NZ787569A - Antibodies useful in cancer diagnosis - Google Patents

Abstract

The invention relates to antibodies directed against an epitope located within the C-terminal portion of CLDN6 which are useful, for example, in diagnosing cancer and/or in determining whether cancer cells express CLDN6.

Description

Antibodies useful in cancer diagnosis This application is a divisional of New d patent application number 761712, the entire content of which is incorporated herein by this cross-reference.

Claudins are integral membrane proteins located within the tight junctions of epithelia and endothelia. Claudins are predicted to have four transmembrane segments with two extracellular loops, and N- and C-termini located in the cytoplasm. The n (CLDN) family of transmembrane proteins plays a critical role in the nance of epithelial and endothelial tight junctions and might also play a role in the maintenance of the cytoskeleton and in cell signaling.

Claudin-6 (CLDN6) is an oncofetal gene expressed in murine and human stem cells as well as embryoid bodies committed to the epithelia cell fate (Turksen, K. et al. (2001) Dev Dyn 222, 292—300; Anderson WJ. et al. (2008) Dev Dyn 237, 504-12; Turksen K. et al. (2002) Development, 129, 4; Assou S. et al. (2007) Stem Cells 25, 961—73). As a tumor-associated antigen it can be classified as a differentiation antigen due to its expression during early stage of epidermal morphogenesis where it is crucial for epidermal differentiation and barrier formation. Additionally expression was observed 2O in epithelial tissues or neonatal normal epithelial tissue of tongue, skin, h and breast za G. et al. (2006), Am J Physiol Renal Physiol 291, 1132—1141; Troy T.C. et al. (2007), Molecular Biotechnology 36, 166-74; Zhao L. et al. (2008), Am] Physiol Regul Integr Comp Physiol 294, 1856—1862). s that, own data also reveal low or very low expression of CLDN6 in human placenta, urinary bladder, endometrium, te and the peripheral nerve and nt overexpression of CLDN6 in different cancers. CLDN6 has been demonstrated to be overexpressed in tumors, including pediatric brain tumors, c adenocarcinomas and germ cell tumors as well as visceral carcinomas such as ovarian carcinomas. It has also been demonstrated that overexpression of CLDN6 in gastric cancer cells results in increased invasiveness, migration and proliferation suggesting that CLDN6 is a marker for poor prognosis and may play a potential role in maintaining the malignant phenotype. In addition, it has been shown that CLDN6 functions as cancer suppressor via inhibition of cell proliferation and induction of apoptosis in breast cancer cell lines. ._ 2 _ The sequence alignment of CLDN3, CLDN4, CLDN6 and CLDN9 shown in Fig. 18 rates that there is a high degree of conservation of CLDN6 to other claudin proteins. This high homology of CLDN6 with other claudin ns, in particular CLDN9 and CLDN4, render it difficult to provide CLDN6 antibodies which have properties such as specificity and affinity suitable for diagnostic purposes. The present inventors found that antibodies directed against a certain epitope located within the C—terminal portion of CLDN6 fulfill the criteria for the diagnostic applicability of antibodies, in particular for detecting and identifying cells expressing CLDN6.

The antibodies of the invention are , for example, in diagnosing cancer and/or in determining whether cancer cells express CLDN6. Preferably, a cancer disease or a cancer cell is characterized by surface expression of CLDN6. Cancer cells expressing CLDN6 are suitable targets for therapies targeting CLDN6 such as therapy with antibodies directed against CLDN6. In one embodiment, cancer cells s or aberrantly express CLDN6 while the corresponding normal cells do not express CLDN6 or s CLDN5 at a lower level.

Summary of the invention In one aspect, the present invention s to an an antibody or antigen—binding fragment f, which binds: (i) to a peptide having the amino acid sequence EYPTKNY (SEQ ID NO: 38), and/or (ii) to claudin 6 (CLDN6), n said dy or antigen-binding fragment thereof binds to CLDN6 by binding at least to an epitope within CLDN6 having the amino acid sequence EYPTKNY (SEQ ID NO: 38), and/or (iii) to a peptide having the amino acid sequence EYPTKNYV (SEQ ID NO: 29), and/or (iv) to n 6 (CLDN6), wherein said antibody or antigen—binding fragment thereof binds to CLDN6 by binding at least to an epitope within CLDN6 having the amino acid sequence EYPTKNYV (SEQ ID NO: 29), and/or _ 3 _ (v) to a peptide having the amino acid sequence AISRGPSEYPTKNYV (SEQ lD NO: 15), wherein the antibody or antigen-binding fragment thereof does not bind to a peptide having the amino acid sequence TSAPAISRGPSEYPT (SEQ ID NO: 14), and/or (vi) to claudin 6 (CLDN6), n said antibody or antigen-binding fragment thereof binds to CLDN6 by binding at least to an epitope within CLDN6 having the amino acid ce AISRGPSEYPTKNYV (SEQ ID NO: 15), wherein the antibody or antigen- binding fragment thereof does not bind to a peptide having the amino acid sequence TSAPAISRGPSEYPT (SEQ ID NO: 14).

In embodiments of s described herein and in further aspects, the present invention s to a monoclonal antibody or antigen-binding fragment thereof which (i) binds to a peptide having the amino acid sequence AISRGPSEYPTKNYV (SEQ lD NO: 15) and/or (ii) binds to claudin 6 (CLDN6), wherein said antibody or antigen-binding fragment thereof binds to CLDN6 by binding at least to an epitope within CLDN6 having the amino acid sequence AISRGPSEYPTKNYV (SEQ ID NO: 15), In embodiments of aspects described herein and in further aspects, the present invention s to an antibody or antigen—binding fragment thereof, which binds to one or more, preferably all, of the following peptides: PAISRGPSEYPTKNY (SEQ ID NO: 22), AISRGPSEYPTKNYV (SEQ ID NO: 15), ISRGPSEYPTKNYV (SEQ ID NO: 23), SRGPSEYPTKNYV (SEQ ID NO: 24), RGPSEYPTKNYV (SEQ ID NO: 25), TKNYV (SEQ lD NO: 26), PSEYPTKNYV (SEQ ID NO: 27), SEYPTKNYV (SEQ lD NO: 28), and YV (SEQ ID NO: 29), wherein the antibody or antigen-binding fragment thereof does not bind to a peptide having the amino acid sequence TSAPAISRGPSEYPT (SEQ ID NO: 14). in one embodiment, the ence in binding affinity to the peptide to which the antibody or n binding fragment binds with the lowest affinity and to the peptide 3O to which the dy or antigen binding fragment binds with the highest affinity is 50% or less, 40% or less, 30% or less, 20% or less, or 10% or less. - 4 _ Antibodies or antigen-binding fragments described herein preferably do not bind to a peptide comprising the amino acid sequence EYPTK (SEQ ID NO: 59) and/or the amino acid sequence EYPTKN (SEQ ID NO: 60) but not comprising the amino acid sequence EYPTKNY (SEQ ID NO: 38). In other words, an antibody or antigen-binding fragment described herein which binds to a peptide having the amino acid sequence Y (SEQ ID NO: 38) and/or a peptide having the amino acid sequence EYPTKNYV (SEQ ID NO: 29) binds to said peptide(s) due to the presence of the second tyrosine which is missing in the amino acid sequence EYPTK (SEQ ID NO: 59) and/or the amino acid sequence EYPTKN (SEQ ID NO: 60). As shown herein, preferred antibodies or antigen- binding fragments do not bind to a peptide sing the amino acid ce YPTKNY (SEQ ID NO: 61) and/or EYPTKN (SEQ ID NO: 60) but not comprising the amino acid sequence EYPTKNY (SEQ ID NO: 38) suggesting that the amino acid sequence EYPTKNY (SEQ ID NO: 38) is a sequence that can be considered to be a minimal epitope for binding of these antibodies.

