by the presence of reverse transcriptase that allows the production of double stranded DNA, subsequently inserted in the genome of the host cells. The term“endogenous retrovirus” refers to the endogenous viral elements in the genome of a host species that become part of the transmitted genes by the host to its progeny. There are three replication-competent subtypes of PERV: porcine endogenous retrovirus type A (PERV -A), porcine endogenous retrovirus type B (PERV-B) and porcine endogenous retrovirus type C (PERV-C). PERV-A and PERV-B are polytropic, capable of infecting both porcine and human cells.

The term“protein” specifically refers to a functional entity formed of one or more polypeptides, and optionally of non-polypeptides cofactors.

The term“sample”, as used herein, refers to any biological material obtained via suitable methods known to the person skilled in the art from a subject. The sample may be collected in a clinically acceptable manner, e.g., in a way that cells, nucleic acids (such as DNA and RNA), proteins and/or metabolites are preserved. A“sample” may include body tissue and/or bodily fluids.

The terms“sodium-dependent multivitamin transporter”,“SMVT”,“solute carrier family

5 member 6” and“SLC5A6” refers to a transmembrane protein present at the surface of cells in several organisms including, but not limited to, drosophila, zebrafish, rodents, pig, primates and human. SMVT belong to the group of solute carrier membrane transport protein that comprises over 400 identified members organized into 65 families. SMVT, like most member of the SLC group, is located in the plasma membrane where it is responsible for sodium-dependent uptake of biotin, pantothenic acid and lipoic acid. The protein bears 12 transmembrane domains with both amino and carboxyl termini predicted to be located on the cytoplasmic side. In human, the SMVT protein is the product of the SLC5A6 gene. SLC5A6 is expressed in various tissues including, but not limited to, placenta, intestine, brain, liver, lung, kidney, cornea, retina and heart. The modification of the level of SMVT, beyond reflecting the metabolic state of a cell, has also been associated with several diseases.

The term“SMVT -related diseases” refers to diseases associated with a modification (e.g., an overexpression or down-expression) of the level of SMVT at the surface of a subject cells. The term thus encompasses diseases associated with a deregulation of biotin, pantothenic acid and lipoid acid uptake such as for example embryonic growth retardation, neurological disorders and dermatological disorders. Furthermore, a variation of the expression of SMVT has been found associated with cancer, in particular liver cancer, prostate cancer, lung cancer, gallbladder cancer, pancreas cancer, colon cancer, ovarian cancer, brain cancer, kidney cancer and lymphomas. The term“therapeutically effective amount” means level or amount of agent that is aimed at, without causing significant negative or adverse side effects to the target, (1) delaying or preventing the onset of a SMVT -related disease; (2) slowing down or stopping the progression, aggravation, or deterioration of one or more symptoms of a SMVT -related disease; (3) bringing about ameliorations of the symptoms of a SMVT- related disease; (4) reducing the severity or incidence of a SMVT -related disease; or (5) curing a SMVT -related disease. A therapeutically effective amount may be administered prior to the onset of a SMVT -related disease, for a prophylactic or preventive action. Alternatively or additionally, the therapeutically effective amount may be administered after initiation of a SMVT -related disease, for a therapeutic action.

The term“treatment” refers to both therapeutic treatment and prophylactic or preventive measures; wherein the object is to prevent or slow down (lessen) a SMVT -related disease. Those in need of treatment include those already with a SMVT -related disease as well as those prone to have a SMVT -related disease or those in whom a SMVT -related disease is to be prevented. A subject or mammal is successfully“treated” for a disease if, after receiving a therapeutic amount of a ligand according to the invention, the patient shows observable and/or measurable reduction in or absence of one or more of the following: reduction in the number of pathogenic cells; reduction in the percentage of total cells that are pathogenic; and/or relief to some extent, of one or more of the symptoms associated with the specific disease or condition; reduced morbidity and mortality, and improvement in quality of life issues. The above parameters for assessing successful treatment and improvement in the disease are readily measurable by routine procedures familiar to a physician.

The term“subject”, as used herein, refers to an animal, preferably a mammal, more preferably a human. In one embodiment, the subject is a patient, i.e., a recipient of health care services, who/which is awaiting the receipt of, or is receiving medical care or was/is/will be the object of a medical procedure, or is monitored for the development of a disease.

The term“variant” refers to a polypeptide variant that typically differs from a polypeptide specifically disclosed herein in one or more substitutions, deletions, additions and/or insertions. Such variants may be naturally occurring or may be synthetically generated, for example, by modifying one or more of the above polypeptide sequences and evaluating one or more biological activities of the polypeptide as described herein and/or using any of a number of techniques well known in the art. Modifications may be made in the structure of polypeptides and still obtain a functional molecule that encodes a variant or derivative polypeptide with desirable characteristics. When it is desired to alter the amino acid sequence of a polypeptide to create an equivalent, or even an improved, variant or portion of a ligand of the invention, one skilled in the art will typically change one or more of the codons of the encoding DNA sequence. For example, certain amino acids may be substituted by other amino acids in a protein structure without appreciable loss of its ability to bind to a cell surface receptor, preferably to cell surface nutrient transporters, more preferably to SMVT. Since it is the binding capacity and nature of a protein that defines that protein’s biological functional activity, certain amino acid sequence substitutions can be made in a protein sequence, and, of course, its underlying DNA coding sequence, and nevertheless obtain a protein with similar properties. It is thus contemplated that various changes may be made in the peptide sequences, or corresponding DNA sequences that encode said peptides without appreciable loss of their biological utility or activity. In many instances, a polypeptide variant will contain one or more conservative substitutions. A“conservative substitution” is one in which an amino acid is substituted by another amino acid that has similar properties, such that one skilled in the art of peptide chemistry would expect the secondary structure and hydropathic nature of the polypeptide to be substantially unchanged. As outlined above, amino acid substitutions are generally therefore based on the relative similarity of the amino acid side-chain substituents, for example, their hydrophobicity, hydrophilicity, charge, size, and the like. Exemplary substitutions that take various of the foregoing characteristics into consideration are well known to those of skilled in the art and may include substitution within the following groups: arginine and lysine; glutamate and aspartate; serine and threonine; glutamine and asparagine; and valine, leucine and isoleucine. Amino acid substitutions may further be made on the basis of similarity in polarity, charge, solubility, hydrophobicity, hydrophilicity and/or the amphipathic nature of the residues. For example, negatively charged amino acids include aspartic acid and glutamic acid; positively charged amino acids include histidine, lysine and arginine; and amino acids with uncharged polar head groups having similar hydrophilicity values include leucine, isoleucine and valine; glycine and alanine; asparagine and glutamine; and, serine, threonine, phenylalanine and tyrosine. Other groups of amino acids that may represent conservative changes include: (1) Ala, Pro, Gly, Glu, Asp, Gln, Asn, Ser, Thr; (2) Cys, Ser, Tyr, Thr; (3) Yal, Ile, Leu, Met, Ala, Phe; (4) Lys, Arg, His; and (5) Phe, Tyr, Trp, His. The term“conservative amino acid substitution” may further be defined as an amino acid exchange within one of the following five groups: I: Small aliphatic, nonpolar or slightly polar residues: Ala, Ser, Thr, Pro, Gly; II: Polar, negatively charged residues and their amides: Asp, Asn, Glu, Gln; III: Polar, positively charged residues: His, Arg, Lys; IV: Large, aliphatic, nonpolar residues: Met, Leu, Ile, Val, Cys; V. Large, aromatic residues: Phe, Tyr, Trp. A variant may also, or alternatively, contain non-conservative changes. In a preferred embodiment, variant polypeptides differ from a native sequence by substitution, deletion or addition of 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 amino acids. Variants may also (or alternatively) be modified by, for example, the deletion or addition of amino acids that have minimal influence on the immunogenicity, secondary structure, hydropathic nature and/or binding properties of the polypeptide.

DETAILED DESCRIPTION

The present invention relates to in vitro methods for detecting and/or measuring the level of the cell surface nutrient transporter sodium-dependent multivitamin transporter (SMVT) in a biological sample, wherein said method comprises the steps of:

a. contacting said biological sample with at least one PERV-B.RBD ligand, a variant and/or fragment thereof; and,

b. detecting and/or measuring the binding of said PERV-B.RBD ligand, variant and/or fragment thereof to SMVT.

The present invention relates to in vitro methods for detecting and/or measuring the level of the cell surface nutrient transporter sodium-dependent multivitamin transporter (SMVT) in a biological sample, wherein said method comprises the steps of:

a. contacting said biological sample with at least one PERV-B.RBD ligand, a variant and/or fragment thereof; and, b. measuring the binding of said PERV-B.RBD ligand, variant and/or fragment thereof to SMYT.

As used herein, the term PERV-B.RBD ligand refers to a receptor binding domain (RED) ligand derived from the envelope protein of porcine endogenous retrovirus type B (PERV-B).

In one embodiment, the term“level of SMVT” refers to the amount of SMVT present at the surface of a cell and/or within the cell.

In one embodiment, the method of the invention is for assessing the expression level of SMVT present on the cell surface. In another embodiment, the method of the invention is for assessing the expression level of SMVT present within the cell.

In one embodiment, SMVT is human SMVT (UniProtKB - Q9Y289 - SEQ ID NO: 1).

(SEQ ID NO: 1)

MSVGVSTSAPLSPTSGTSVGMSTFSIMDYVVFVLLLVLSLAIGLYHACRGWGRH TVGELLMADRKMGCLPVALSLLATFQSAVAILGVPSEIYRFGTQYWFLGCCYF LGLLIPAHIFIPVFYRLHLTS AYE YLELRENKTVRVCGT VTFIF QM VIYMGVVL Y

APSLALNAVTGFDLWLSVLALGIVCTVYTALGGLKAVIWTDVFQTLVMFLGQL AVIIVGSAKVGGLGRVWAVASQHGRISGFELDPDPFVRHTFWTLAFGGVFMML SLYGVNQAQVQRYLSSRTEKAAVLSCYAVFPFQQVSLCVGCLIGLVMFAYYQE YPMSIQQAQAAPDQFVLYFVMDLLKGLPGLPGLFIACLFSGSLSTISSAFNSLAT VTMEDLIRPWFPEFSEARAIMLSRGLAFGYGLLCLGMAYISSQMGPVLQAAISIF GMVGGPLLGLFCLGMFFPCANPPGAVVGLLAGLVMAFWIGIGSIVTSMGSSMP PSPSNGSSFSLPTNLTVATVTTLMPLTTFSKPTGLQRFYSLSYLWYSAHNSTTVI VVGLIVSLLTGRMRGRSLNPATIYPVLPKLLSLLPLSCQKRLHCRSYGQDHLDT GLFPEKPRNGVLGDSRDKEAMALDGTAYQGSSSTCILQETSL In one embodiment, SMVT is a human SMVT comprising or consisting of an amino acid sequence SED ID NO: 24. In one embodiment, SMVT comprises or consists of an amino acid sequence presenting a sequence identity of at least about 70% with the amino acid sequence SEQ ID NO: 1, preferably a sequence identity of at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more with the amino acid sequence SEQ ID NO: 1 or 24.

In one embodiment, SMVT comprises or consists of a fragment of SEQ ID NO: 1 or 24, preferably a fragment of at least about 100 amino acids, more preferably of at least about 150, 200, 250, 300, 350, 400, 450, 500, 550, 600 amino acids.

In one embodiment, the PERV-B.RBD ligand of the invention comprises a part or the totality of the receptor-binding domain (RBD) found in the surface component of the envelope protein (Env) of porcine endogenous retrovirus (PERV) that binds SMVT. In one embodiment, the PERV-B.RBD ligand of the invention comprises a part or the totality of the receptor-binding domain (RBD) found in the surface component of the envelope protein (Env) of porcine endogenous retrovirus type B (PERV-B) that binds SMVT.

In one embodiment, the PERV-B.RBD ligand of the invention comprises a part or the totality of the surface envelope protein. In one embodiment PERV-B.RBD ligand of the invention does not comprise the transmembrane domain of the envelope protein. Therefore, in one embodiment, the PERV-B.RBD ligand of the invention is a soluble peptide. As used herein, the term“soluble peptide” refers to a peptide which is not anchored within a membrane, such as, for example, by a transmembrane or a GPI anchor domain.

In one embodiment, the PERV-B.RBD ligand of the invention comprises a part or the totality of the receptor-binding domain (RBD) found in the soluble part of the envelope protein (Env) of porcine endogenous retrovirus-B (PERV-B) that binds to SMVT.

In one embodiment, the envelope protein of PERV-B comprises or consists of a sequence SEQ ID NO: 2 (Uniprot accession number: Q6W4T9 - GenBank Accession number AA Q88198.1), or a sequence presenting a sequence identity of at least about 70%, preferably a sequence identity of at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more, with the amino acid sequence SEQ ID NO: 2.