In ments of aspects described herein and in further s, the present ion relates to an antibody produced by or obtainable from a hybridoma deposited at the DSMZ fenstr. 73, 38124 Braunschweig, y) and having one of the following designations and accession numbers: 1. 58—4B—2, sion no. DSM ACC3311, deposited on November 29, 2016; 2. 58-3A, sion no. DSM ACC3312, deposited on November 29, 2016; or 3. 58—lB, accesssion no. DSM ACC3313, deposited on November 29, 2016.

Antibodies of the invention are designated herein by referring to the designation of the antibody and/or by referring to the clone producing the antibody.

The present invention also relates to an antibody which competes for CLDN6 binding with an antibody produced by and obtainable from the above-described hybridomas and/or has the specificity for CLDN6 of an antibody produced by or obtainable from the above-described hybridomas. In these and other embodiment, the present invention also relates to an antibody comprising an antigen binding n or antigen binding site, in particular a variable region, identical or highly homologous to that of the antibodies _ 5 _ ed by or obtainable from the described omas. it is contemplated that preferred antibodies are those having CDR regions either cal or highly homologous to the CDR regions of antibodies produced by or obtainable from the above-described hybridomas. By "highly homologous" it is plated that from 1 to , preferably from 1 to 4, such as 1 to 3 or 1 or 2 substitutions may be made in each CDR region. Particularly preferred antibodies are the chimerized and humanized forms ofthe antibodies produced by or obtainable from the above-described hybridomas. ingly, in embodiments of aspects described herein and in further aspects, the t invention relates to an antibody ed from the group consisting of: (i) an antibody produced by or able from a clone deposited under the accession no. DSM ACC3313 (58-13), DSM ACC3312 (58-3A) or DSM ACC3311 (58—48-2), (ii) an antibody which is a chimerized or humanized form of the antibody under (i), (iii) an antibody which competes for CLDN6 binding with an antibody under (i), (iv) an dy which has the specificity of the antibody under (i), (v) an antibody comprising the antigen g portion or antigen binding site of the antibody under (i), or an antigen-binding fragment of the antibody under any one of (i) to (v).

In one embodiment, the antigen binding portion or antigen binding site of the antibody under (i) comprises the variable region of the antibody under (i).

In embodiments of aspects described herein and in further aspects, the present invention relates to an antibody selected from the group consisting of: (a) an antibody comprising: an antibody heavy chain comprising: (i) an antibody heavy chain sequence comprising the sequence according to SEQ ID NO: 40, 42, or 44, or a variant thereof, (ii) at least one, preferably two, more preferably all three of the CDR sequences of an antibody heavy chain sequence comprising the sequence according to SEQ ID NO: 40, 42, or 44, or a variant thereof, or _ 5 _ (iii) a CDR3 sequence according to SEQ ID NO: 53 or a variant thereof and preferably further comprising a CDRl sequence according to SEQ ID NO: 51 or 57, or a variant thereof and/or a CDR2 ce according to SEQ ID NO: 52 or 58, or a variant thereof, (b) an antibody which competes for CLDN6 g with an antibody according to (a) and/or has the specificity for CLDN6 of an antibody according to (a), or an antigen-binding fragment of said antibody.

In embodiments of s described herein and in further aspects, the present invention relates to an antibody selected from the group consisting of: (a) an antibody comprising: an dy light chain comprising: (i) an antibody light chain sequence comprising the sequence according to SEQ ID NO: 41, 43, or 45, or a variant thereof, (ii) at least one, preferably two, more preferably all three of the CDR sequences of an antibody light chain sequence comprising the sequence according to SEQ ID NO: 41, 43, or 45, or a variant thereof, or (iii) a CDR3 sequence according to SEQ ID NO: 56 or a variant thereof and preferably further comprising a CDRl sequence according to SEQ ID NO: 54, or a t thereof and/or a CDRZ sequence ing to SEQ ID NO: 55, or a variant thereof, and (b) an dy which competes for CLDN6 binding with an antibody according to (3) and/or has the icity for CLDN6 of an antibody according to (a), or an antigen-binding nt of said antibody.

In ments of aspects described herein and in further aspects, the present invention relates to an antibody selected from the group consisting of: (a) an antibody comprising: (I) an antibody heavy chain comprising: (i) an antibody heavy chain sequence comprising the sequence according to SEQ ID NO: 40, 42, or 44, or a variant thereof, _ 7 _ (ii) at least one, ably two, more preferably all three of the CDR sequences of an antibody heavy chain sequence comprising the sequence according to SEQ ID NO: 40, 42, or 44, or a variant thereof, or (iii) a CDR3 sequence according to SEQ ID NO: 53 or a variant thereof and preferably further sing a CDR1 sequence according to SEQ ID NO: 51 or 57, or a variant thereof and/or a CDR2 sequence according to SEQ ID NO: 52 or 58, or a variant thereof, and/or (II) an antibody light chain comprising: (i) an antibody light chain sequence comprising the sequence according to SEQ ID NO: 41, 43, or 45, or a variant thereof, (ii) at least one, preferably two, more preferably all three of the CDR ces of an antibody light chain sequence comprising the sequence according to SEQ ID NO: 41, 43, or 45, or a variant thereof, or (iii) a CDR3 sequence according to SEQ ID NO: 56 or a variant thereof and preferably further comprising a CDR1 sequence according to SEQ ID NO: 54, or a variant thereof and/or a CDR2 sequence according to SEQ ID NO: 55, or a variant thereof, and (b) an dy which competes for CLDN6 binding with an antibody ing to (a) and/or has the specificity for CLDN6 of an antibody according to (a), or an antigen—binding fragment of said antibody.

In certain preferred embodiments, the present invention relates to an antibody selected from the group consisting of: (a) an antibody comprising: (I) an antibody heavy chain comprising: (i) an antibody heavy chain sequence comprising the sequence according to SEQ ID NO: 40, or a t thereof, (ii) at least one, ably two, more ably all three of the CDR sequences of an antibody heavy chain sequence comprising the ce according to SEQ ID NO: 40, or a variant thereof, or 3O (iii) a CDR3 sequence according to SEQ ID NO: 53 or a variant thereof and preferably further comprising a CDR1 sequence ing to SEQ ID NO: 51, or a variant thereof and/or a CDR2 sequence according to SEQ ID NO: 52, or a variant thereof, and (II) an antibody light chain sing: (i) an antibody light chain sequence comprising the sequence according to SEQ ID NO: 41, or a variant thereof, (ii) at least one, ably two, more preferably all three of the CDR sequences of an antibody light chain sequence comprising the ce according to SEQ ID NO: 41, or a variant thereof, or (iii) a CDR3 sequence according to SEQ ID NO: 56 or a variant thereof and preferably further comprising a CDR1 sequence according to SEQ ID NO: 54, or a variant thereof and/or a CDR2 sequence according to SEQ ID NO: 55, or a variant thereof, and (b) an antibody which competes for CLDN6 g with an antibody according to (a) and/or has the specificity for CLDN6 of an antibody according to (a), or an antigen—binding fragment of said antibody.