(SEQ ID NO: 2)

MHPTLSWRHLPTRGGEPKRLRIPLSFASIAWFLTLTITPQASSKRLIDSSNPHRPL SLTWLIIDPDTGVTVNSTRGVAPRGTWWPELHFCLRLINPAVKSTPPNLVRSYG FYCCPGTEKEKYCGGSEESFCRRWSCVTSNDGDWKWPISLQDRVKFSFVNSGP GKYKVMKLYKDKSCSPSDLDYLKISFTEKGKQENIQKWINGMSWGIVFYKYG GGAGSTLTIRLRIETGTEPPVAVGPDKVLAEQGPPALEPPHNLPVPQLTSLRPDIT QPPSNGTTGLIPTNTPRNSPGVPVKTGQRLFSLIQGAFQAINSTDPDATSSCWLC LSSGPPYYEGMAKEGKFNVTKEHRNQCTWGSRNKLTLTEVSGKGTCIGKAPPS HQHLC Y ST V V YEQ ASEN Q YE VPGYNRWWACNT GLPPC V S S S VFN Q SKDF C VM

V QI VPRVYYE1PEEVVLDE YD YRYNRPKREPV SLTLAVMLGLGTAV GV GT GTA ALITGPQQLEKGLGELHAAMTEDLRALEESVSNLEESLTSLSEVVLQNRRGLDL LFLREGGLCAA In another embodiment, the envelope protein of PERV-B comprises or consists of a sequence SEQ ID NO: 17, or a sequence presenting a sequence identity of at least about 70%, preferably a sequence identity of at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more, with the amino acid sequence SEQ ID NO: 17. (SEQ ID NO: 17)

MHPTLSWRHLPTRGGEPKRLRIPLSFASIAWFLTLTITPQASSKRLIDSSNPHRPL SLTWLIIDPDTGVTVNSTRGVAPRGTWWPELHFCLRLINPAVKSTPPNLVRSYG FYCCPGTEKEKYCGGSGESFCRRWSCVTSNDGDWKWPISLQDRVKESFVNSGP GKYKVMKLYKDKSCSPSDLDYLKISFTEKGKQENIQKWINGMSWGIVFYKYG GGAGSTLTIRLRIETGTEPPVAVGPDKVLAEQGPPALEPPHNLPVPQLTSLRPDIT QPPSNGTTGLIPTNTPRNSPGVPVKTGQRLFSLIQGAFQAINSTDPDATSSCWLC LSSGPPYYEGMAKEGKFNVTKEHRNQCTWGSRNKLTLTEVSGKGTCIGKAPPS HQHLC Y ST VV YEQ ASEN QYL VPGYNRWWACNT GLTPC V ST S VFN Q SKDF C YM

V QIYPRVYYHPEEVVLDE YD YRYNRPKREPV SLTLAVMLGLGTAV GY GT GTA ALITGPQQLEKGLGELHAAMTEDLRALEESVSNLEESLTSLSEVVLQNRRGLDL

LFLREGGLCAA

In another embodiment, the envelope protein of PERV-B comprises or consists of a sequence SEQ ID NO: 25, or a sequence presenting a sequence identity of at least about 70%, preferably a sequence identity of at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more, with the amino acid sequence SEQ ID NO: 25.

(SEQ ID NO: 25)

MHPTLSWRHLPTRGGEPKRLRIPLSFASIAWFLTLTITPQASSKRLIDSSNPHRPL

SLTWLIIDPDTGVTVNSTRGVAPRGTWWPELHFCLRLINPAVKSTPPNLVRSYG

FYCCPGTEKEKYCGGSEESFCRRWSCVTSNDGDWKWPISLQDRVKFSFVNSGP

GKYKVMKLYKDKSCSPSDLDYLKISFTEKGKQENIQKWINGMSWGIVFYKYG

GGAGSTLTIRLRIETGTEPPVAVGPDKVLAEQGPPALEPPHNLPVPQLTSLRPDIT

QPPSNGTTGLIPTNTPRNSPGVPVKTGQRLFSLIQGAFQAINSTDPDATSSCWLC

LSSGPPYYEGMAKEGKFNVTKEHRNQCTWGSRNKLTLTEVSGKGTCIGKAPPS

HQHLC Y ST V V YEQ ASEN Q YL VPGYNRWWACNT GLTPC Y S S S VFN Q SKDFC VM

VQIVPRVYYHPEEVVLDEYDYRYNRPKREPVSLTLAVMLGLGTAVGVGTGTA

ALITGPQQLEKGLGELHAAMTEDLRALEESVSNLEESLTSLSEVYLQNRRGLDL

LFLREGGLCAA

In one embodiment, the amino-acid sequence of the PERY-B.RBD ligand of the invention comprises or consists of a fragment of SEQ ID NO: 2, 17 or 25, or a variant thereof.

In one embodiment, the amino-acid sequence of the PERV-B. RBD ligand of the invention comprises or consists of amino acids 1 to 540, preferably 1 to 530, 1 to 520, 1 to 510, 1 to 500, 1 to 490, 1 to 480, 1 to 490, 1 to 480, 1 to 470, 1 to 460, 1 to 450, 1 to 440, 1 to 430, 1 to 420, 1 to 410, 1 to 400, 1 to 390, 1 to 380, 1 to 370, 1 to 360, 1 to 350, 1 to 340, 1 to 330, 1 to 320, 1 to 310, 1 to 300, 1 to 290, 1 to 280, 1 to 270, 1 to 260, 1 to 250, 1 to 240, more preferably 1 to 238 of SEQ ID NO: 2, 17 or 25, or a variant thereof. In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention does not comprise a signal peptide, preferably does not comprise a signal peptide of amino sequence SEQ ID NO: 3 or a sequence presenting a sequence identity of at least about 70%, preferably a sequence identity of at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more, with the amino acid sequence SEQ ID

NO: 3. In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention does not comprise a signal peptide corresponding to the first 38, 39, 40, 41 or 42 amino acids of SEQ ID NO: 3.

(SEQ ID NO: 3) MHPTLSWRHLPTRGGEPKRLRIPLSFASIAWFLTLTITPQASS

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of amino acids 44 to 540, preferably 44 to 530, 44 to 520, 44 to 510, 44 to 500, 44 to 490, 44 to 480, 44 to 470, 44 to 460, 44 to 450, 44 to 440, 44 to 430, 44 to 420, 44 to 410, 44 to 400, 44 to 390, 44 to 380, 44 to 370, 44 to 360, 44 to 350, 44 to 340, 44 to 330, 44 to 320, 44 to 310, 44 to 300, 44 to 290, 44 to 280, 44 to 270, 44 to 260, 44 to 250, 44 to 240, more preferably 44 to 238 of SEQ ID NO: 2, 17 or 25, or variants thereof.

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of amino acids 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 540, preferably 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 530; 39, 40, 41, 42, 43, 44, 45,

46, 47, 48 or 49 to 520; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 510; 39, 40, 41, 42,

43, 44, 45, 46, 47, 48 or 49 to 500; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 490; 39,

40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 480; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 470, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 460; 39, 40, 41, 42, 43, 44, 45, 46,

47, 48 or 49 to 450; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 440; 39, 40, 41, 42, 43,

44, 45, 46, 47, 48 or 49 to 430; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 420; 39, 40,

41, 42, 43, 44, 45, 46, 47, 48 or 49 to 410; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 400; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 390; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 380; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 370; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 360; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 350; 39, 40, 41,

42, 43, 44, 45, 46, 47, 48 or 49 to 340; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 330;

39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 320; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or

49 to 310; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 300; 39, 40, 41, 42, 43, 44, 45,

46, 47, 48 or 49 to 290; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 280; 39, 40, 41, 42,

43, 44, 45, 46, 47, 48 or 49 to 270; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 260; 39,

40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 250; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 240; more preferably 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 238 of SEQ ID NO: 2, 17 or 25, or variants thereof. In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of an amino acid sequence presenting a sequence identity of at least about 70%, preferably a sequence identity of at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more, with the amino acid sequence SEQ ID NO: 2, 17 or 25, a variant and/or a fragment thereof. In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of the amino acid sequence of an SU domain of the Env protein of porcine endogenous retrovirus-B (SEQ ID NO: 4), a variant and/or a fragment thereof.

(SEQ ID NO: 4)

MHPTLSWRHLPTRGGEPKRLRIPLSFASIAWFLTLTITPQASSKRLIDSSNPHRPL SLTWLIIDPDTGVTVNSTRGVAPRGTWWPELHFCLRLINPAVKSTPPNRVRSYG FYCCPGTEKEKYCGGSEESFCRRWSCVTSNDGDWKWPISEQDRVKFSFVNSGP GKYKVMKLYKDKSCSPSDLDYLKISFTEKGKQENIQKWINGMSWGIVFYKYG GGAGSTLTIRLRIETGTEPPVAVGPDKVLAEQGPPAEEPPHNLPVPQLTSERPDIT QPPSNGTTGLIPTNTPRNSPGVPVKTGQRLFSLIQGAFQAINSTDPDATSSCWFC LSSGPPYYEGMAKEGKFNVTKEHRNQCTWGSRNKLTLTEVSGKGTCIGKAPPS HQHECYSTVVYEQASENQYEVPGYNRWWACNTGEPPCVSSSVFNQSKDFCVM V QI VPRV Y YHPEE V VLDE YD YRYNRPKR In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of the amino acid sequence of an SU domain of the Env protein of porcine endogenous retro virus-B (SEQ ID NO: 18), a variant and/or a fragment thereof.

(SEQ ID NO: 18) MHPTLSWRHLPTRGGEPKRLRIPLSFASIAWFLTLTITPQASSKRLIDSSNPHRPL

SLTWLIIDPDTGVTVNSTRGVAPRGTWWPELHFCLRLINPAVKSTPPNLVRSYG FYCCPGTEKEKYCGGSGESFCRRWSCVTSNDGDWKWPISLQDRVKFSFVNSGP GKYKVMKE YKDKS C SP SDLD YLKI SFTEKGKQENIQKWIN GMS WGI VF YKY G GGAGSTLTIRLRIETGTEPPVAVGPDKVLAEQGPPALEPPHNLPVPQLTSLRPDIT QPPSNGTTGLIPTNTPRNSPGVPVKTGQRLFSLIQGAFQAINSTDPDATSSCWLC LSSGPPYYEGMAKEGKFNVTKEHRNQCTWGSRNKLTLTEVSGKGTCIGKAPPS HQHLC Y ST V V YEQ ASEN Q YL VPGYNRWWACNT GLTPC V ST S VFN Q SKDF C VM V QI VPRV Y YHPEE V VLDE YD YRYNRPKR

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of the amino acid sequence of an SU domain of the Env protein of porcine endogenous retro virus-B (SEQ ID NO: 26), a variant and/or a fragment thereof.

(SEQ ID NO: 26)

MHPTLSWRHLPTRGGEPKRLRIPLSFASIAWFLTLTITPQASSKRLIDSSNPHRPL SLTWLIIDPDTGVTVNSTRGVAPRGTWWPELHFCLRLINPAVKSTPPNLVRSYG FYCCPGTEKEKYCGGSEESFCRRWSCVTSNDGDWKWPISLQDRVKFSFVNSGP GKYKVMKL YKDKS C SP SDLD YLKI SFTEKGKQENIQKWIN GMS WGI VF YKY G GGAGSTLTIRLRIETGTEPPVAVGPDKVLAEQGPPALEPPHNLPVPQLTSLRPDIT QPPSNGTT GLIPTNTPRNSPGVP VKT GQRLFSLIQGAF Q AINSTDPD ATS SC WLC LSSGPPYYEGMAKEGKFNVTKEHRNQCTWGSRNKLTLTEVSGKGTCIGKAPPS HQHLC Y ST VV YEQ ASEN QYL VPGYNRWWACNT GLTPC V S S S VFN Q SKDFC VM VQIVPRVYYHPEEVVLDEYD YRYNRPKR

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of amino acids 1 to 480, preferably of 1 to 470, 1 to 460, 1 to 450, 1 to 440, 1 to 430, 1 to 420, 1 to 410, 1 to 400, 1 to 390, 1 to 380, 1 to 370, 1 to 360, 1 to 350, 1 to 340, 1 to 330, 1 to 320, 1 to 310, 1 to 300, 1 to 290, 1 to 280, 1 to 270, 1 to 260, 1 to 250, 1 to 240, more preferably 1 to 238 of SEQ ID NO: 4, 18 or 26, or a variant thereof.

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of amino acids 44 to 480, preferably of 44 to 470, 44 to 460, 44 to 450, 44 to 440, 44 to 430, 44 to 420, 44 to 410, 44 to 400, 44 to 390, 44 to 380, 44 to 370, 44 to 360, 44 to 350, 44 to 340, 44 to 330, 44 to 320, 44 to 310, 44 to 300, 44 to 290, 44 to 280, 44 to 270, 44 to 260, 44 to 250, 44 to 240, more preferably 44 to 238 of SEQ ID NO: 4, 18 or 26, or a variant thereof.

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of amino acids 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 480; preferably of 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 470; 39, 40, 41, 42, 43, 44, 45,

46, 47, 48 or 49 to 460; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 450; 39, 40, 41, 42,

43, 44, 45, 46, 47, 48 or 49 to 440; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 430; 39,

40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 420; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 410; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 400; 39, 40, 41, 42, 43, 44, 45, 46,

47, 48 or 49 to 390; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 380; 39, 40, 41, 42, 43,

44, 45, 46, 47, 48 or 49 to 370; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 360; 39, 40,

41, 42, 43, 44, 45, 46, 47, 48 or 49 to 350; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 340; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 330; 39, 40, 41, 42, 43, 44, 45, 46, 47,

48 or 49 to 320; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 310; 39, 40, 41, 42, 43, 44,

45, 46, 47, 48 or 49 to 300; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 290; 39, 40, 41,

42, 43, 44, 45, 46, 47, 48 or 49 to 280; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 270;

39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 260; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or

49 to 250; 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 240; more preferably 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 238 of SEQ ID NO: 4, 18 or 26, or a variant thereof.

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of an amino acid sequence presenting a sequence identity of at least about 70%, preferably a sequence identity of at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more, with the amino acid sequence SEQ ID NO: 4, 18 or 26, a variant and/or a fragment thereof.

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of the amino acid sequence SEQ ID NO: 5, a variant and/or a fragment thereof.

(SEQ ID NO: 5)

MHPTLSWRHLPTRGGEPKRLRIPLSFASIAWFLTLTITPQASSKRLIDSSNPHRPL

SLTWLIIDPDTGVTVNSTRGVAPRGTWWPELHFCLRLINPAVKSTPPNLVRSYG

FYCCPGTEKEKYCGGSEESFCRRWSCVTSNDGDWKWPISLQDRVKFSFVNSGP GKYKVMKLYKDKSCSPSDLD YLKISFTEKGKQENIQKWINGMSWGIVFYKYG

GGAGSTLTIRLRIEAGTEPPYAV

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of the amino acid sequence SEQ ID NO: 19, a variant and/or fragment thereof. (SEQ ID NO: 19)

MHPTLSWRHLPTRGGEPKRLRIPLSFASIAWFLTLTITPQASSKRLIDSSNPHRPL SLTWLIIDPDT GVT VNSTRGVAPRGT WWPELHF CLRLINPAVKSTPPNLVRS Y G FYCCPGTEKEKYCGGSGESFCRRWSCVTSNDGDWKWPISLQDRVKFSFVNSGP GKYKVMKLYKDKSCSPSDLD YLKISFTEKGKQENIQKWINGMSWGIVFYKYG GG AGSTLTIRLRIET GTEPP VAV

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of the amino acid sequence SEQ ID NO: 21, a variant and/or a fragment thereof.

(SEQ ID NO: 21) MHPTLSWRHLPTRGGEPKRLRIPLSFASIAWFLTLTITPQASSKRLIDSSNPHRPL SLTWLIIDPDTGVTVNSTRGVAPRGTWWPELHFCLRLINPAVKSTPPNLVRSYG FYCCPGTEKEKYCGGSEESFCRRWSCVTSNDGDWKWPISLQDRVKFSFVNSGP GKYKVMKL YKDKS C SP SDLD YLKI SFTEKGKQENIQKWIN GMS WGI VF YKY G GG AGSTLTIRLRIET GTEPP YAV

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention compri ses or consists of an amino acid sequence presenting a sequence identity of at least about 70%, preferably a sequence identity of at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more, with the amino acid sequence SEQ ID NO: 5, 19 or 21, a variant and/or a fragment thereof.

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of amino acids 44 to 238 of SEQ ID NO: 5, 19 or 21, or a variant thereof.

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of amino acids 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 238 of SEQ ID NO: 5, 19 or 21, or a variant thereof.

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of the amino acid sequence SEQ ID NO: 6, a variant and/or a fragment thereof.

(SEQ ID NO: 6)

KRLIDSSNPHRPLSLTWLIIDPDTGVTVNSTRGVAPRGTWWPELHFCLRLINPAV KSTPPNLVRS Y GFY CCPGTEKEKY CGGSEESFCRRW SC VTSNDGDWKWPISLQ DRVKFSFVNSGPGKYKVMKLYKDKSCSPSDLDYLKISFTEKGKQEN1QKWING MSWGIVFYKYGGGAGSTLTIRLRIEAGTEPPVAV

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of the amino acid sequence SEQ ID NO: 20, a variant and/or a fragment thereof. (SEQ ID NO: 20)

KRLIDS SNPHRPLSLTWLIIDPDT GVTVN STRGVAPRGTWWPELHFCLRLINPAV

KSTPPNLVRSYGFYCCPGTEKEKYCGGSGESFCRRWSCYTSNDGDWKWPISLQ DRVKFSFVNSGPGKYKVMKLYKDKSCSPSDLDYLKISFTEKGKQENIQKWING MSWGIVFYKYGGGTGSTLTIRLRIETGTEPPVAV

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of the amino acid sequence SEQ ID NO: 22, a variant and/or a fragment thereof.

(SEQ ID NO: 22) KRLIDSSNPHRPLSLTWLIIDPDTGVTVNSTRGVAPRGTWWPELHFCLRLINPAV KSTPPNLVRS Y GFY CCPGTEKEKY CGGSEESFCRRW SC VTSNDGDWKWPISLQ DRVKFSFVNSGPGKYKYMKLYKDKSCSPSDLDYLKISFTEKGKQENIQKWING MSWGIVFYKYGGGAGSTLTIRLRIETGTEPPVAV

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of amino acids 2, 3, 4, 5, or 6 to 195 of SEQ ID NO: 6, 20 or 22, or a variant thereof.

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of amino acids 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 238 of SEQ ID NO: 2, 17, 25, 4, 18, 26, 5, 19 or 21, or a variant thereof. In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of an amino acid sequence presenting a sequence identity of at least about 70%, preferably a sequence identity of at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more, with the amino acid sequence SEQ ID NO: 6, 20 or 22, a variant and/or a fragment thereof. In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of an amino acid sequence presenting a sequence identity of at least about 70%, preferably a sequence identity of at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more, with the amino acid sequence SEQ ID NO: 5, 19 or 21, a variant and/or a fragment thereof.

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of the amino acid sequence selected from the group comprising or consisting of the amino acid sequences SEQ ID NO: 2, 4, 5, 6, 17, 18, 19, 20, 21 and 22 and, variants and/or fragments thereof.

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of the amino acid sequence selected from the group comprising or consisting of the amino acid sequences SEQ ID NO: 2, 4, 5, 6, 17, 18, 19, 20, 21, 22, 25 and 26, variants and/or fragments thereof.

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of an amino acid sequence presenting a sequence identity of at least about 70%, preferably a sequence identity of at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more, with an amino acid sequence selected from the group comprising or consisting of the amino acid sequences SEQ ID NO: 2, 4, 5, 6, 17, 18, 19, 20, 21 and 22 and, variants and/or fragments thereof.

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of an amino acid sequence presenting a sequence identity of at least about 70%, preferably a sequence identity of at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more, with an amino acid sequence selected from the group comprising or consisting of the amino acid sequences SEQ ID NO: 2, 4, 5, 6, 17, 18, 19, 20, 21, 22, 25 and 26 and, variants and/or fragments thereof.

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of the amino acid sequence sel ected from the group comprising or consisting of the amino acid sequences SEQ ID NO: 5, 6, 19, 20, 21 and 22 and, variants and/or fragments thereof.

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention comprises or consists of the amino acid sequence selected from the group comprising or consisting of the amino acid sequences SEQ ID NO: 5, 19, and 21 and, variants and/or fragments thereof.

In one embodiment, the nucleic acid sequence encoding the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, comprises or consists of the nucleic acid sequence SEQ ID NO: 7, a variant and/or a fragment thereof.

(SEQ ID NO: 7)

AT GC ATCCC ACGTTAAGCTGGCGCC ACCTCCCGACTCGGGGT GGAGAGCCG AAAAGACTGAGAATCCCCTTAAGCTTCGCCTCCATCGCCTGGTTCCTTACTC TAACAATAACTCCCCAGGCCAGTAGTAAACGCCTTATAGACAGCTCGAACC CCCATAGACCTTTATCCCTTACCTGGCTGATTATTGACCCTGATACGGGTGT C ACT GT AAAT AGC ACT C G AGGT GTT GCTCCT AG AGGC ACCT GGT GGCCT G A ACTGCATTTCTGCCTCCGATTGATTAACCCCGCTGTTAAAAGCACACCTCCC AACCT AGT C CGT AGTT AT GGGTT CT ATT GCT GCC C AGGC AC AG AG AAAG AG AAATACTGTGGGGGTTCTGAGGAATCCTTCTGTAGGAGATGGAGCTGCGTC ACCTCCAACGATGGAGACTGGAAATGGCCGATCTCTCTCCAGGACCGGGTA AAATTCTCCTTTGTCAATTCCGGCCCGGGCAAGTACAAAGTGATGAAACTAT AT AAAG AT AAG AGCT GCT CC CC ATC AG ACTT AG ATT AT CT AAAG AT AAGTTT C ACT GAAAAAGGAAAAC AGGAAAATATTCAAAAGT GGATAAATGGTATGA GCTGGGGAATAGTTTTTTATAAATATGGCGGGGGAGCAGGGTCCACTTTAA CCATTCGCCTTAGGATAGAGGCGGGGACAGAACCCCCTGTGGCAGTG

In one embodiment, the nucleic acid sequence encoding the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, comprises or consists of a nucleic acid sequence presenting a sequence identity of at least about 70%, preferably a sequence identity of at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more, with the nucleic acid sequence SEQ ID NO: 7, a variant and/or a fragment thereof.

In one embodiment, the nucleic acid sequence encoding the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, comprises or consists of the nucleic acid sequence SEQ ID NO: 8, a variant and/or a fragment thereof. (SEQ ID NO: 8)

AAACGCCTTATAGACAGCTCGAACCCCCATAGACCTTTATCCCTTACCTGGC

T GATT ATT G AC CCT GAT ACGGGT GT C ACT GT AAAT AGC ACT C G AGGT GTTGC TCCT AGAGGC ACCT GGT GGCCT GAACT GC ATTT CT GCCTCCGATT GATTAAC CCCGCTGTTAAAAGCACACCTCCCAACCTAGTCCGTAGTTATGGGTTCTATT GCTGC CC AGGC AC AG AG AA AG AGAAAT ACT GT GGGG GTT CT G AGG AATCCT TCTGTAGGAGATGGAGCTGCGTCACCTCCAACGATGGAGACTGGAAATGGC CGATCTCTCTCCAGGACCGGGTAAAATTCTCCTTTGTCAATTCCGGCCCGGG CAAGTACAAAGTGATGAAACTATATAAAGATAAGAGCTGCTCCCCATCAGA CTT AG ATT AT CT AAAG AT AAGTTT C ACT G AAAAAGG AAAAC AGG AAAAT AT T CAAAAGTGGATAAAT GGTATGAGCT GGGGAATAGTTTTTTATAAATAT GG C GGGGG AGC AGGGT C C ACTTT AACC ATTCGC CTT AGG AT AGAGGC GGGG AC AGAACCCCCTGTGGCAGTG

In one embodiment, the nucleic acid sequence encoding the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, comprises or consists of a nucleic acid sequence presenting a sequence identity of at least 70%, preferably a sequence identity of at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more, with the nucleic acid sequence SEQ ID NO: 8, a variant and/or a fragment thereof. In one embodiment, the nucleic acid sequence encoding the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, comprises or consists of the nucleic acid sequence SEQ ID NO: 27, a variant and/or a fragment thereof.

(SEQ ID NO: 27)

AT GC ATCCC ACGTTAAGCTGGCGCC ACCTCCCGACTCGGGGT GGAGAGCCG AAAAGACTGAGAATCCCCTTAAGCTTCGCCTCCATCGCCTGGTTCCTTACTC TAACAATAACTCCCCAGGCCAGTAGTAAACGCCTTATAGACAGCTCGAACC CCCATAGACCTTTATCCCTTACCTGGCTGATTATTGACCCTGATACGGGTGT C ACT GTAAAT AGC ACTCGAGGT GTT GCTCCT AGAGGC ACCT GGT GGCCT GA ACTGCATTTCTGCCTCCGATTGATTAACCCCGCTGTTAAAAGCACACCTCCC AACCT AGT C CGT AGTT AT GGGTT CT ATT GCT GCC C AGGC AC AG AG AAAG AG

AAATACTGT GGGGGTT CT GAGGAATCCTTCT GT AGGAGATGGAGCT GCGT C ACCTCCAACGATGGAGACTGGAAATGGCCGATCTCTCTCCAGGACCGGGTA AAATT CTCCTTT GT CAATTCCGGCCCGGGC AAGTAC AAAGT GATGAAACTAT AT AAAG AT AAG AGCT GCTCC CC AT C AG ACTT AG ATT AT CT AAAG AT AAGTTT C ACT G AAAAAGGAAAAC AGG AAAAT ATT C AAAAGT GG AT AAAT GGT AT G A GCTGGGGAATAGTTTTTTATAAATATGGCGGGGGAGCAGGGTCCACTTTAA CCATTCGCCTTAGGATAGAGACGGGGACAGAACCCCCTGTGGCAGTG

In one embodiment, the nucleic acid sequence encoding the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, comprises or consists of a nucleic acid sequence presenting a sequence identity of at least 70%, preferably a sequence identity of at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more, with the nucleic acid sequence SEQ ID NO: 27, a variant and/or a fragment thereof.

In one embodiment, the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, is labeled with a detectable label.

The present invention thus relates to a PERV-B.RBD ligand as described herein, wherein said RBD ligand is coupled to a detectable label.

Examples of detectable labels include, but are not limited to, radioactive labels, paramagnetic metals, fluorescents labels and peptidic tags.

In one embodiment, the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, is labeled with a radioactive label. Examples of radioactive labels include, but are not limited to, non-metallic radioisotopes and radioactive metals.

Examples of non-metallic radioisotopes comprise, but are not limited to, 1-125, 1-123, 1-131 , C-l 1 , F-18, Br-75, Br-76, Br-77, Br-80, and At-2l 1. The non-metallic radioisotopes may be conjugated covalently to either terminus of the ligand, functional groups of amino acid side chains, be part of a linear stabilized peptide as an additional substituent, e.g., in an amino acid phenylalanine or tyrosine carrying fluorine, bromine or iodine, or as an additional substituent carboxy or methyl, or as a replacement of any regular carbon atom in the ligand. These radioisotopes are useful in ligands as positron emission tomography (PET) probes or as single-photon emission computed tomography (SPECT) probes. Examples of radioactive metals include, but are not limited to, Cu-64, Cu-67, Ga-67, Ga- 68, Zr-89, Y-90, Tc-99m, In - 111, Tb-l6l, Lu-I 77, Re-l86, Re- 188, and Bϊ-213. The radioactive metals may be covalently attached to the ligands, directly connected to the ligands or through a spacer.

In one embodiment, the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, is labeled with paramagnetic metals.

Examples of paramagnetic metals comprise, but are not limited to, Gd, Fe, Mn. The paramagnetic metals may be covalently attached to the ligands, directly connected to the ligands or through a spacer. These ligands are useful as magnetic resonance imaging (MRI) probes. In one embodiment, the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, is label ed with a fluorescent label. Exampl e of fluorescent label include, but are not limited to, fluorescent organic dyes, quantum dots and fluorescent protein. These ligands may be useful as optical imaging probes.