In certain preferred embodiments, the present invention relates to an antibody selected from the group consisting of: (a) an antibody comprising: (I) an dy heavy chain comprising: (i) an antibody heavy chain sequence comprising the sequence according to SEQ ID NO: 42, or a variant thereof, (ii) at least one, preferably two, more ably all three of the CDR ces of an antibody heavy chain sequence sing the ce according to SEQ ID NO: 42, or a variant thereof, or (iii) a CDR3 sequence according to SEQ ID NO: 53 or a variant thereof and preferably further comprising a CDR1 sequence according to SEQ ID NO: 57, or a variant f and/or a CDR2 sequence according to SEQ ID NO: 58, or a variant thereof, and (II) an antibody light chain comprising: (i) an antibody light chain sequence comprising the sequence according to SEQ ID NO: 43, or a variant thereof, (ii) at least one, preferably two, more preferably alE three of the CDR sequences of an antibody light chain sequence comprising the sequence according to SEQ ID NO: 43, or a variant thereof, or _ 9 - (iii) a CDR3 sequence according to SEQ ID NO: 56 or a variant thereof and preferably further comprising a CDR1 sequence according to SEQ ID NO: 54, or a variant f and/or a CDRZ sequence according to SEQ ID NO: 55, or a variant thereof, and (b) an antibody which competes for CLDN6 binding with an antibody according to (3) and/or has the specificity for CLDN6 of an antibody according to (a), or an antigen-binding fragment of said antibody.

In certain red embodiments, the present invention s to an antibody selected from the group consisting of: (a) an antibody sing: (I) an antibody heavy chain comprising: (i) an antibody heavy chain sequence comprising the sequence according to SEQ ID NO: 44, or a variant thereof, (ii) at least one, preferably two, more preferably all three of the CDR sequences of an antibody heavy chain ce comprising the sequence according to SEQ ID NO: 44, or a variant thereof, or (iii) a CDR3 sequence according to SEQ ID NO: 53 or a variant thereof and preferably r comprising a CDR1 sequence according to SEQ ID NO: 57, or a variant f and/or a CDRZ sequence according to SEQ ID NO: 58, or a variant thereof, and (II) an antibody light chain comprising: (i) an antibody light chain sequence comprising the sequence according to SEQ ID NO: 45, or a variant thereof, (ii) at least one, preferably two, more preferably all three of the CDR sequences of an antibody light chain sequence comprising the sequence according to SEQ ID NO: 45, or a variant thereof, or (iii) a CDR3 sequence according to SEQ iD NO: 56 or a variant f and ably further comprising a CDR1 ce according to SEQ ID NO: 54, or a variant thereof and/or a CDR2 sequence according to SEQ ID NO: 55, or a variant thereof, and (b) an antibody which competes for CLDN6 binding with an antibody according to (a) 3O and/or has the specificity for CLDN6 of an antibody according to (a), or an antigen-binding fragment of said antibody. _ 10 _ In n red embodiments, the present invention relates to an antibody selected from the group ting of: (a) an antibody comprising an antibody heavy chain comprising a CDR3 sequence according to SEQ ID NO: 53 or a variant thereof and an antibody light chain comprising a CDR3 sequence ing to SEQ ID NO: 56 or a variant f, and (b) an dy which competes for CLDN6 binding with an antibody according to (a) and/or has the specificity for CLDN6 of an antibody according to (a), or an antigen—binding fragment of said antibody.

In certain preferred ments, the present invention relates to an antibody ed from the group consisting of: (a) an antibody comprising an antibody heavy chain comprising a CDR3 sequence ing to SEQ ID NO: 53 or a variant thereof and further comprising a CDR1 sequence according to SEQ ID NO: 51, or a variant thereof and a CDR2 sequence according to SEQ ID NO: 52, or a variant thereof, and an antibody light chain comprising a CDR3 sequence according to SEQ ID NO: 56 or a variant thereof and further comprising a CDR1 ce according to SEQ ID NO: 54, or a variant thereof and a CDR2 sequence according to SEQ ID NO: 55, or a variant thereof, and (b) an antibody which competes for CLDN6 binding with an antibody according to (a) and/or has the icity for CLDN6 of an antibody according to (a), or an antigen-binding fragment of said antibody.

In certain preferred embodiments, the present invention relates to an antibody selected from the group ting of: (a) an antibody comprising an antibody heavy chain comprising a CDR3 sequence according to SEQ ID NO: 53 or a variant thereof and further comprising a CDR1 sequence according to SEQ ID NO: 57, or a variant thereof and a CDR2 sequence according to SEQ ID NO: 58, or a variant thereof, and an antibody light chain comprising a CDR3 sequence according to SEQ ID NO: 56 or a variant thereof and further comprising a CDR1 sequence according to SEQ ID NO: 54, or a variant thereof and a CDR2 sequence according to SEQ ID NO: 55, or a variant thereof, and _ 11 _ (b) an antibody which competes for CLDN6 binding with an antibody according to (a) and/or has the specificity for CLDN6 of an antibody according to (a), or an antigen-binding nt of said antibody.

In certain preferred embodiments, the t invention relates to an antibody ed from the group consisting of: (a) an antibody comprising a heavy chain variable region (VH) comprising an amino acid sequence represented by SEQ ID NO: 40 or a variant thereof and a light chain variable region (VL) comprising an amino acid sequence represented by SEQ ID NO: 41 or a variant thereof, and (b) an antibody which competes for CLDN6 binding with an antibody ing to (a) and/or has the specificity for CLDN6 of an dy according to (a), or an antigen-binding fragment of said antibody. in certain preferred embodiments, the present invention s to an antibody selected from the group consisting of: (a) an antibody comprising a heavy chain variable region (VH) comprising an amino acid ce represented by SEQ ID NO: 42 or a t thereof and a light chain variable region (VL) comprising an amino acid sequence represented by SEQ ID NO: 43 or a variant thereof, and (b) an antibody which competes for CLDN6 binding with an antibody according to (a) and/or has the specificity for CLDN6 of an antibody according to (a), or an n—binding fragment of said antibody.

In n preferred embodiments, the present invention relates to an antibody selected from the group consisting of: (a) an antibody sing a heavy chain variable region (VH) comprising an amino acid sequence represented by SEQ ID NO: 44 or a variant thereof and a light chain variable region (VL) comprising an amino acid sequence represented by SEQ ID NO: 45 or a 3O variant thereof, and (b) an antibody which competes for CLDN6 binding with an antibody according to (a) and/or has the specificity for CLDN6 of an antibody according to (a), "12.. or an antigen-binding fragment of said antibody.

In preferred embodiments, an antibody of the invention comprises an antibody heavy chain sing a gamma-2a heavy chain constant region, preferably a human gamma- 2a heavy chain constant region and/or comprises an antibody light chain comprising a kappa light chain constant region.

The antibodies or antigen—binding fragments described herein bind to CLDN6. An antibody or antigen-binding nt of the invention is preferably able to bind to CLDN6 in its native, i.e. naturally occurring or non-denatured state, or in its denatured state. In one embodiment, an antibody or antigen—binding fragment thereof of the invention binds to CLDN6 but not to CLDN9 and preferably does not bind to CLDN4 and/or CLDN3. Preferably, an antibody or n-binding fragment thereof of the invention does not substantially bind to a CLDN protein other than CLDN6. Preferably, an antibody or antigen—binding fragment thereof of the ion is specific for CLDN6.

In one embodiment, CLDN6 is cell e membrane-bound CLDN6. In one embodiment, CLDN6 is present on cancer cells, n said cancer cells are preferably CLDN6 expressing cancer cells. In one embodiment, said cancer cells are cells from a cancer selected from the group ting of ovarian cancer, in particular ovarian adenocarcinoma and ovarian teratocarcinoma, lung cancer, including small cell lung cancer (SCLC) and non—small cell lung cancer (NSCLC), in particular squamous cell lung carcinoma and adenocarcinoma, gastric cancer, breast cancer, hepatic cancer, pancreatic cancer, skin cancer, in particular basal cell carcinoma and squamous cell carcinoma, malignant melanoma, head and neck cancer, in particular malignant pleomorphic a, sarcoma, in particular synovial sarcoma and carcinosarcoma, bile duct cancer, cancer of the urinary bladder, in particular transitional cell carcinoma and papillary carcinoma, kidney cancer, in particular renal cell carcinoma including clear cell renal cell carcinoma and papillary renal cell oma, colon , small bowel 3O cancer, including cancer of the ileum, in particular small bowel adenocarcinoma and adenocarcinoma of the ileum, testicular nal carcinoma, placental choriocarcinoma, cervical cancer, ular , in particular testicular seminoma, __ 13 _ testicular teratoma and embryonic testicular , uterine cancer, germ cell tumors such as a teratocarcinoma or an embryonal carcinoma, in particular germ cell tumors of the testis, and the metastatic forms thereof. in one embodiment, an antibody of the invention is a chimeric, human or humanized antibody. In one embodiment, an antibody of the invention is a monoclonal antibody. in one embodiment, an antibody of the ion is obtainable by a method comprising the step of immunizing an animal with a peptide comprising, preferably consisting ofthe amino acid sequence of SEQ ID NO: 49, or an immunologically equivalent peptide, or a nucleic acid or host cell expressing said peptide. Preferably said peptide comprises not more than 110, 100, 90, 80, 70, 60, 50, or 40 contiguous amino acids of CLDN6.