Example of fluorescent organic dyes include but are not limited to, commercial Alexa Fluor ^® dyes, fluorescein, rhodamine, or Cy ^® dyes (such as Cy3, Cy3.5, Cy5, Cy5.5, Cy7, and Cy7.5).

Example of fluorescent proteins include, but are not limited to, BFP, CFP, GFP, EGFP, mCherry, tdTomato, mPlum, mStrawberry, J-Red, DS-Red, mOrange, mCitrine, Venus, Ypet, YFP, Emerald, and the like. Another example of fluorescent protein is phycoerythrin. The fluorescent protein may be fused to the ligand by techniques of molecular cloning well known in the art.

In one embodiment, the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, is labeled with a peptidic tag. Example of peptidic tags include, but are not limited to, an antibody crystallizable region (Fc), Enzymes (alkaline phosphatase or horseradish peroxidase), Hemagglutinin tag, Poly Arginine tag, Poly Histidine tag, Myc tag, Strep tag, S-tag, HAT tag, 3x Flag tag, Calmodulin-Binding Peptide tag, SBP tag, Chitin Binding Domain tag, GST tag, Maltose- Binding Protein tag, Fluorescent Protein tag, T7 tag, V5 tag, X-press tag and the like. The peptidic tag may be fused to the ligands by techniques of mol ecular cloning well known in the art or covalently attached to the ligands.

In one embodiment, the PERV-B.RBD ligand, a variant and/or a fragment thereof, labeled as described herein is a fusion protein comprising a part or the totality of a RBD domain (as described herein), fused to a detection tag, such as, for example, a Fc fragment or a GFP. In one embodiment the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, is fused to a Fc fragment or a fluorescent protein. In one embodiment, the PERV-B.RBD ligand, a variant and/or a fragment thereof, labeled as described herein is a fusion protein comprising a part or the totality of a RBD domain (as described herein), fused to phycoerythrin.

Exampl es of Fc fragments include, but are not limited to, rabbit Fc fragment (amino acid sequence SEQ ID NO: 9, encoded by SEQ ID NO: 10), mouse Fc fragment (amino acid sequence SEQ ID NO: 11, encoded by SEQ ID NO: 12).

(SEQ ID NO: 9) APSTCSKPTCPPPELLGGPSVFIFPPKPKDTLMISRTPEVTCVVVDVSQDDPEVQF TWYINNEQVRTARPPLREQQFDCTIRVVSTLPIAHQDWLRGKEFKCKVHNKAL PAPIEKTISKARGQPLEPKVYTMGPPREELSSRSVSLTCMINGFYPSDISVEWEKN GKAEDNYKTTPAVLDSDGSYFLYSKLSVPTSEWQRGDVFTCSVMHEALHNHY TQKSISRSPGK (SEQ ID NO: 10)

GCACCCTCGACATGCAGCAAGCCCACGTGCCCACCCCCTGAACTCCTGGGG

GGACCGTCTGTCTTCATCTTCCCCCCAAAACCCAAGGACACCCTCATGATCT

CACGCACCCCCGAGGTCACATGCGTGGTGGTGGACGTGAGCCAGGATGACC CCGAGGTGCAGTTCACATGGTACATAAACAACGAGCAGGTGCGCACCGCCC

GGCCGCCGCTACGGGAGCAGCAGTTCAACAGCACGATCCGCGTGGTCAGCA CCCT CCCCATCACGCACC AGGACT GGCT GAGGGGC AAGGAGTTCAAGT GCA AAGTCCACAACAAGGCACTCCCGGCCCCCATCGAGAAAACCATCTCCAAAG CCAGAGGGCAGCCCCTGGAGCCGAAGGTCTACACCATGGGCCCTCCCCGGG AGG AGCT GAGC AGC AGGTCGGTC AGCCT GACCT GC AT GATC AACGGCTT CT ACCCTTCCGACATCTCGGTGGAGTGGGAGAAGAACGGGAAGGCAGAGGAC AACTACAAGACCACGCCGGCCGTGCTGGACAGCGACGGCTCCTACTTCCTC T AC AAC AAGCT CT C AGT GCCC ACG AGT G AGT GGC AGC GGGGCG AC GT CTTC ACCTGCTCCGTGATGCACGAGGCCTTGCACAACCACTACACGCAGAAGTCC ATCTCCCGCTCTCCGGGTAAATGA

(SEQ ID NO: 11)

VDVPRDCGCKPCICTVPEVSSVFIFPPKPKDVLTITLTPKVTCVYVDISKDDPEYQ FSWFVDDVEVHTAQTQPREEQFNSTFRSVSELPIMHQDWLNGKEFKCRVNSAA FPAPIEKTISKTKGRPKAPQVYTIPPPKEQMAKDKVSFTCMITDFFPEDITVEWQ WN GQP AENYK T QPIMDTDGS YF VY SKENV QKSNWE AGNTFTCS VEHEGEHN HHTEKSLSHSPGK

(SEQ ID NO: 12)

GT CGACGTGCCCAGGGATT GT GGTT GTAAGCCTT GCATATGTACAGTCCC AG AAGTATCATCTGTCTTCATCTTCCCCCCAAAGCCCAAGGATGTGCTCACCAT T ACT CT G ACTCCT AAGGT C ACGT GT GTT GT GGT AG AC AT C AGC AAGG AT GAT C CCG AGGT C C AGTT C AGCT GGTTT GT AG AT GAT GT GG AGGT GC AC AC AGCT CAGACGCAACCCCGGGAGGAGCAGTTCAACAGCACTTTCCGCTCAGTCAGT GAACTTCCC AT CAT GC ACC AGGACT GGCT C AAT GGC AAGG AGTT C AAAT GC AGGGTCAACAGTGCAGCTTTCCCTGCCCCCATCGAGAAAACCATCTCCAAA ACCAAAGGCAGACCGAAGGCTCCACAGGTGTACACCATTCCACCTCCCAAG GAGC AGAT GGCC AAGG ATAAAGTC AGTCTGACCT GC AT GATAAC AGACTTC TTC CCT G AAG AC ATT ACT GTGG AGTGGC AGT GGAAT GGGC AGC C AGCGG AG AACT AC AAG AAC ACT C AGCCC AT CAT GG AC AC AG AT GGCT CTT ACTTCGT CT ACAGCAAGCTCAATGTGCAGAAGAGCAACTGGGAGGCAGGAAATACTTTCA

CCTGCTCTGTGTTACATGAGGGCCTGCACAACCACCATACTGAGAAGAGCC

TCTCCCACTCTCCTGGTAAATGA

In one embodiment, the PERV-B.RBD ligand of the invention, is fused to a Fc fragment, and comprises or consists of the amino acid sequence SEQ ID NO: 13, a variant and/or a fragment thereof.

(SEQ ID NO: 13)

MHPTLSWRHLPTRGGEPKRLRIPLSFASIAWFLTLTITPQASSKRLIDSSNPHRPL SLTWLIIDPDT G VTYNSTRGVAPRGT WWPELHF CLRLINP AVKSTPPNL VRS Y G FYCCPGTEKEKYCGGSEESFCRRWSCVTSNDGDWKWPISLQDRVKFSFVNSGP GKYKVMKL YKDKS C SP SDLD YLKI SFTEKGKQENIQKWIN GMS WGI VF YKY G GGAGSTLTIRLRIEAGTEPPYAVGSVDVPRDCGCKPCICTVPEVSSYFIFPPKPKD VLTITLTPKVT C VVVDISKDDPE V QFS WF VDD VE VHT AQT QPREEQFNSTFRS V SELPIMHQDWLNGKEFKCRVNSAAFPAPIEKTISKTKGRPKAPQVYTIPPPKEQM AKDKVSLTCMITDFFPEDITVEWQWNGQPAENYKNTQPIMDTDGSYFVYSKLN VQKSNWEAGNTFTCSVLHEGLHNHHTEKSLSHSPGK

In one embodiment, the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, is fused to a Fc fragment and does not comprise a signal peptide. In one embodiment, the PERV-B.RBD ligand fused to a Fc fragment comprises or consists of amino acids 44 to 469 of SEQ ID NO: 13, or a variant thereof.

In one embodiment, the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, is fused to a Fc fragment and does not comprise a signal peptide. In one embodiment, the PERV-B.RBD ligand fused to a Fc fragment comprises or consists of amino acids 39, 40, 41, 42, 43, 44, 45, 46, 47, 48 or 49 to 469 of SEQ ID NO: 13, or a variant thereof.

In one embodiment, the amino-acid sequence of the PERV-B.RBD ligand of the invention is fused to a Fc fragment and, compri ses or consists of an amino acid sequence presenting a sequence identity of at least about 70%, preferably a sequence identity of at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more, with the amino acid sequence SEQ ID NO: 13, a variant and/or a fragment thereof.

In one embodiment, PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof is fused to a Fc fragment, and is encoded by a nucleic acid sequence comprising or consisting of the nucleic acid sequence SEQ ID NO: 14, a variant and/or a fragment thereof.

(SEQ ID NO: 14)

AT GC ATCCC ACGTTAAGCTGGCGCC ACCT CCCGACT CGGGGT GGAGAGCCG AAAAGACTGAGAATCCCCTTAAGCTTCGCCTCCATCGCCTGGTTCCTTACTC TAACAATAACTCCCCAGGCCAGTAGTAAACGCCTTATAGACAGCTCGAACC CCCATAGACCTTTATCCCTTACCTGGCTGATTATTGACCCTGATACGGGTGT C ACT GT AAAT AGC ACT C G AGGT GTT GCTCCT AG AGGC ACCT GGT GGCCT G A ACTGCATTTCTGCCTCCGATTGATTAACCCCGCTGTTAAAAGCACACCTCCC AACCT AGT C CGT AGTT AT GGGTT CT ATT GCT GCC C AGGC AC AG AG AAAG AG AAATACTGT GGGGGTTCT GAGGAATCCTTCT GT AGGAGAT GGAGCT GCGTC ACCTCCAACGATGGAGACTGGAAATGGCCGATCTCTCTCCAGGACCGGGTA AAATT CT CCTTT GT C AATTCCGGCCCGGGC AAGTAC AAAGT GATGAAACTAT AT AAAG AT AAG AGCT GCTCC CC AT C AG ACTT AG ATT AT CT AAAG AT AAGTTT C ACT G AAAAAGG AAAAC AGG AAAAT ATT C AAAAGT GG AT AAAT GGT AT G A GCTGGGGAATAGTTTTTTATAAATATGGCGGGGGAGCAGGGTCCACTTTAA CCATTCGCCTTAGGATAGAGGCGGGGACAGAACCCCCTGTGGCAGTGGGAT CCGTCGACGTGCCCAGGGATTGTGGTTGTAAGCCTTGCATATGTACAGTCCC AGAAGTATCATCTGTCTTCATCTTCCCCCCAAAGCCCAAGGATGTGCTCACC ATTACTCTGACTCCTAAGGTCACGTGTGTTGTGGTAGACATCAGCAAGGATG ATCC CG AGGTCC AGTT C AGCT GGTTT GT AG AT GAT GT GG AGGT GC AC AC AG CTCAGACGCAACCCCGGGAGGAGCAGTTCAACAGCACTTTCCGCTCAGTCA GT GAACTTCCC ATC AT GC ACC AGGACT GGCTC AAT GGC AAGGAGTT C AAAT GCAGGGTCAACAGTGCAGCTTTCCCTGCCCCCATCGAGAAAACCATCTCCA AAACCAAAGGCAGACCGAAGGCTCCACAGGTGTACACCATTCCACCTCCCA AGGAGC AGAT GGCCAAGGAT AAAGT C AGT CT GACCT GC AT GAT AAC AGACT TCTTCCCT G AAG AC ATT ACT GT GG AGT GGC AGT GG AAT GGGC AGCC AGCGG

AG AACT AC AAG AAC ACT C AGCC C AT CAT GG AC AC AG ATGGCTCTT ACTT C G

TCTACAGCAAGCTCAATGTGCAGAAGAGCAACTGGGAGGCAGGAAATACTT

TCACCTGCTCTGTGTTACATGAGGGCCTGCACAACCACCATACTGAGAAGA

GCCTCTCCCACTCTCCTGGTAAATGATCCCAGTGTCCTTGGAGCCCTCTGGT

CCTACAgcggccgcTCTAG

In one embodiment, the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, is fused to a Fc fragment and is encoded by a nucleic acid sequence comprising or consisting of a nucleic acid sequence presenting a sequence identity of at least about 70%, preferably a sequence identity of at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more, with the nucleic acid sequence SEQ ID NO: 14, a variant and/or a fragment thereof.

In one embodiment, the PERV-B.RBD ligand of the invention, a fragment and/or a variant thereof, is coupled with at least one detectable label. Non-limiting examples of contrast agents are listed herein. In one embodiment, the contrast agent is 1-125.

In one embodiment, the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, coupled with at least one detectable label may be used as a probe for medical imaging.

The term medical imaging as used herein refers to imaging techniques suitable to visualize in vivo a subject’s internal structures ( i.e . tissues or organs). Such techniques include but are not limited to, computed tomography (CT scan), endoscopic ultrasound (EUS), magnetic resonance imaging (MRI), positron-emission tomography (PET), single photon emission tomography (SPECT), magnetic resonance cholangiopancreatography, fluorimetry, fluorescence, and near-infrared (NIR) fluorescent imaging. In the context of the invention the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, coupled with at least one detectable label may be used as a probe, to localize in vivo SM VT-expressing cells in a subject’s internal structures.

In one embodiment of the invention, the at least one PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, coupled with at least one detectable label is for use as a tracer. The present invention thus further relates to the use as a tracer of a PERV-B.RBD ligand, a variant and/or a fragment thereof, coupled with at least one detectable label. The term“tracer”, as used herein, refers to a recognition agent providing insight into SMVT-related disease location, progression and/or structure for pre-, intra- and post-operative surgery.

In one embodiment, the PERV-B.RBD ligand of the invention is a variant of one of the polypeptides having an amino acid sequence selected from the group comprising or consisting of SEQ ID NO: 2, 4, 5, 6, 13, 17, 18, 19, 20, 21 and 22, and fragments thereof, preferably a variant of one of the polypeptides having an amino acid sequence selected from the group comprising or consisting of SEQ ID NO: 5, 6, 13, 19, 20, 21 and 22, and fragments thereof.

In one embodiment, the PERV-B.RBD ligand of the invention is a variant of one of the polypeptides having an amino acid sequence selected from the group comprising or consisting of SEQ ID NO: 2, 4, 5, 6, 13, 17, 18, 19, 20, 21, 22, 25 and 26, and fragments thereof, preferably a variant of one of the polypeptides having an amino acid sequence selected from the group comprising or consisting of SEQ ID NO: 5, 6, 13, 19, 20, 21 and 22, and fragments thereof.

In one embodiment, a variant of a sequence selected from SEQ ID NO: 2, 4, 5, 6, 13, 17, 18, 19, 20, 21 and 22 and fragments thereof is capable of binding to SMVT with an affinity at least equivalent to the one of SEQ ID NO: 2, 4, 5, 6, 13, 17, 18, 19, 20, 21 and 22 or a fragment thereof, respectively.

In one embodiment, a variant of a sequence selected from SEQ ID NO: 2, 4, 5, 6, 13, 17, 18, 19, 20, 21, 22, 25 and 26 and fragments thereof is capable of binding to SMVT with an affinity at least equivalent to the one of SEQ ID NO: 2, 4, 5, 6, 13, 17, 18, 19, 20, 21, 22, 25 and 26 or a fragment thereof, respectively.

In one embodiment, a variant of a sequence selected from SEQ ID NO: 2, 4, 5, 6, 13, 17, 18, 19, 20, 21 and 22 and fragments thereof comprises conservative amino acid substitutions as compared to the sequence SEQ ID NO: 2, 4, 5, 6, 13, 17, 18, 19, 20, 21 or 22 or a fragment thereof, respectively, such as, for example, 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 conservative amino acid substitutions.

In one embodiment, a variant of a sequence selected from SEQ ID NO: 2, 4, 5, 6, 13, 17, 18, 19, 20, 21, 22, 25 and 26 and fragments thereof comprises conservative amino acid substitutions as compared to the sequence SEQ ID NO: 2, 4, 5, 6, 13, 17, 18, 19, 20, 21,

22, 25 or 26 or a fragment thereof, respectively, such as, for example, 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 conservative amino acid substitutions.

In another embodiment, a variant of a sequence selected from SEQ ID NO: 2, 4, 5, 6, 13, 17, 18, 19, 20, 21 and 22 and fragments thereof is a polypeptide wherein 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 amino acids from the sequence SEQ ID NO: 2, 4, 5, 6, 13, 17, 18, 19, 20, 21 or 22 or a fragment thereof respectively, is/are absent, or substituted by any amino acid, or wherein 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 amino acids (either contiguous or not) is/are added.

In another embodiment, a variant of a sequence selected from SEQ ID NO: 2, 4, 5, 6, 13, 17, 18, 19, 20, 21, 22, 25 and 26 and fragments thereof is a polypeptide wherein 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 amino acids from the sequence SEQ ID NO: 2, 4, 5, 6, 13, 17, 18, 19,

20, 21 , 22, 25 or 26 or a fragment thereof respectively, is/are absent, or substituted by any amino acid, or wherein 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 amino acids (either contiguous or not) is/are added.

The PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, may be modified by means well-known in the art, for instance by the addition of one or more functional group such as a phosphate, acetate, lipid or carbohydrate group, and/or by the addition of one or more protecting group. For example, the RBD ligands can be modified by the addition of one or more functional groups such as phosphate, acetate, or various lipids and carbohydrates. The RBD ligands of the invention can also exist as polypeptide derivatives. The term“polypeptide derivative” refers to compound having an amino group (— NH— ), and more particularly, a peptide bond. Polypeptides may be regarded as substituted amides. Like the amide group, the peptide bond shows a high degree of resonance stabilization. The C— N single bond in the peptide linkage has typically about 40 percent double-bond character and the C=0 double bond about 40 percent single -bond character.“Protecting groups” are those groups that prevent undesirable reactions (such as proteolysis) involving unprotected functional groups. Specific examples of amino protecting groups include formyl; trifluoroacetyl; benzyloxycarbonyl; substituted benzyloxycarbonyl such as (ortho- or para-) chlorobenzyloxycarbonyl and (ortho- or para-) bromobenzyloxycarbonyl; and aliphatic oxycarbonyl such as t-butoxycarbonyl and t-amiloxycarbonyl. The carboxyl groups of amino acids can be protected through conversion into ester groups. The ester groups include benzyl esters, substituted benzyl esters such as methoxybenzyl ester; alkyl esters such as cyclohexyl ester, cycloheptyl ester or t-butyl ester. The guanidino moiety may be protected by nitro; or arylsulfonyl such as tosyl, methoxybenzensulfonyl or mesitylenesulfonyl, even though it does not need a protecting group. The protecting groups of imidazole include tosyl, benzyl and dinitrophenyl. The indole group of tryptophan may be protected by formyl or may not be protected.

The modification of the RBD ligands may aim at improving their lifetime in vivo. One type of modification is the addition to the N- or C -term ini of the RBD ligands of polyethylene glycol (PEG). PEG is known by the person skilled in the art to have many properties that make it an ideal carrier for polypeptides such as high water-solubility, high mobility in solution and low immunogenicity. This modification also protects the polypeptides from exopeptidases and therefore increases their overall stability in vivo. Other modifications used to prevent degradation of the polypeptides by endopeptidases or exopeptidases include N-terminal modifications such as acetylation or glycosylation, C -terminal modifications such as amidation and use of unnatural amino acids (b -amino and a-trifluoromethyl amino acids) at particular sites within the polypeptides. Another alternative to increase polypeptide molecular size is the genetic fusion of the polypeptides to the Fc domain of human immunoglobulin (including, for example, IgA, IgM and IgG) or the fusion of the polypeptides to albumin.

In one embodiment, the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, is glycosylated. In another embodiment, the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof is not glycosylated. The RBD ligands of the invention described herein can be produced synthetically by chemical synthesis or enzymatic synthesis as it is well known in the art. Alternatively, nuc leotide sequences encoding the polypeptides of the invention can be introduced into a protein expression vector and produced in a suitable host organism ( e.g ., bacteria, insect cells, etc.), then purified. In one embodiment, the receptor-binding domain ligand is obtained by a cloning method, such as, for example, using any production system known in the art, such as, for example, a bacterial cell (such as, for example, E. coli), yeast, baculovirus-insect cell, or mammalian cells such as HEK or CHO, expression system.

Methods for coupling at least one detectable label to an RBD ligand are well known in the state of the art. For instance, the at least one detectable label may be bound covalently or non-covalently.

Techniques to couple polypeptides to 1-125 are well known in the state of the art. A non- limited example of such a method is the following: iodine present in a reduced form (Nal) reacts with the phenol group of a tyrosine or with the side chain of a histidine residue. These groups are pre-oxidized with an oxidizing agent (iodogen). The peptides preparation (100 pg for lmci = 37 MBq) is then added to an iodogen solution and incubated for 10 minutes at 4°C. The reaction is stopped using a stop solution comprising for example 200 pL of PBS with sodium azide per marking. In parallel, a mouse serum is added onto a PD 10 column. Then the reaction solution is added onto the PD 10 column and the peptide coupled with the iodine is collected.

In embodiments concerning detectable labels encoded by a nucleic acid sequence, the detectable label may be fused to the RBD ligand of the invention, a variant and/or a fragment thereof, by techniques of molecular cloning well known in the art.

In one embodiment, the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, binds to SMVT.

In one embodiment, the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, binds specifically to SMVT. The expression "specifically binds to", as used herein, refers to the binding specificity and affinity of a molecule or a domain thereof for a particular target or epitope, or a domain thereof, even in the presence of a heterogeneous population of other proteins and biological molecules. Thus, in one embodiment, under designated assay conditions, the ligand described in the invention binds preferentially to its target and does not bind in a significant amount to other components present in a test sample or subject. In one embodiment, such a ligand shows high affinity binding to its target with an equilibrium dissociation constant equal or below 1 x l0 ⁶ M ( e.g ., at least 0.5 x l0 ⁶ , 1 x l0 ⁷ , 1 x l0 ⁸ , 1 x l0 ⁹ , 1 x l0 ¹⁰ and less). Standard assays to evaluate the binding ability of two biological molecules are known in the art, including for example, ELISAs, Western blots,

RIAs and flow cytometry. The binding kinetics (e.g., binding affinity) of the molecules also can be assessed by standard assays known in the art, such as by Biacore analysis.

The methods of the invention comprise the step of detecting and/or measuring the binding of a PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, to SMVT in a biological sample.

Techniques to measure the binding of a ligand to its receptor are known in the art and may imply the detection and measure of the amount of the ligand-receptor complexes. In the context of the present invention, such techniques could for example rely on the detection and measure of the amount of complexes formed by PERV-B.RBD ligands, variants and/or fragments thereof with SMVT present in the biological sample, such as, for example, at the cell surface of cells present in the biological sample

Example of such technique include, but are not limited to, flow cytometry analysis, immunohistochemistry, western blot associated or not with cell fractionation, enzyme- linked immunosorbent assay (ELISA), sandwich ELISA, fluorescent-linked immunosorbent assay (FLISA), enzyme immunoassay (El A), radioimmunoassay (RIA), image analysis, for example high content analysis, computed tomography (CT scan), endoscopic ultrasound (EUS), magnetic resonance imaging (MRI), positron-emission tomography (PET), single photon emission tomography (SPECT), magnetic resonance cholangiopancreatography, fluorimetry, fluorescence, and near-infrared (NIR) fluorescent imaging and the like. Examples of such techniques amenable to an in vitro use include, but are not limited to, immunohistochemistry, Multiplex methods (Luminex), western blot, enzyme-linked immunosorbent assay (ELISA), sandwich ELISA, fluorescent-linked immunosorbent assay (FLISA), enzyme immunoassay (EIA), radioimmunoassay (RIA), flow cytometry (FACS), and the like.

Examples of such techniques suitable for an in vivo use include, but are not limited to, computed tomography (CT scan), endoscopic ultrasound (EUS), magnetic resonance imaging (MRI), positron-emission tomography (PET), single photon emission tomography (SPECT), magnetic resonance cholangiopancreatography, fluorimetry, fluorescence, and near-infrared (NIR) fluorescent imaging.

In one embodiment, the methods of the invention further comprise a step of comparing the binding of the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, to SMVT measured at step b. with a reference value.

As used herein, the term“reference” broadly encompasses any suitable reference binding level which may be used as a basis for comparison with respect to the determined binding.

In one embodiment, the reference is constructed using algorithms and/or other methods of statistical and hierarchical classification. In another aspect, the reference binding level is stored in a database to provide a stored binding level and the stored binding level is used to determine the difference in the binding level. The database may, for example, be stored on a computer or a server.

In one embodiment, the reference binding level is an index value or is derived from one or more risk prediction algorithms or computed indices for the presence of cells wherein the function and/or expression of SMVT is altered ( e.g ., increased or decreased). A reference binding level can be relative to a number or value derived from population studies, including without limitation, such populations of subjects having similar age range, subjects in the same or similar ethnic group.

In one embodiment, the reference value is determined by measuring the binding of the PERV-B.RBD ligand of the invention, a fragment and/or a variant thereof, to SMVT in a reference population. In one embodiment, the reference population refers to a population comprising at least 1 , preferably at least 5, at least 10, at least 15, at least 20, at least 25, at least 30, at least 35, at least 40, at least 45, at least 50, at least 75, at least 100 or more substantially healthy subjects, i.e., subject who are not affected and/or who have not been diagnosed with the SMVT-related disease being considered. According to this embodiment, a determined binding level different from the reference binding level may be indicative of the presence of a SMVT related disease.

In another embodiment, the reference population refers to a population comprising at least 1, preferably at least 5, at least 10, at least 15, at least 20, at least 25, at least 30, at least 35, at least 40, at least 45, at least 50, at least 75, at least 100 or more subjects affected

(and preferably diagnosed) with the SMVT-related disease being considered. According to this embodiment, a determined binding level different from the reference binding level may be indicati ve of the absence of a SMVT related disease.

In the present invention, two numeric values, in particular two binding levels, are considered as di fferent if the first numeric value is higher (such as, for example, the first numeric value is about 20% higher than the second one, preferably is about 30, 40, 50, 60, 70, 80, 90% or more higher than the second one) or lower than the second one (such as, for example, the second numeric value is about 20% lower than the second one, preferably is about 30, 40, 50, 60, 70, 80, 90% or more lower than the second one). In one embodiment, two numeric values, in particular two binding levels, are considered as different if the first numeric value is increased by a factor of or above about 1.01, preferably by a factor of or above, about 1.02, 1.03, 1.04, 1.05, 1.06, 1.07, 1.08, 1.09, more preferably the value is increased by a factor of or above about 1.1, 1.15, 1.20, 1.25, 1.30, 1.3, 1.35, 1.40, 1.45, 1.50, 1.55, 1.60, 1.65, 1.70, 1.75, 1.80, 1.85, 1.90, 1.95, more preferably by a factor of or above about 2, 3, 4, .5 or more when compared to the second value or if the first numeric value is decreased by a factor of or below about 0.99, preferably by a factor of or below, about 0.98, 0.97, 0.96, 0.95, 0.94, 0.93, 0.92, 0.91, more preferably the value is decreased by a factor of or below about 0.90, 0.85, 0.80, 0.75, 0.70, 0.65, 0.60, 0.55, 0.50, 0.45, 0.40, 0.35, 0.30, 0.25, 0.20, 0.15, 0.1 or less when compared to the second value. In one embodiment, by implying a multitude of measures of the binding of the PERV- B.RBD ligand of the invention to SMVT in the reference population, it is conceivable to use as reference value a mathematical representation of the binding of the PERV-B.RBD ligand of the invention to SMVT such as for example, a mean or a median. In one embodiment, the reference value is a personalized reference, determined at different time points in the same subject (such as, for example, before receiving a treatment for a SMVT -related disease).