Antibodies or antigen~binding fragments ofthe invention may be d, i.e. covalently or valently linked, to other moieties such as able labels. in a further aspect, the present invention s to a conjugate comprising an antibody or antigen—binding fragment described herein d to at least one detectable label.

The t invention also relates to a cell such as a hybridoma producing an antibody as described herein.

Preferred hybridomas are those deposited at the DSMZ (lnhoffenstr. 73, 38124 Braunschweig, Germany) and having one of the following designations and accession numbers: 1. 58—4B-2, accesssion no. DSM ACC3311, deposited on November 29, 2016; 2. 58—3A, sion no. DSM ACC3312, deposited on November 29, 2016; or 3. 58—1B, accesssion no. DSM ACC3313, ted on November 29, 2016.

The present invention also relates to a peptide sing, preferably consisting of the amino acid sequence of SEQ ID NO: 49, or an immunologically equivalent peptide.

WO 48489 _ 14 _ Preferably said peptide comprises not more than 110, 100, 90, 80, 70, 60, 50, or 40 uous amino acids of CLDN6.

The present invention also s to nucleic acids encoding antibodies or parts thereof, e.g. an antibody chain, or antigen-binding fragments, or peptides as described herein.

Preferably, a nucleic acid of the invention is operatively attached to one or more expression control elements allowing expression in eukaryotic or prokaryotic cells.

Control elements ensuring expression in eukaryotic or prokaryotic cells are well known to those skilled in the art.

A nucleic acid of the invention may be comprised in a vector, e.g., a plasmid, cosmid, virus, bacteriophage or another vector used e.g. conventionally in genetic engineering.

The vector may comprise further genes such as marker genes which allow for the selection ofthe vector in a suitable host cell and under le ions. Furthermore, the vector may comprise expression control elements allowing proper sion of the coding regions in suitable hosts. Such control elements are known to the artisan and may include a promoter, a splice cassette, and a translation tion codon.

Methods for construction of nucleic acid les, for construction of vectors comprising nucleic acid molecules, for introduction of vectors into appropriately chosen host cells, or for causing or achieving expression of nucleic acid molecules are well- known in the art.

A further aspect of the present invention relates to a host cell comprising a nucleic acid or vector as disclosed herein.

A r aspect the present invention relates to the detection of CLDN6 or CLDN6- expressing cells or determination of the quantity of CLDN6 or CLDN6-expressing cells using an antibody or antigen-binding fragment of the invention. CLDN6 or CLDN6— 3O expressing cells are detected or the quantity of CLDN6 or CLDN6—expressing cells is determined by detecting or determining the amount of a complex between CLDN6 and an antibody or n—binding fragment of the invention. Formation of a complex _ 15 - indicates the presence of CLDN6 or CLDN6-expressing cells. Such detection or determination of the amount may be carried out in a number of ways, including but not limited to immunodetection using an antibody or n-binding fragment of the invention. Methods for using antibodies to detect peptides or proteins are well known and include ELISA, competitive binding assays, and the like. In general, such assays use an antibody or antibody fragment that specifically binds the target peptide or n directly or indirectly bound to a label that provides for detection, e.g. indicator enzymes, radiolabels, fluorophores, or paramagnetic les. The methods of the ion allow quantitative and/or ative evaluations, e.g., absolute and/or relative evaluations, of CLDN6 levels or of levels of CLDN6—expressing cells.

In one aspect, the t invention relates to a method for detecting CLDN6 or determining the quantity of CLDN6 in a sample sing the steps of: (i) contacting a sample with an antibody or antigen—binding fragment of the invention or a conjugate of the invention and (ii) detecting the formation of a complex or determining the quantity of a complex between the antibody, the antigen-binding fragment or the conjugate and CLDN6.

In one embodiment, the sample is a cellular sample, Le. a sample sing cells such as cancer cells. In this embodiment, the x is preferably formed between the antibody, the antigen-binding fragment or the conjugate and CLDN6 expressed by cells in said sample.

In one , the present invention relates to a method for determining whether cells express CLDN6 comprising the steps of: (i) contacting a cellular sample with an antibody or antigen—binding fragment ofthe invention or a conjugate of the invention and (ii) detecting the formation of a complex between the antibody, the antigen-binding fragment or the ate and CLDN6 expressed by cells in said sample. _ 16 _ In one embodiment, the cells in the sample are cancer cells. The complex is preferably formed between the antibody, the antigen-binding fragment or the conjugate and CLDN6 expressed by cells in said sample.

Further aspects of the present invention relate to methods of diagnosing or classifying diseases by targeting CLDN6 using an antibody or antigen—binding fragment of the invention. These methods provide for the selective detection of cells that express CLDN6 thereby differentiating these cells from normal cells not expressing CLDN6 or diseased cells not expressing CLDN6. Diseases characterized by diseased cells expressing CLDN6 are treatable by a therapy targeting CLDN6 such as therapy with therapeutic antibodies ed against CLDN6. Preferred diseases for a therapy or sis are those in which CLDN6 is expressed or aberrantly sed, in ular cancer diseases, such as those described . in one aspect the present invention s to methods for diagnosis, detection or monitoring, i.e. determining the regression, progression, course and/or onset, of a cancer disease comprising the detection of CLDN6 or CLDN6—expressing cells and/or determination of the quantity of CLDN6 or CLDN6-expressing cells in a biological sample isolated from a patient using an antibody or antigen-binding fragment of the invention.

Such methods may be used to detect whether a subject has a cancer disease or is at (increased) risk of developing a cancer disease or, for instance, whether a treatment regimen is ent.

Thus, in one , the present ion relates to a method for diagnosis, detection or monitoring of cancer comprising the steps of: (i) contacting a biological sample with an antibody or n—binding fragment of the invention or a conjugate of the invention and (ii) detecting the formation of a complex and/or determining the quantity of a complex between the dy, the antigen—binding fragment or the conjugate and 3O CLDN6. _ 17 _ In one embodiment, the biological sample is a cellular sample, Le. a sample comprising cells such as cancer cells. In this embodiment, the complex is preferably formed between the antibody, the antigen-binding fragment or the conjugate and CLDN6 sed by cells in said sample.

The methods of monitoring according to the invention preferably comprise a detection of and/or determination of the quantity of CLDN6 or CLDN6—expressing cells in a first sample at a first point in time and in a further sample at a second point in time, wherein the regression, progression, course and/or onset of a tumor e may be determined by comparing the two samples.

Typically, the level of CLDN6 or level of CLDN6-expressing cells in a biological sample is compared to a reference level, n a deviation from said reference level is indicative of the presence and/or stage of a cancer disease in a subject. The reference level may be a level as determined in a control sample (e.g., from a healthy tissue or subject, in particular a patient without a cancer disease) or a median level from healthy subjects. A "deviation" from said reference level ates any significant change, such as an increase by at least 10%, 20%, or 30%, preferably by at least 40% or 50%, or even more.

Preferably, the presence of CLDN6 or CLDN6-expressing cells and/or a quantity of CLDN6 or CLDN6—expressing cells which is increased ed to a reference level, e.g. compared to a patient without a cancer disease, indicates the presence of or risk for (Le. a potential for a development of) a cancer disease in the patient.

A quantity of CLDN6 or CLDN6—expressing cells which is decreased compared to a biological sample taken earlier from a patient may indicate a regression, a ve course, e.g. a successful treatment, or a reduced risk for an onset of a cancer disease in a patient.

A quantity of CLDN6 or CLDN6-expressing cells which is increased compared to a biological sample taken r from a t may te a progression, a negative .. 18 ._ , e.g. an unsuccessful treatment, recurrence or metastatic behavior, an onset or a risk for an onset of a cancer disease in said patient. in one , the t invention relates to a method for ining whether a cancer is ble by a cancer therapy ing CLDN6 comprising the steps of: (i) contacting a sample comprising cancer cells with an antibody or antigen-binding fragment ofthe ion or a conjugate of the invention and (ii) detecting the formation of a complex between the antibody, the antigen—binding fragment or the conjugate and CLDN6.

The x is ably formed between the antibody, the antigen-binding fragment or the conjugate and CLDN6 expressed by cancer cells in said sample.

Such methods may be used to detect whether a patient is suitable for a therapy involving the targeting of cells expressing CLDN6 such as a therapy using antibodies exerting one or more immune effector functions such as cytotoxic CLDN6 specific antibodies, e.g. antibodies labeled with a cytotoxic nce such as a toxin or a radiolabel or inducing a cell killing mechanism such as CDC or ADCC. Diseases characterized by diseased cells expressing CLDN6 are treatable by a therapy targeting CLDN6 such as cancer diseases, in particular those described herein.

In one embodiment of any ofthe above aspects, the sample, cellular sample or biological sample is from a patient having a cancer disease, being suspected of having or falling ill with a cancer disease or having a potential for a cancer disease. In one embodiment, the , cellular sample or biological sample is from a tissue or organ wherein the cells when the tissue or organ is free of cancer do not substantially express CLDN6. Preferably said tissue is a tissue other than placenta tissue. Preferably, said tissue has already been diagnosed as being affected by a cancer disease, e.g. by visual inspection or culture testing of cells of said tissue or organ. In this embodiment, the presence of CLDN6 or CLDN6—expressing cells and/or a quantity of CLDN6 or CLDN6—expressing cells which is sed compared to a reference level, e.g. compared to a patient without a tumor _ 19 _ disease, may te that a patient is suitable for a therapy involving the targeting of cells expressing CLDN6. in one aspect, the invention provides compositions, e.g., stic compositions, or kits, comprising an antibody or antigen-binding fragment or a combination of antibodies and/or or antigen-binding nts described herein. Such diagnostic compositions or test kits are useful in the methods of the invention such as the methods for diagnosis, detection or monitoring of the invention. These kits may optionally comprise a detectable label, e.g. indicator enzymes, radiolabels, phores, or paramagnetic particles. Kits may include informative pamphlets, for example, ets informing on how to use ts to practice a method disclosed herein.

Other features and advantages of the instant invention will be apparent from the following detailed description and claims.

Detailed description of the invention Although the present ion is described in detail below, it is to be understood that this invention is not limited to the particular methodologies, ols and reagents described herein as these may vary. It is also to be understood that the terminology used herein is for the e of describing particular embodiments only, and is not intended to limit the scope of the present invention which will be limited only by the appended claims. Unless defined otherwise, all technical and scientific terms used herein have the same meanings as commonly understood by one of ordinary skill in the art. in the following, the elements of the present invention will be described. These elements are listed with specific embodiments, however, it should be tood that they may be combined in any manner and in any number to create additional embodiments. The variously described examples and preferred embodiments should not be construed to limit the present ion to only the explicitly described ments. This description should be understood to support and encompass embodiments which combine the explicitly described embodiments with any number of _ 20 _ the disclosed and/or preferred elements. Furthermore, any ations and combinations of all described ts in this application should be considered disclosed by the description of the present application unless the context indicates otherwise.

Preferably, the terms used herein are d as described in "A multilingual glossary of biotechnological terms: (IUPAC Recommendations)", H.G.W. Leuenberger, B. Nagel, and H. Kélbl, Eds., Helvetica Chimica Acta, CH—4010 Basel, Switzerland, .

The practice of the present invention will employ, unless otherwise ted, conventional methods of chemistry, biochemistry, cell biology, immunology, and recombinant DNA techniques which are explained in the literature in the field (cf., e.g., Molecular Cloning: A Laboratory , 2nd Edition, J. Sambrook et al. eds., Cold Spring Harbor Laboratory Press, Cold Spring Harbor 1989).

Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and ising", will be understood to imply the inclusion of a stated member, integer or step or group of members, integers or steps but not the exclusion of any other member, integer or step or group of members, rs or steps although in some embodiments such other member, r or step or group of members, integers or steps may be excluded, i.e. the subject—matter consists in the inclusion of a stated member, integer or step or group of s, integers or steps. The terms "a" and "an" and "the" and similar reference used in the context of describing the invention (especially in the context of the claims) are to be ued to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. Recitation of ranges of values herein is merely intended to serve as a shorthand method of referring individually to each separate value g within the range. Unless otherwise indicated herein, each individual value is incorporated into the specification as if it were individually recited herein. All s 3O described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context. The use of any and all examples, or exemplary language (e.g., "such as"), provided herein is intended merely to better WO 48489 _ 21 _ illustrate the invention and does not pose a tion on the scope of the invention otherwise claimed. No language in the specification should be construed as indicating any aimed element essential to the practice ofthe invention.

Several documents are cited throughout the text of this specification. Each of the documents cited herein (including all patents, patent applications, scientific publications, manufacturer‘s specifications, instructions, etc.), whether supra or infra, are hereby incorporated by reference in their entirety. Nothing herein is to be construed as an admission that the invention is not ed to antedate such disclosure by virtue of prior ion.

The term "recombinant" in the context of the present invention means "made through genetic engineering". Preferably, a "recombinant object" such as a recombinant cell in the context of the present invention is not occurring naturally.

The term ally occurring" as used herein refers to the fact that an object can be found in nature. For example, a peptide or nucleic acid that is present in an organism (including viruses) and can be isolated from a source in nature and which has not been intentionally ed by man in the laboratory is naturally occurring.

The term "antigen" relates to an agent comprising an epitope against which an immune response is directed and/or is to be generated. Preferably, an antigen in the context of the present invention is a molecule which, optionally after processing, induces an immune reaction, which is preferably specific for the antigen. The term "antigen" includes in particular ns, peptides, ccharides, nucleic acids, especially RNA and DNA, and nucleotides.

The term "epitope" refers to an antigenic inant in a molecule such as an antigen, i.e., to the part in a molecule that is recognized by the immune system, for example, that is recognized by an antibody. For example, epitopes are the discrete, three—dimensional sites on an n, which are recognized by the immune system. Epitopes usually consist of chemically active e groupings of molecules such as amino acids or sugar _ 22 - side chains and usually have specific three ional structural characteristics, as well as specific charge characteristics. Conformational and non—conformational epitopes are distinguished in that the binding to the former but not the latter is lost in the presence of denaturing solvents. An epitope of a protein such as a CLDN ably ses a continuous or discontinuous portion of said protein and is preferably between 5 and 100, preferably n 5 and 50, more preferably between 8 and 30, most preferably between 10 and 25 amino acids in length, for example, the epitope may be preferably 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, or 25 amino acids in .

The term "discontinuous epitope" as used herein, means a mational epitope on a protein antigen which is formed from at least two separate regions in the primary sequence of the protein.