In one embodiment, the reference value is an internal reference value, determined in different part of the same subject, such as, for example, in different organs or tissues. This type of reference value is in particular useful in the implementation of method based on medical imaging.

In one embodiment, the in vitro method of the present invention is for diagnosing a SMVT -related disease in a subject, or for identifying a subject as presenting a risk of developing an SMVT -related disease. The present invention thus also relates to in vitro methods for diagnosing a SMVT -related disease in a subject, or for identifying a subject as presenting a risk of developing an SMVT -related disease, wherein said methods comprises the steps of:

a. contacting a biological sample from the subject with at least one PERV- B.RBD ligand, a variant and/or a fragment thereof; and, b. measuring the binding of said PERV-B.RBD ligand, variant and/or fragment thereof to SMVT.

The present invention relates to an in vitro method for diagnosing a subject with or identifying a subject as being at risk of developing a SMVT -related disease comprising the steps of:

a. contacting a biological sample previously obtained from said subject with a PERV-B.RBD ligand, a variant and/or a fragment thereof;

b. measuring the binding of said PERV-B.RBD ligand, variant and/or fragment thereof to SMVT; and,

c. comparing the binding measured at step b. with a reference value. In one embodiment, the step of comparing the binding of the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, to a reference value allows to diagnose a subject with, or at risk of developing, a SMVT -related disease.

In one embodiment, the SMYT-related disease is cancer, a disorder of pregnancy, an infectious disease or a neurodegenerative disease.

In one embodiment, the SMVT -related disease is cancer, a disorder of pregnancy, an infectious disease or a neuroinflammatory disease.

In one embodiment, the SMVT -related disease is a disorder related to a mutation within the SLC5A6 gene. In one embodiment, the SMVT -related disease is cancer, preferably cancer selected from the group comprising or consisting of liver cancer, prostate cancer, lung cancer, gallbladder cancer, pancreas cancer, colon cancer, ovarian cancer, brain cancer, kidney cancer, thyroid cancer, lymphomas, urothelial cancer, cervical cancer and endometrial cancer. In one embodiment, the SMVT -related disease is cancer, preferably cancer selected from the group comprising or consisting of liver cancer, prostate cancer, lung cancer, gallbladder cancer, pancreas cancer, colon cancer, ovarian cancer, brain cancer, kidney cancer, thyroid cancer, and lymphomas.

Examples of liver cancers include, but are not limited to, hepatoma, hepatocellular carcinoma, cholangiocarcinoma, hepatoblastoma, angiosarcoma, hepatocellular adenoma, and hemangioma.

In one embodiment, said liver cancer is a hepatocellular carcinoma or a cholangiocarcinoma.

In one embodiment, said liver cancer is a hepatocellular carcinoma. Examples of prostate cancers include, but are not limited to, adenocarcinoma, and sarcoma. Examples of lung cancers include, but are not limited to non-small cell lung carcinoma, adenocaminoma, bronchogenic carcinoma, alveolar carcinoma, bronchiolar carcinoma, bronchial adenoma, lung sarcoma, lymphoma, chondromatous hamartoma, and pleural mesothelioma. In one embodiment, said lung cancer is a non-small cell lung carcinoma.

Examples of pancreas cancers include, but are not limited to, ductal adenocarcinoma, insulinoma, glucagonoma, gastrinoma, carcinoid tumors, and vipoma.

Examples of colon cancers include, but are not limited to large bowel or large intestines cancer (such as, e.g., adenocarcinoma, tubular adenoma, villous adenoma, hamartoma or leiomyoma), and colorectal cancer.

Examples of ovarian cancers include, but are not limited to, dysgerminoma, granulosa- theca cell tumors, and Sertoli-Leydig cell tumors.

Examples of brain cancers include, but are not limited to, astrocytoma, medulloblastoma, glioma, lower grade glioma, ependymoma, germinoma (pinealoma), glioblastoma multiform, oligodendroglioma, schwannoma, retinoblastoma, congenital tumors, spinal cord neurofibroma, glioma, and sarcoma.

Example of kidney cancer include, but are not limited to, clear renal cell carcinoma, chromophobe renal cell carcinoma, papillary renal cell carcinoma, adenocarcinoma, Wilm’s tumor, and nephroblastoma. Other examples of cancer include, but are not limited to, lymphoma and leukemia.

Example of thyroid cancers include, but are not limited to, anaplastic thyroid carcinomas.

Examples of lymphomas include, but are not limited to, Hodgkin lymphoma, and non- Hogdkin lymphomas.

In one embodiment, the SMYT-related disease is prostate cancer. In one embodiment, the SMVT-related disease is a neurodegenerative disease, such as, for example, multiple sclerosis or Huntington’s disease.

In one embodiment, the SMVT-related disease is a neuroinflammatory disease, preferably multiple sclerosis. In one embodiment, the SMVT-related disease is a disorder of pregnancy, preferably pre eclampsia, or intrauterine growth retardation.

In one embodiment, the SMVT-related disease is a disorder associated with anomalies of placental and/or fetal development, such as, for example, intrauterine growth retardation.

In one embodiment, the SMVT-related disease is a disorder related to a mutation within the SLC5A6 gene. In one embodiment, said mutation within the SLC5A6 results in a partial or complete loss of function or partial or complete loss of expression.

In one embodiment, the SMVT-related disease is a disorder related to a mutation within the SLC5A6 gene, such as, for example the mutation described by Subramanian et al (Hum Genet. 2017, February; 136(2): 253-261), which is associated with failure to thrive, microcephaly and brain changes on MR1, cerebral palsy and developmental delay, variable immunodeficiency, severe gastro-esophageal reflux requiring a gastrostomy tube/ fundoplication, osteoporosis and pathologic bone fractures. Another example of a mutation within the SLC5A6 gene is the mutation described by Schwantje et al. (HMD Rep. 2019 May 28;48(l):l 1-14), leading to biotin deficiency, symptoms and metabolites levels similar to those observed in cases of biotinidase deficiency.

In one embodiment, the SMVT-related disease is an infectious disease,

As defined hereinabove,“infectious disease” as used herein encompasses any disease caused by an infectious agent such as a virus, a bacterium, a fungus, a protozoan parasite or a prion protein. In one embodiment, said infectious disease is caused by a virus. In other words, in one embodiment, said infectious disease is a viral infection. Examples of viruses that may be responsible for a viral infection include, without being limited to, viruses of the families Arenaviridae, Astroviridae, Bimaviridae, Bromoviridae, Bunyaviridae, Calicivmdae, Closteroviridae, Comoviridae, Cystoviridae, Flaviviridae, Flexiviridae, Hepadnaviridae, Hepevirus, Herpesviridae, Leviviridae, Luteoviridae, Mononegavirales, Mosaic Viruses, Nidovirales, Nodaviridae, Orthomyxoviridae, Paramyxoviridae, Papillomavmdae, Picobirnavirus, Picomaviridae, Potyviridae, Reoviridae, Retroviridae, Sequiviridae, Tenuivirus, Togaviridae,

Tombusviridae, Totivmdae, and Tymoviridae.

In one embodiment, said infectious disease is caused by a bacterium, preferably belonging to the order Enterobacteriales .

In one embodiment, said infectious disease is caused by a bacterium, preferably belonging to the genus Salmonella. In other words, in one embodiment, said infectious disease is a Salmonella infection.

Examples of bacteria that may be responsible for a bacterial infection include, without being limited to, bacteria of the genera Bacillus, including Bacillus anthracis and Lactobacillus, Brucella, Bordetella including B. pertussis and B. bronchiseptica; Camplyobacter; Chlamydia including C. psittaci and C. trachomatis, Samonella including S. bongori and S. enterica Cotynebacterium including C. diphtheriae; Enterobacter including E. aerogenes; Enterococcus, Escherichia including E. coir, Flavobacterium including F. meningosepticum and F. odoratum; Gardnerella including G. vaginalis, Klebsiella, Legionella including L. pneumophila, Listeria, Mycobacterium including M. tuberculosis, M. intrace llulare, M . folluiturn, M. laprae, M. avium, M. bovis, M. africanum, M. kansasii, and M. lepraemurium; Neisseria including N. gonorrhoeae and N. meningitides; Nocardia; Proteus including P. mirabilis and P. vulgaris, Pseudomonas including P. aeruginosa, Rickettsia including R. rickettsii; Serratia including S. marcescens and S. Uquefaciens; Staphylococcus, Streptomyces including S. somaliensis, Streptococcus, including S. pyogenes, and Treponema.

In one embodiment, said infectious disease is caused by a fungus. In other words, in one embodiment, said infectious disease is a fungal infection. Examples of fungi that may be responsible for a fungal infection include, without being limited to, fungi of the genera Aspergillus, Candida, Cryptococcus, Epidermophyton, Microsporum, and Trichophyton.

In one embodiment, said infectious disease is caused by a protozoan parasite. In other words, in one embodiment, said infectious disease is a protozoan infection.

Examples of protozoan parasites that may be responsible for a protozoan infection include, without being limited to, Coccidia, Leishmania, Plasmodium, Toxoplasma and Trypanosoma.

In one embodiment, the method of the invention is for diagnosing or for assessing a risk of developing a SMVT -related disease associated with an increased SMVT level in a subject, and a binding of the PERV-B.RBD ligand, variant and/or fragment thereof to SMVT measured at step b. higher than the binding of the PERV-B.RBD ligand of the invention, variant and/or fragment thereof to SMVT measured in a reference population of substantially healthy subjects (or in a reference sample from a reference population) is indicative of the presence of said disease, or of a risk of developing said disease.

In one embodiment, the method of the invention is for diagnosing or for assessing a risk of developing a SMVT -related disease associated with an increased SMVT level at the cell surface in a subject, and a binding of the PERV-B.RBD ligand, variant and/or fragment thereof to SMVT measured at step b. higher than the binding of the PERV- B.RBD ligand of the invention, variant and/or fragment thereof to SMVT measured in a reference population of substantially healthy subjects (or in a reference sample from a reference population) is indicative of the presence of said disease, or of a risk of developing said disease.

Examples of SMVT -related diseases associated with an increased SMVT expression level and/or level of SMVT at the cell surface include, but are not limited to, lung cancer, liver cancer, prostate cancer, kidney cancer, thyroid cancer, pancreas cancer, colon cancer (in particular colorectal cancer), gallbladder cancer, urothelial cancer, cervical cancer and endometrial cancer. In one embodiment, the method of the invention is for diagnosing or for assessing a risk of developing a SMYT-related disease associated with a decreased SMVT level in a subject, and a binding of the PERV-B.RBD ligand, variant and/or fragment to SMVT measured at step b. lower than the binding of the PERV-B.RBD ligand, variant and/or fragment to SMVT measured in a reference population of substantially healthy subjects (or in a reference sampl e from a reference population) is indicative of the presence or of a risk of developing said disease.

In one embodiment, the method of the invention is for diagnosing or for assessing a risk of developing a SMVT -related disease associated with a decreased SMVT level at the cell surface in a subject, and a binding of the PERV-B.RBD ligand, variant and/or fragment to SMVT measured at step b. lower than the binding of the PERV-B.RBD ligand, variant and/or fragment to SMVT measured in a reference population of substantially healthy subjects (or in a reference sample from a reference population) is indicative of the presence or of a risk of developing said disease. Examples of SMVT -related diseases associated with a decreased SMVT expression level and/or SMVT level at the cell surface include, but are not limited to, lymphomas, ovarian cancer, and disorders of pregnancy.

The present invention also relates to in vivo methods for detecting and/or measuring the level of SMVT using a PERV-B.RBD ligand of the invention, a variant and/or fragment thereof.

In one embodiment, said in vivo method is for diagnosing a subject with or identifying a subject as being at risk of developing a SMVT -related disease.

The present invention thus relates to a PERV-B.RBD ligand as described herein, a variant and/or fragment thereof, for use in a in vivo diagnosis method of an SMVT -related disease in a subject. In one embodiment, said method comprises the detection and/or measure of the level of SMVT within the body of said subject, such as, for example, in a specific organ or tissue. The present invention also relates to a PERV-B.RBD ligand of the invention, a variant and/or fragment thereof, for use in a in vivo diagnosis method of cancer in a subject, wherein said method comprise the detection and/or measure of the level of SMVT in the body of said subject, such as, for example, in a specific organ. The present application also relates to a method for the in vivo diagnosis of a SMVT- related disease, comprising:

a. contacting at least one PERV-B.RBD ligand, a variant and/or a fragment thereof with a cell, a sample, a tissue or an organ, and

b. detecting and/or quantifying the at least one PERV-B.RBD ligand bound to SMVT present in the cell, sample, tissue or organ within said subject.

The present application also relates to a method for the in vivo diagnosis of SMVT -related disease comprising:

a. administering to a subject in need thereof at least one PERV-B.RBD ligand, a variant and/or a fragment thereof, and

b. detecting and/or quantifying the binding of at least one PERV-B.RBD ligand, variant and/or fragment thereof within said subject, for example by medical imaging.

In one embodiment, of the invention, the PERV-B.RBD ligand is coupled with at least one detectable label, and may be used for in vivo diagnosis by medical imaging. In one embodiment, the PERV-B.RBD ligand administered to the subject is comprised in a diagnostic composition.

The present invention also relates to a PERV-B.RBD ligand of the invention, a variant and/or fragment thereof, for use in a in vivo diagnosis method of an SMVT -related disease in a subject, wherein said method comprise the detection and/or measure of the level of SMVT using medical imaging techniques.