Antigens include tumor—associated antigens, such as CLDN6, i.e., constituents of cancer cells which may be derived from the cytoplasm, the cell surface and the cell nucleus, in particular those antigens which are produced, preferably in large quantity, intracellularly or as surface antigens on cancer cells.

In the context ofthe present invention, the terms "tumor-associated antigen" or "tumor antigen" relate to proteins that are under normal conditions specifically expressed in a limited number of tissues and/or organs or in specific pmental stages, for example, the tumor-associated antigen may be under normal conditions specifically expressed in stomach tissue, preferably in the c mucosa, in reproductive organs, e.g., in testis, in trophoblastic tissue, e.g., in placenta, or in germ line cells, and are expressed or aberrantly sed in one or more tumor or cancer tissues. In this t, "a limited number" preferably means not more than 3, more preferably not more than 2. The tumor-associated antigens in the context of the present invention include, for example, differentiation antigens, preferably cell type specific differentiation antigens, i.e., proteins that are under normal ions specifically expressed in a certain cell type at a certain entiation stage, /testis antigens, i.e., proteins that are under normal conditions specifically expressed in testis and sometimes in placenta, and germ line specific antigens. In the t of the present _ 23 _ invention, the tumor-associated antigen is preferably associated with the cell surface of a cancer cell and is preferably not or only rarely expressed in normal tissues. Preferably, the tumor-associated antigen or the aberrant expression of the tumor-associated antigen identifies cancer cells. In the context of the present invention, the tumor- associated antigen that is expressed by a cancer cell in a subject, e.g., a t suffering from a cancer disease, is ably a self—protein in said subject. In preferred embodiments, the tumor—associated antigen in the context of the present invention is expressed under normal conditions specifically in a tissue or organ that is non-essential, i.e., tissues or organs which when damaged by the immune system do not lead to death of the subject, or in organs or structures of the body which are not or only hardly accessible by the immune system. Preferably, the amino acid sequence of the tumor- associated antigen is identical between the associated antigen which is expressed in normal tissues and the tumor-associated antigen which is expressed in cancer tissues.

Examples for differentiation antigens which ideally fulfill the criteria for tumor- associated antigens as target structures in tumor immunotherapy, in particular, in tumor vaccination are the cell surface proteins of the claudin family, such as CLDN6. Claudins are a family of proteins that are the most important components of tight junctions, where they establish the paracellular barrier that controls the flow of molecules in the ellular space between cells of an epithelium. Claudins are embrane proteins ng the membrane 4 times with the N-terminal and the C—terminal end both located in the cytoplasm.

The term "claudin 6" or "CLDN6" preferably relates to human CLDN6, and, in particular, to a protein comprising the amino acid sequence ing to SEQ ID NO: 1 of the ce g or a variant of said amino acid sequence. In t of CLDN6, the term "variant" in particular refers to a protein comprising the amino acid sequence according to SEQ ID NO: 1 ofthe ce listing wherein the lie at position 143 is replaced by Val.

The term "CLDN6" es any CLDN6 variants such as posttranslationally modified variants and mation variants. c 24 - The term "CLDN9" preferably relates to human CLDN9, and, in particular, to a protein sing the amino acid sequence according to SEQ ID NO: 2 of the sequence listing or a variant of said amino acid sequence.

The term "CLDN4" preferably relates to human CLDN4, and, in particular, to a protein comprising the amino acid sequence according'to SEQ ID N014 of the ce listing or a variant of said amino acid sequence.

The term "CLDN3" preferably s to human CLDN3, and, in particular, to a n comprising the amino acid sequence according to SEQ ID NO: 3 of the sequence g or a variant of said amino acid sequence.

CLDN6 has been found to be sed, for example, in n cancer, lung cancer, gastric cancer, breast cancer, hepatic cancer, pancreatic cancer, skin cancer, melanomas, head neck cancer, sarcomas, bile duct cancer, renal cell cancer, and urinary bladder cancer. CLDN6 is detectable and can be targeted in ovarian cancer, in ular ovarian adenocarcinoma and ovarian teratocarcinoma, lung cancer, including small cell lung cancer (SCLC) and non—small cell lung cancer (NSCLC), in particular squamous cell lung carcinoma and adenocarcinoma, gastric cancer, breast cancer, hepatic cancer, pancreatic cancer, skin cancer, in particular basal cell oma and squamous cell carcinoma, ant melanoma, head and neck cancer, in particular ant rphic adenoma, sarcoma, in particular synovial sarcoma and carcinosarcoma, bile duct cancer, cancer of the urinary bladder, in particular transitional cell carcinoma and papillary carcinoma, kidney cancer, in particular renal cell carcinoma including clear cell renal cell carcinoma and papillary renal cell carcinoma, colon cancer, small bowel cancer, including cancer of the ileum, in particular small bowel adenocarcinoma and adenocarcinoma of the ileum, testicular embryonal oma, placental choriocarcinoma, cervical cancer, testicular , in particular testicular seminoma, testicular teratoma and embryonic testicular cancer, uterine cancer, germ cell tumors such as a teratocarcinoma or an embryonal oma, in particular germ cell tumors of the testis, and the metastatic forms thereof. In one embodiment, the cancer disease associated with CLDN6 expression is selected from the group consisting of ovarian _ 25 _ cancer, lung cancer, metastatic ovarian cancer and metastatic lung cancer. Preferably, the ovarian cancer is a oma or an adenocarcinoma. Preferably, the lung cancer is a carcinoma or an arcinoma, and preferably is bronchiolar cancer such as a bronchiolar carcinoma or bronchiolar adenocarcinoma.

According to the invention, a cell expressing CLDN6 is preferably terized by cell- surface membrane—bound CLDN6, i.e. CLDN6 is associated with the cell surface.

Furthermore, according to the ion, cellular CLDN6 is preferably cell—surface membrane-bound CLDN6. A cell expressing CLDN6 or a cell characterized by association of CLDN6 with its cell surface preferably is a cancer cell, preferably a cancer cell from a cancer described herein.

The term "associated with the cell surface" means that a tumor-associated antigen such as CLDN6 is associated with and located at the plasma membrane of a cell, wherein at least a part ofthe tumor—associated antigen faces the ellular space of said cell and is accessible from the outside of said cell, e.g., by antibodies located outside the cell. In this context, a part is preferably at least 4, preferably at least 8, preferably at least 12, more preferably at least 20 amino acids. The association may be direct or indirect. For example, the association may be by one or more transmembrane domains, one or more lipid anchors, or by the interaction with any other protein, lipid, saccharide, or other structure that can be found on the outer leaflet of the plasma ne of a cell. For example, a tumor—associated antigen associated with the e of a cell may be a transmembrane protein having an extracellular portion or may be a protein associated with the surface of a cell by interacting with another protein that is a transmembrane protein.

"Cell surface" or "surface of a cell" is used in accordance with its normal meaning in the art, and thus includes the outside of the cell which is accessible to g by proteins and other molecules. ing to the invention, CLDN6 is not substantially sed in a cell if the level of expression is lower compared to expression in placenta cells or placenta tissue.

WO 48489 _ 26 ._ Preferably, the level of expression is less than 10%, preferably less than 5%, 3%, 2%, 1%, 0.5%, 0.1% or 0.05% of the expression in placenta cells or placenta tissue or even lower.

Preferably, CLDN6 is not ntially expressed in a cell if the level of sion exceeds the level of expression in non-cancerous tissue other than placenta by no more than 2-fold, preferably 1.5—fold, and ably does not exceed the level of expression in said non—cancerous tissue. Preferably, CLDN6 is not substantially sed in a cell if the level of expression is below the ion limit and/or if the level of expression is too low to allow binding by CLDN6—specific antibodies added to the cells.