Examples of specific medical imaging techniques that may be used are well known to the skilled artisan and include, but are not limited to, computer assisted tomography (CAT), magnetic resonance spectroscopy (MRS), magnetic resonance imaging (MRI), positron emission tomography (PET) or single-photon emission computed tomography (SPECT) and are described in Boonstra et al. (2015. Oncotarget. 6(16): 14260-73).

The present invention thus relates to an in vivo method for diagnosing a subject with or identifying a subject at risk of developing an SMVT-related disease comprising the steps:

a. administering to said subject a labeled PERV-B.RBD ligand, a variant and/or a fragment thereof; and,

b. detecting and/or measuring the binding of said labeled PERV-B.RBD ligand, variant and/or fragment thereof to SMVT using medical imaging; c. optionally comparing a binding measured at step b, with a reference value. The present invention also relates to a diagnostic composition comprising or consisting essentially of or consisting of at least one PERV-B.RBD ligand, a variant and/or a fragment thereof, and at least one pharmaceutically acceptable excipient.

As used herein, the term“consisting essentially of’, with reference to a composition, means that the at least one PERV-B.RBD ligand of the invention is the only one diagnostic agent, therapeutic agent or agent with a biologic activity within said composition.

The present invention also relates to a diagnostic composition comprising or consisting essentially of at least one labeled PERV-B.RBD ligand, variant and/or fragment thereof, and at least one pharmaceutically acceptable excipient. As used herein, the term“pharmaceutically acceptable” refers to molecular entities and compositions that do not produce an adverse, allergic or other untoward reaction when administered to a subject, especially a human, as appropriate. Hence,“Pharmaceutically acceptable excipient” refers to molecular entities and compositions that do not produce an adverse, allergic or other untoward reaction when administered to a subject, especially a human, as appropriate. It includes any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents and the like. For human administration, preparations should meet, pyrogenicity, sterility, general safety and purity standards as required by regulatory offices, such as, for example, FDA Office or EMA. A pharmaceutically acceptable carrier or excipient may thus refer to a non-toxic solid, semi-solid or liquid filler, diluent, encapsulating material or formulation auxiliary of any type.

Pharmaceutically acceptable excipients include water, saline, Ringer's solution, dextrose solution, and solutions of ethanol , glucose, sucrose, dextran, mannose, mannitol, sorbitol, polyethylene glycol (PEG), phosphate, acetate, gelatin, collagen, Carbopol®, vegetable oils, and the like. One may additionally include suitable preservatives, stabilizers, antioxidants, antimicrobials, and buffering agents, such as, for example, BHA, BHT, citric acid, ascorbic acid, tetracycline, and the like.

Other examples of pharmaceutically acceptable excipients that may be used in the composition of the invention include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, serum proteins, such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substances, polyethylene glycol, sodium carboxymethylcellulose, polyacrylates, waxes, polyethylene- polyoxypropylene- block polymers, polyethylene glycol and wool fat.

In addition, pharmaceutically acceptable excipients may comprise some excipients, such as, for example, surfactants (e.g. hydroxypropylcellulose); suitable carriers, such as, for example, solvents and dispersion media containing, for example, water, ethanol, polyol (e.g. glycerol, propylene glycol, and liquid polyethylene glycol, and the like), suitable mixtures thereof, and vegetable oils, such as, for example, peanut oil and sesame oil; isotonic agents, such as, for example, sugars or sodium chloride; coating agents, such as, for example, lecithin; agents delaying absorption, such as, for example, aluminum monostearate and gelatin; preservatives, such as, for example, benzalkonium chloride, benzethonium chloride, chlorobutanol, thimerosal and the like; buffers, such as, for example, boric acid, sodium and potassium bicarbonate, sodium and potassium borates, sodium and potassium carbonate, sodium acetate, sodium biphosphate and the like; tonicity agents, such as, for example, dextrose, potassium chloride, propylene glycol, sodium chloride; antioxidants and stabilizers, such as, for example, sodium bisulfite, sodium metabisulfite, sodium thiosulfite, thiourea and the like; nonionic wetting or clarifying agents, such as, for example, polysorbate 80, polysorbate 20, poloxamer 282 and tyloxapol; viscosity modifying agents, such as, for example dextran 40, dextran 70, gelatin, glycerin, hydroxyethylcellulose, hydroxymethylpropylcellulose, lanolin, methylcellulose, petrolatum, polyethylene glycol, polyvinyl alcohol, polyvinylpyrrolidone, carboxymethylcellulose; and the like.

In one embodiment, the diagnostic composition of the invention is for diagnosing a SMVT-related disease, using a method of the invention as described hereinabove.

In one embodiment, the PERV-B.RBD ligand of the invention, variant and/or fragment thereof, is encapsulated.

The techniques of encapsulation are well known in the state of the art. Examples of capsule include, but are not limited to, phospholipids, polymers and liposomes

In one embodiment, the PERV-B.RBD ligand of the invention, variant and/or fragment thereof, is encapsulated with a detectable label. In one embodiment, the in vitro method of the present invention is for assessing the severity of a SMVT-related disease in a subject, or prognosing a SMVT-related disease.

The present invention also relates to a composition comprising or consisting essentially of or consisting of at least one PERV-B.RBD ligand according to the invention, a variant and/or a fragment thereof. The present invention also relates to a pharmaceutical composition comprising or consisting essentially of or consisting of at least one PERV-B.RBD ligand according to the invention, a variant and/or a fragment thereof, and at least one pharmaceutically acceptable excipient.

The present invention also relates to a medicament comprising or consisting essentially of or consisting of at least one PERV-B.RBD ligand according to the invention, a variant and/or a fragment thereof. The present invention also relates to the PERV-B.RBD ligands, variants and or fragments thereof, the pharmaceutical composition or the medicament according to the invention for use in the treatment of an SMVT-related disease.

The present invention also relates to a method for treating an SMVT-related disease, comprising administering to a subject at least one PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, the pharmaceutical composition or the medicament according to the invention.

In one embodiment, a therapeutically effective amount of the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, is administered to the subject. In one embodiment, the administration of a PERV-B.RBD ligand, a variant and/or a fragment thereof, modulates the flux of vitamins through the SMVT receptor.

In one embodiment, the administration of a PERV-B.RBD ligand, a variant and/or a fragment thereof, modulates the flux ofbiotin, pantothenic acid and/or lipoic acid through the SMVT receptor. The present application also relates to a method for targeting cells, samples, tissues, and/or organs expressing SMVT, wherein said method comprises the administration of a PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof. Such method may be used, for example, for targeting therapeutic agents to cells, samples, tissues, and/or organs in a subject in need thereof. In one embodiment, the targeting method of the invention is for targeting anticancer drugs to cancer cells, in particular to SMVT- expressing cancer cells as described herein.

In one embodiment, the PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof, is encapsulated with a therapeutic agent to be specifically administered to cells, samples, tissues or organs of a subject in need thereof. Another object of the present invention is a screening method to identify compounds modulating the level of SMVT, said method comprising the detection and/or measure of the level of SMVT in a biological sample using the in vitro or in vivo methods of the invention. Hence, the present invention further relates to a screening method to identify compounds modulating the level of SMVT, using a PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof comprising the steps of:

a. measuring the level of SMVT in a biological sample from a subject using an in vitro method of the invention;

b. contacting said sample with the tested compound;

c. measuring the level of SMVT in said sample using an in vitro method of the invention; and,

d. comparing the levels of SMVT measured at step a. and c.

The present invention also relates to a screening method to identify compounds modulating the level of SMVT using a PERV-B.RBD ligand of the invention, a variant and/or a fragment thereof comprising the steps of:

a. measuring the level of SMVT in a subject using an in vivo method of the invention;

b. contacting said subject with said compound;

c. measuring the level of SMVT in a subject using an in vivo method of the invention; and,

d. comparing the levels of SMVT measured at step a. and c.

In one embodiment, the methods of the invention further comprise a step of measuring the surface level of at least one other cell surface receptor using an RBD ligand that binds specifically to said at least one other surface receptor.

Example of cell surface receptor-RBD ligands combinations that can be considered for their use with the RBD ligand of th e invention include, without limitation, those disclosed in international patent applications W02010079208 and WO2015110606, GLUT1- human T-cell leukemia virus (HLTV) RBDs (see e.g. international patent application W02004096841), CAT 1 -bovine leukemia virus (BLV) RBDs (see e.g. international patent application WO2017085271), PAR1/RFT3 and PAR2/RFT1 receptor-PERV -A RBD (see e.g. international patent application WO2012035166). In one embodiment, the PERV-B.RBD ligand, a variant and/or a fragment thereof, the composition, the pharmaceutical composition, the medicament or the diagnostic composition of the invention is to be administered at a dose determined by the skilled artisan and personally adapted to each subject. It will be understood that the usage of the PERV-B.RBD ligand, a variant and/or fragment thereof, the composition, the pharmaceutical composition, the medicament or the diagnostic composition of the invention will be decided by the attending physician within the scope of sound medical judgment. The specific effective amount for any particular patient will depend upon a variety of factors including the specific composition employed, the age, body weight, general health, sex and diet of the subject; the time of administration, route of administration, and like factors well known in the medical arts.

In one embodiment, the PERV-B.RBD ligand, a variant and/or a fragment thereof, the composition, the pharmaceutical composition, the medicament or the diagnostic composition of the invention is to be administered by injection, orally, topically, nasally, buccally, rectally, vaginally, intratracheal ly, by endoscopy, transmuco sally, or by percutaneous administration.

In one embodiment, the PERV-B.RBD ligand, a variant and/or a fragment thereof, the composition, the pharmaceutical composition, the medicament or the diagnostic composition of the invention is to be administered by injection, preferably is to be systemically injected. Examples of formulations adapted to systemic injections include, but are not limited to, liquid solutions or suspensions, solid forms suitable for solution in, or suspension in, liquid prior to injection. Examples of systemic injections include, but are not limited to, intravenous, subcutaneous, intramuscular, intradermal, intravitreal, and intraperitoneal injection, or perfusion. In another embodiment, when injected, the PERV- B.RBD ligand, a variant and/or a fragment thereof, the composition, the pharmaceutical composition, the medicament or the diagnostic composition of the invention is sterile. Methods for obtaining a sterile PERV-B.RBD ligand, a variant and/or a fragment thereof, or the diagnostic composition, include, but are not limited to, GMP synthesis (GMP stands for“Good manufacturing practice”). In one embodiment, the PERV-B.RBD ligand, a variant and/or a fragment thereof, the composition, the pharmaceutical composition, the medicament or the diagnostic composition of the invention is to be orally administered. Examples of formulations adapted to oral administration include, but are not limited to, solid forms, liquid forms and gels. Examples of solid forms adapted to oral administration include, but are not limited to, pill, tablet, capsule, soft gelatine capsule, hard gelatine capsule, caplet, compressed tablet, cachet, wafer, sugar-coated pill, sugar coated tablet, or dispersing/or disintegrating tablet, powder, solid forms suitable for solution in, or suspension in, liquid prior to oral administration and effervescent tablet. Examples of liquid forms adapted to oral administration include, but are not limited to, solutions, suspensions, drinkable solutions, elixirs, sealed phial, potion, drench, syrup and liquor.

In another embodiment, the PERV-B.RBD ligand, a variant and/or a fragment thereof, the composition, the pharmaceutical composition, the medicament or the diagnostic composition of the invention is to be topically administered. Examples of formulations adapted to topical administration include, but are not limited to, sticks, waxes, creams, lotions, ointments, balms, gels, masks, leave -on washes and/or the like.

Depending on the cell(s), sample(s), tissue(s) and/or organ(s) targeted, the skilled artisan can determine the technology needed for the introduction of the PERV-B.RBD ligand, a variant and/or fragment thereof, the composition, the pharmaceutical composition, the medicament or the diagnostic composition of the invention in the targeted cell(s), sample(s), tissue(s) and/or organ(s).

In one embodiment, the PERV-B.RBD ligand, a variant and/or a fragment thereof, the composition, the pharmaceutical composition, the medicament or the diagnostic composition of the invention is to be administered in a sustained-release form. In another embodiment, the PERV-B.RBD ligand, a variant and/or a fragment thereof, the composition, the pharmaceutical composition, the medicament or the diagnostic composition of the invention comprises a delivery system that controls the release of the agent.

In one embodiment, the sample is a biological sample. Examples of biological samples include, but are not limited to, body fluids, cell samples, tissue samples, biopsy samples.

In one embodiment, the biological sample is a body fluid. Examples of body fluids include, but are not limited to, blood, plasma, serum, lymph, ascetic fluid, cystic fluid, urine, bile, synovial fluid, bronchoalveolar lavage fluid, sputum, amniotic fluid, peritoneal fluid, cerebrospinal fluid, pleural fluid, pericardial fluid, semen, saliva, sweat and milk.

In one embodiment the biological sample is a tissue sample. Examples of tissues include, but are not limited to, placenta, intestine, brain, liver, lung, kidney, cornea, retina, heart breast, cervix, kidney, pancreas, ovary, skin, nerve, spleen, thymus, esophagus, stomach, testis, hair, skin, bone, uterus, bladder and spinal cord.

In one embodiment, the biological sample is a biopsy sample. In one embodiment, the biological sample is a fine-needle aspirate sample. In one embodiment, the biological sample is a resection sample. In one embodiment, the biological sample is a cell sample. Examples of cell samples include, without being limited to, red blood cells, peripheral blood mononuclear cells (PBMC), peripheral white blood cells, cell samples obtained from tissue biopsies such as lymph nodes biopsies, intestinal or synovial biopsies, or cell sample obtained from broncho-alveolar lavage or cerebrospinal fluid, cell culture sample. In one embodiment, the methods according to the present invention comprise a step of providing a biological sample from a subject.