According to the invention, CLDN6 is expressed in a cell if the level of expression exceeds the level of expression in non-cancerous tissue other than placenta ably by more than 2-fold, preferably 10—fold, 100-fold, old, or 10000—f0ld. Preferably, CLDN6 is sed in a cell if the level of expression is above the detection limit and/or if the level of expression is high enough to allow binding by CLDN6-specific antibodies added to the cells. Preferably, CLDN6 expressed in a cell is expressed or exposed on the surface of said cell.

The term "antibody" refers to a glycoprotein comprising at least two heavy (H) chains and two light (L) chains inter-connected by disulfide bonds, and es any molecule comprising an antigen binding portion thereof. The term "antibody" includes monoclonal antibodies and fragments or derivatives of antibodies, including, t limitation, human antibodies, humanized antibodies, chimeric antibodies, single chain antibodies, e.g., scFv's and antigen—binding antibody fragments such as Fab and Fab' fragments and also includes all recombinant forms of antibodies, e.g., antibodies expressed in prokaryotes, unglycosylated antibodies, and any antigen-binding antibody fragments and derivatives as described herein. Each heavy chain is comprised of a heavy chain variable region (abbreviated herein as VH) and a heavy chain constant region. Each light chain is comprised of a light chain variable region (abbreviated herein as VL) and a light chain constant region. The VH and VL regions can be further subdivided into regions 3O of hypervariability, termed complementarity determining regions (CDR), interspersed with s that are more conserved, termed framework regions (FR). Each VH and VL is ed of three CDRs and four FRs, arranged from amino—terminus to carboxy- WO 48489 _ 27 _ terminus in the following order: FR1, CDR1, FR2, CDR2, FR3, CDR3, FR4. The variable s of the heavy and light chains contain a binding domain that interacts with an antigen. The constant regions of the antibodies may mediate the binding of the immunoglobulin to host tissues or factors, including various cells of the immune system (e.g., effector cells) and the first component (Clq) of the classical complement system.

The dies described herein may be human antibodies. The term "human antibody", as used herein, is intended to e dies having variable and constant regions derived from human germline immunoglobulin sequences. The human antibodies ofthe invention may include amino acid residues not encoded by human germline immunoglobulin sequences (e.g., mutations introduced by random or site-specific mutagenesis in vitro or by somatic on in viva).

The term "humanized antibody" refers to a molecule having an antigen binding site that is substantially derived from an immunoglobulin from a non—human species, wherein the remaining immunoglobulin structure of the molecule is based upon the ure and/or sequence of a human immunoglobulin. The antigen binding site may either comprise te variable domains fused onto constant domains or only the complementarity determining s (CDR) grafted onto appropriate framework regions in the variable domains. Antigen binding sites may be wild-type or ed by one or more amino acid substitutions, e.g. modified to resemble human immunoglobulins more closely. Some forms of humanized dies preserve all CDR sequences (for example a humanized mouse antibody which contains all six CDRs from the mouse antibody). Other forms have one or more CDRs which are altered with respect to the original antibody.

The term "chimeric dy" refers to those antibodies wherein one portion of each of the amino acid sequences of heavy and light chains is homologous to corresponding sequences in antibodies derived from a particular species or ing to a particular 3O class, while the remaining segment of the chain is homologous to corresponding sequences in another. Typically, the variable region of both light and heavy chains mimics the variable regions of antibodies derived from one s of mammals, while _ 28 _ the constant portions are homologous to sequences of antibodies derived from another.

One clear advantage to such chimeric forms is that the variable region can conveniently be derived from presently known sources using readily available B—cells or hybridomas from non—human host organisms in combination with constant regions derived from, for example, human cell preparations. While the variable region has the advantage of ease of preparation and the specificity is not affected by the source, the nt region being human, is less likely to elicit an immune response from a human subject when the antibodies are injected than would the constant region from a non human source. r the definition is not limited to this particular e.

The terms "antigen—binding portion" of an antibody (or simply "binding portion") or "antigen-binding fragment" of an antibody (or simply "binding fragment") refer to one or more fragments of an dy that retain the ability to specifically bind to an antigen.

It has been shown that the antigen-binding on of an antibody can be performed by fragments of a full—length antibody. Examples of binding fragments encompassed within the term "antigen-binding portion" of an antibody include (i) Fab fragments, monovalent fragments consisting of the VL, VH, CL and CH domains; (ii) F(ab')2 fragments, bivalent fragments sing two Fab fragments linked by a ide bridge at the hinge region; (iii) Fd fragments consisting of the VH and CH domains; (iv) Fv fragments ting of the VL and VH domains of a single arm of an antibody, (v) dAb fragments (Ward et al., (1989) Nature 341: 544-546), which consist of a VH domain; (vi) isolated complementarity determining regions (CDR), and (vii) combinations of two or more isolated CDRs which may optionally be joined by a synthetic linker. Furthermore, although the two domains of the Fv fragment, VL and VH, are coded for by separate genes, they can bejoined, using recombinant methods, by a synthetic linker that s them to be made as a single protein chain in which the VL and VH regions pair to form monovalent molecules (known as single chain Fv (scFv); see e.g., Bird et al. (1988) Science 242: 423-426; and Huston et al. (1988) Proc. Natl. Acad. Sci. USA 85: 883).

Such single chain antibodies are also intended to be encompassed within the term "antigen-binding fragment" of an antibody. A r example is binding-domain immunoglobulin fusion proteins comprising (i) a binding domain polypeptide that is fused to an immunoglobulin hinge region polypeptide, (ii) an immunoglobulin heavy _. 29 _ chain CH2 nt region fused to the hinge , and (iii) an immunoglobulin heavy chain CH3 constant region fused to the CH2 constant region. The g domain polypeptide can be a heavy chain variable region or a light chain variable region. The binding—domain immunoglobulin fusion proteins are further disclosed in US 2003/0118592 and US 2003/0133939. These antibody fragments are obtained using conventional techniques known to those with skill in the art, and the fragments are screened for utility in the same manner as are intact antibodies.

The antibodies described herein may be monoclonal antibodies. The term "monoclonal antibody" as used herein refers to a preparation of antibody molecules of single molecular composition. A monoclonal antibody displays a single binding icity and affinity. In one embodiment, the onal dies are produced by a hybridoma which includes a B cell obtained from a non-human animal, e.g., mouse, fused to an immortalized cell.

The antibodies described herein may be recombinant antibodies. The term "recombinant antibody", as used herein, includes all antibodies that are prepared, expressed, created or isolated by recombinant means, such as (a) antibodies isolated from an animal (e.g., a mouse) that is transgenic or transchromosomal with respect to the immunoglobulin genes or a hybridoma prepared therefrom, (b) antibodies isolated from a host cell transformed to express the dy, e.g., from a transfectoma, (c) antibodies isolated from a recombinant, combinatorial dy y, and (d) antibodies prepared, expressed, created or isolated by any other means that involve splicing of immunoglobulin gene sequences to other DNA sequences.

The term fectoma", as used herein, includes recombinant eukaryotic host cells sing an antibody, such as CHO cells, NS/O cells, HEK293 cells, HEK293T cells, plant cells, or fungi, including yeast cells. 3O As used herein, a "heterologous antibody" is defined in relation to a transgenic organism producing such an antibody. This term refers to an antibody having an amino acid sequence or an encoding c acid sequence corresponding to that found in an W 30 , organism not consisting of the transgenic organism, and being generally derived from a species other than the transgenic organism.

As used herein, a "heterohybrid antibody" refers to an antibody having light and heavy chains of different organismal origins. For example, an dy having a human heavy chain associated with a murine light chain is a heterohybrid antibody.

The invention includes all antibodies and derivatives of antibodies as described herein which for the purposes of the ion are encompassed by the term "antibody". The term "antibody derivatives" refers to any modified form of an antibody, e.g., a conjugate of the antibody and another agent or antibody, or an antibody fragment.