In one embodiment, the sample was previously taken from the subject, i.e., the in vitro methods of the invention do not comprise a step of recovering a sample from the subject. Consequently, according to this embodiment, the in vitro methods of the invention are non-invasive methods.

It will be understood that the in vivo methods of the invention will be implemented by the attending physician within the scope of sound medical judgment. The specific implementation of the in vivo methods of the invention for any particular subject will depend upon a variety of factors including the condition being considered, the predisposition the said condition, the age, body weight, general health, sex and diet of the subject; and like factors well known in the medical arts.

Another object of the present invention is a kit for implementing the methods of the invention, wherein said kit comprises at least one PERV-B.RBD ligand of the invention, a variant and/or fragment thereof.

In one embodiment, the kit of the invention further comprises cells displaying SMVT at the cell surface for use as a reference.

The present invention further relates to a method for the treatment of cancer in a subject, preferably of a SMVT -related cancer, more preferably of a cancer selected from the group consisting of liver cancer, prostate cancer, lung cancer, gallbladder cancer, pancreas cancer, colon cancer, ovarian cancer, brain cancer, kidney cancer, thyroid cancer, lymphomas, urothelial cancer, cervical cancer and endometrial cancer, comprising the steps of:

a) diagnosing said cancer using an in vitro or in vivo method according to the invention for diagnosing a SMVT -related disease,

b) treating said cancer, preferably by chemotherapy.

Examples of chemotherapies include, but are not limited to:

a. alkylating agents that act mainly by forming covalent bonds between DNA bases, including, but not limited to, nitrogen mustards ( e.g ., cyclophosphamide), aziridines and epoxides (e.g., thiopeta), alkyl sulfonates (e.g., busulfan), nitrosureas (e.g., BCNU and CCNU), hydrazine and triazine derivatives (e.g., procarbazine and temozolomide);

b. cisplatin and its analogs that act by forming DNA adducts which lead to intra strand and inter-strand linking leading to the formation of DNA filaments, including, but not limited to, carboplatin, cisplatin and oxaliplatin;

c. antimetabolites including but not limited to folate metabolism inhibitors (e.g., methotrexate, trimetrexate, tomudex), 5 -fluoropyrimidines (e.g., 5-FU), oral fluoropyramidines ( e.g ., tegafur, uracil, capecitabine), necleoside analogs ( e.g ., cytarabine), gemcitabine and 6-thiopurines (e.g., 6-MP and 6-TG);

d. topoisomerase-interactive agents that affect the topologic states of DNA by interfering or modulating DNA cleavage, strand passage and re-ligation, including, but not limited to, epipodophyllotoxins (e.g., etoposide and teniposide), camptothecin analogs, anthracyclines (e.g., doxorubicin, daunorubicin, epirubicin, idarubicin), mitoxantrone and losoxantrone, and dactinomycin;

e. antimicrotubule agents, which interfere with the proper polymerization/ depolymerization of microtubules, including, but not limited to, vinca alkaloids (e.g., vincristine, vinorelbine and vinblastine), taxanes (e.g., paclitaxel, docetaxel) and estramustine phosphate; and

f. numerous miscellaneous agents exist which cannot be classified into any of the above groups, including but not limited to suramin, bleomycin, L-asparaginase and amifostine. The present invention further relates to a method for the treatment of diseases characterized by a lower expression and/or function of SMVT in a subject, comprising the steps of:

a) diagnosing said disease using an in vitro or in vivo method according to the invention for diagnosing a SMVT -related disease;

b) treating said disease, preferably by a biotin, pantothenic acid and/or lipoic acid supplementation.

BRIEF DESCRIPTION OF THE DRAWINGS

Figure 1 is a plot showing a representative example of the result of three independent automated screenings identifying SLC5A6/SMVT as the PERV-B.RBD cognate receptor among 172 soluble carrier family member. The fluorescence intensity (y-axis - positively correlating with the binding of PERV-B.RBD) is plotted for each of the SEC receptor tested (x-axis). Figure 2 is a set of graphs showing the specific PERV-B.RBD binding to SLC5A6/SMVT. A) HEK 293T cells were transfected with empty vector (pCHIX), a SMVT expression or a glucose transporter type 1 (GLUT-l) expression vector. B) HEK 293T cells were transfected with siRNAs directed against luciferase (siLUC, upper panels), SMYT (siSMVT) alone (central panels) or in combination with SMVT expression vector (siSMVT+SMVT, lower panels). SMVT expression level was monitored using PERV-B.RBD ligand (and GLUT-l expression using human T-cell leukemia virus type 2 (HTLV2)-RBD (H2-RBD) by flow cytometry. Nonspecific staining (filled histograms) and specific binding (solid line histograms) are represented. The number of cells (count - y-axis) is plotted as a function of the fluorescence intensity (AU - x-axis). Relative specific binding of each RDB in the different conditions, expressed as the delta of the geometric mean of the fluorescence intensity between a specific binding and a nonspecific staining, is indicated in the upper right of each panel.

Figure 3 is a set of graphs confirming the specific PERV-B.RBD binding to SLC5A6/SMVT using a second siSMVT siRNA. HEK 293T cells were transfected with either a siLUC control siRNA (siLUC) (upper panel), or an anti- SMVT siRNA (siSMVT) (lower panel). Variation of relative binding of different RBD ligands was compared by flow cytometry in these two conditions. RBD ligands included a control supernatant preparation with no RBD (MOCK), or a preparation of either PERV-B.RBD (PERV-B), or a RBD from a xenotropic murine retrovirus (XRBD), whose receptor is known to be XPR1/SLC53A1, or the HTLV2-RBD (H2), whose receptor is known to be GLUT1/SLC2A1, or a RBD derived from the bovine leukemia virus (BLV), whose receptor is known to be CAT1/SLC7A1. The number of cells (count - y-axis) is plotted as a function of the fluorescence intensity (AU - x-axis).

EXAMPLES

The present invention is further illustrated by the following examples. Example 1: PERVB-RBD automated screen identifies SLC5A6 as the PERVB-RBD cognate receptor

Materials and Methods

Three independent screenings for PERV-B-RBD (SEQ ID NO: 13) binding on a collection of 172 member of the Solute Carrier protein (SLC) family were performed with a Freedom-EVO ^® robot from Tecan with acquisition of images and fluorescence intensity parameters by Cellomics (Array Scan XTI HCS Thermo Scientific).

20 000 quail QT6 cells per well were seeded in a 96 well plate coated with poly-D-lysine. 24 hours later, cells were transfected with 100 ng of SLC expression vectors using JetPrime transfection reagent (Polypus Transfection 114-15) according to the manufacturer’s instructions. QT6 cell were chosen as the spontaneous binding of the PERY-B.RBD ligand was the lowest among the cell lines considered and tested. Cells were washed the next day with PBS and incubated in fresh DMEM/FBS for 48 hours before binding assays. Binding assays were performed on transfected adherent cells that were washed with PBA (PBS with 2% FBS), incubated in 40m1 with either a saturating concentration of the PERV-B RBD ligand fused to a mouse Fc fragment (SEQ ID NO: 13), or a control supernatant, or a control RBD known to interact with a cognate SLC protein. Incubation was carried on for 30 min at 37°C, before cells were washed twice with PBA, incubated with Alexa488-conjugated (Invitrogen) anti-mouse IgGl antibody (1/500 dilution) at room temperature, washed twice with PBA and fixed with 1% paraformaldehyde (PFA). Transfection and binding assays were performed on the Freedom EVO robot (Tecan). Images and fluorescence intensity parameters were acquired by Cellomics (Array Scan XTI HCS, Thermo Scientific). Fluorescent signal was analyzed using GraphPad Prism 5. Results and conclusions

Among the collection of members of the Solute carrier (SLC) protein family, PERV- B.RBD ligand binds to SMVT/SLC5A6 (Fig. 1). Example 2: Specificity of the binding of PER V-B. RBD ligand to SMVT/SLC5A6

Material and methods

5xl0 ⁵ HEK293T cells were seeded on a 6-well plate and transfected with a siRNA directed either against the firefly luciferase gene (siLUC, 5’- CUUACGCUGAGUACUUCGA-3’ - SEQ ID NO: 15), or a siRNA directed against the

SLC5A6 gene (siSMVT, 5’ -GGAUGAGUCUUGGUGUGUUTT-3’ - SEQ ID NO: 16). Forty-eight hours post-transfection, cells were detached with lmM EDTA in PBS. For the binding assay, lxl(P cells were resuspended in IOOmI of PBA (PBS with 2%FBS) containing a saturating concentration of either the PERV-B.RBD (SEQ ID NO: 13), or the human T-cell leukemia virus type 2 (HTLV 2)-RBD known to bind SLC2A 1 / GLUT 1 , and incubated at 37°C for 30min. Cells were then washed twice with IOOmI of PBA, incubated with Alexa488 -congugated anti-mouse IgGl at 4°C for 20min, washed twice and resuspended in 200m1 of PBA. The results were acquired by flow cytometry on a FACSCalibur (Becton Dickinson) and analyzed by FlowJo. Nonspecific staining with no RBD (filled histograms) and specific binding of the RBD (solid line histograms) are represented as delta of the geometric mean of the fluorescence intensity between a specific binding and a nonspecific staining. HEK 293T cells were transfected as above with either the empty vector (pCHIX,“vecteur vide”), the SMVT expression vector (SMVT), or the GLUT-l expression vector. All were tested with PERV-B.RBD (SEQ ID NO: 13) or HTLV2-RBD, the latter known to bind SLC2A1/GLUT1.

Results and conclusion

The binding of the PERV-B.RBD ligand increased specifically when cells overexpressed SMVT (Fig. 2A) and decreased specifically in cell underexpressing SMVT (Fig. 2B). The PERV-B.RBD thus binds specifically to SMVT/SLC5A6, allowing it use in the diagnosis of disease characterized by a variation of SMVT expression. Example 3: Specificity of the binding of PER V-B.RBD ligand to SMVT/SLC5A 6, as assessed with a second anti-SMVT siRNA

Material and methods

5xl0 ⁵ HEK293T cells were seeded on a 6-well plate and transfected with a siRNA directed either against the firefly luciferase gene (siLUC, 5’- CUUACGCUGAGUACUUCGA-3’ - SEQ ID NO: 15), or a siRNA directed against the SLC5A6 gene and different from the siRNA used in Example 2 (siSMVT A, 5’ GCAGGAUCAUGCCAGAAAUTT-3’ - SEQ ID NO: 23). Forty-eight hours post transfection, cells were detached with lmM EDTA in PBS. For the binding assay, lxlO ⁵ cells were resuspended in IOOmI of PBA (PBS with 2%FBS) containing a predetermined saturating concentration of either the PERV-B.RBD (SEQ ID NO: 13), or a RBD from a xenotropic murine retrovirus (XRBD), whose receptor is known to be XPR1/SLC53A1, or the HTLV2-RBD (H2), whose receptor is known to be GLUT1/SLC2A1, or a RBD derived from the bovine leukemia virus (BLY), whose receptor is known to be CAT1/SLC7A1, or a control supernatant preparation with no RBD (MOCK), followed by an incubation at 37°C for 30min. All RBD were produced as fusion proteins with mFC (PERV-B.RBD, XRBD, BLV-RBD and HTLY2-RBD). Cells were then washed twice with IOOmI of PBA, incubated with Alexa488 -congugated anti-mouse IgGl at 4°C for 20min, and washed twice and resuspended in 200m1 of PBA. The results were acquired by flow cytometry on a FACSCalibur (Becton Dickinson) and analyzed by FlowJo. Relative specific binding of each RDB in the different conditions, expressed as the delta of the geometric mean of the fluorescence intensity between a specific binding and a nonspecific staining.

Results and conclusion Specific binding of the PERV-B.RBD ligand decreased significantly when cells where treated with anti-SMVT siRNA, with a drop of over 2-fold (77.5 to 34, Fig. 3 and table 1). Specific drop of PERV-B.RBD binding observed upon introduction of siSMVT was assessed as binding of XRBD, H2-RBD or BLV-RBD did not vary significantly between siLUC (Fig.3 left panel) and siSMVT treatment (Fig. 3 right panel). This confirmed that PERV-B.RBD binds specifically to SMVT/SLC5A6, allowing it use in the diagnosis of disease characterized by a variation of SMYT expression.

Table 1: Relative binding of each RBD preparation and the control (MOCK) is expressed Relative specific binding of each RDB in the different conditions, expressed as the delta of the geometric mean of the fluorescence intensity between a specific binding and a nonspecific staining.

Example 4: PERV-B.RBD ligand allows the detection of variations of the expression ofSMVT at the surface of cancer cells.

Materials and Methods For the binding assay, lxlO ⁵ cells of each cell type were resuspended in IOOmI of PBA (cell density of lxlO ⁶ per mL) containing a saturating concentration of either the PERV- B-RBD (SEQ ID NO: 13), and incubated at 37°C for 30min. Cells were washed twice with IOOmI of PBA, incubated with PE-conjugated anti-mouse IgGl at 4°C for 20min, washed twice and resuspended in 200m1 of PBA. The results were acquired by flow cytometry on a FACSverse (Becton Dickinson) and analyzed with the FlowJo software (FLOWJO, EEC). Relative specific binding of PERV-B.RBD to the different cells is expressed as the delta of the geometric mean of the fluorescence intensity between a specific binding and a nonspecific staining.

Results and conclusions The binding of PERV-B.RBD to the surface of the cells was expressed in terms of the mean signal to noise ratio, for each cell type. Most cancer cell lines displayed a signal to noise ratio over 100 (table 2).

The results indicate that variations of expression level of SMVT, are indicative of cancer. Table 2: Expression of SMVT in different human cancer cell lines. Bold font distinguishes cells of cancerous origin. Relative specific binding of PERV-B.RBD to the different cells is expressed as the delta of the geometric mean of the fluorescence intensity between a specific binding and a nonspecific staining.