The antibodies described herein are preferably isolated. An "isolated antibody" as used herein, is intended to refer to an dy which is substantially free of other antibodies having ent antigenic specificities. Moreover, an isolated antibody may be substantially free of other cellular material and/or chemicals.

According to the present invention, an dy is capable of binding to a predetermined target if it has a significant affinity for said predetermined target and binds to said predetermined target in standard assays. "Affinity" or "binding affinity" is often measured by equilibrium iation constant (KD). Preferably, the term ficant affinity'l refers to the binding to a predetermined target with a dissociation constant (Kn) of 10‘5 M or lower, 10‘6 M or lower, 10‘7 M or lower, 10‘3M or lower, 10‘9 M or lower, 10' or lower, 10'11 M or lower, or 10'12 M or lower.

An antibody is not (substantially) capable of g to a target if it has no significant ty for said target and does not bind significantly, in particular does not bind detectably, to said target in standard assays. Preferably, the antibody does not detectably bind to said target if present in a concentration of up to 2, preferably 10, more preferably 20, in particular 50 or 100 ug/ml or higher. Preferably, an antibody has no icant affinity for a target if it binds to said target with a KD that is at least 10- fold, 100-fold, 103-fold, 104-fold, IDS—fold, or ld higher than the Km for binding to _ 31 _ the predetermined target to which the antibody is capable of binding. For example, if the KB for binding of an antibody to the target to which the antibody is capable of binding is 10'7 M, the KB for binding to a target for which the antibody has no significant affinity would be is at least 10‘6 M, 10'5 M, 10‘4 M, 10'3 M, 10'2 M, or 10‘1 M.

An antibody is specific for a predetermined target if it is capable of binding to said predetermined target while it is not capable of g to other targets, i.e. has no significant affinity for other targets and does not significantly bind to other targets in standard assays. According to the invention, an antibody is ic for CLDN6 if it is capable of binding to CLDN6 but is not (substantially) capable of binding to other targets, in particular other CLDN proteins such as CLDN9, CLDN4 and/or CLDN3 and/or proteins other than claudin proteins, preferably ns other than CLDN6. Preferably, an antibody is specific for CLDN6 if the affinity for and the binding to such other targets does not significantly exceed the ty for or g to claudin—unrelated proteins such as bovine serum albumin (BSA), casein, human serum albumin (HSA) or non—claudin transmembrane proteins such as MHC molecules or transferrin receptor or any other specified polypeptide. Preferably, an antibody is specific for a predetermined target if it binds to said target with a KD that is at least 10—fold, 100—fold, 103—fold, 104—fold, 105- fold, or 105-fold lower than the KB for binding to a target for which it is not specific. For example, if the K9 for binding of an antibody to the target for which it is specific is 10'7 M, the K9 for binding to a target for which it is not c would be at least 106 M, 10‘ M, 10'4 M, 10‘3 M, 10‘2 M, or 10‘1 M.

Binding of an antibody to a target can be determined experimentally using any suitable method; see, for example, Berzofsky et al., "Antibody-Antigen Interactions" In Fundamental Immunology, Paul, W. E., Ed., Raven Press New York, N Y (1984), Kuby, Janis Immunology, W. H. Freeman and Company New York, N Y (1992), and s described herein. Affinities may be readily ined using conventional techniques, such as by equilibrium dialysis; by using the BlAcore 2000 instrument, using l procedures outlined by the manufacturer; by radioimmunoassay using radiolabeled target antigen; or by r method known to the skilled artisan. The ty data may be analyzed, for example, by the method of Scatchard et al., Ann N.Y. Acad. ScL, 512660 _ 32 - (1949). The measured affinity of a particular antibody-antigen interaction can vary if measured under different conditions, e.g., salt concentration, pH. Thus, measurements of affinity and other antigen-binding parameters, e.g., KD, lcso, are preferably made with standardized ons of antibody and antigen, and a standardized .

The term te" refers to the competition between two antibodies for g to a target antigen. lftwo antibodies do not block each other for binding to a target antigen, such antibodies are non-competing and this is an indication that said antibodies do not bind to the same part, Le. epitope, of the target antigen. It is well known to a person skilled in the art how to test for competition of antibodies for binding to a target antigen.

An example of such a method is a so—called cross—competition assay, which may e.g. be performed as an ELISA or by flow-cytometry. For example an ELISA-based assay may be performed by g ELISA plate wells with one ofthe dies; adding the ing antibody and His-tagged antigen/target and detecting whether the added dy inhibited binding of the His-tagged antigen to the coated antibody, e.g., by adding biotinylated anti-His antibody, followed by Streptavidin—poly-HRP, and r developing the reaction with ABTS and measuring the absorbance at 405 nm. For example a flow-cytometry assay may be performed by incubating cells expressing the n/target with an excess of unlabeled antibody, incubating the cells with a sub- optimal concentration of biotin—labelled antibody, followed by incubation with fluorescently labeled streptavidin and analyzing by flow cytometry.

Two antibodies have the "same specificity" if they bind to the same antigen and to the same epitope. Whether an antibody to be tested recognizes the same epitope as a certain antigen—binding dy, i.e., the antibodies bind to the same epitope, can be tested by different methods known to the skilled person, e.g., based on the competition of the antibodies for the same epitope. The competition between the antibodies can be detected by a cross—blocking assay. For example, a competitive ELISA assay may be used as a cross—blocking assay. For example, target antigen may be coated on the wells of a 3O microtiter plate and antigen-binding dy and ate competing test antibody may be added. The amount of the antigen-binding antibody bound to the antigen in the well indirectly correlates with the binding ability of the ate competing test _ 33 _. dy that competes therewith for binding to the same epitope. ically, the larger the affinity of the candidate ing test antibody is for the same epitope, the smaller the amount of the antigen—binding antibody bound to the antigen-coated well.

The amount of the antigen-binding antibody bound to the well can be measured by labeling the antibody with detectable or able labeling substances.

An antibody competing for binding to an antigen with another antibody, e.g., an dy comprising heavy and light chain variable regions as described herein, or an antibody having the specificity for an antigen of another antibody, e.g., an antibody comprising heavy and light chain le regions as described herein, may be an dy comprising variants of said heavy and/or light chain variable regions as described herein, e.g. modifications in the CDRs and/or a certain degree of identity as described .

As used herein, "isotype" refers to the antibody class (e.g., lgM or lgGl) that is encoded by heavy chain constant region genes. Antibodies according to the invention include polyclonal and monoclonal antibodies and include lgGZa (e.g. IgGZa, K, A), IgGZb (e.g. lgGZb, K, A), lgG3 (e.g. lgGB, K, A) and lgM dies. However, other antibody isotypes are also encompassed by the invention, including IgGl, lgAl, lgA2, secretory IgA, lgD, and IgE antibodies.

As used herein, "isotype switching" refers to the phenomenon by which the class, or isotype, of an antibody changes from one lg class to one of the other lg classes.

The term "rearranged" as used herein refers to a configuration of a heavy chain or light chain immunoglobulin locus wherein a V segment is positioned immediately adjacent to a D—J orJ t in a conformation encoding essentially a complete VH or VL domain, respectively. A rearranged immunoglobulin (antibody) gene locus can be identified by comparison to germline DNA; a rearranged locus will have at least one recombined heptamer/nonamer homology element. _ 34 _ The term rranged" or "germline configuration" as used herein in nce to a V segment refers to the configuration wherein the V segment is not recombined so as to be ately adjacent to a D or] segment.

According to the invention, antibodies may be derived from different species, ing but not d to mouse, rat, rabbit, guinea pig and human. Antibodies also include chimeric molecules in which an antibody constant region derived from one species, preferably human, is combined with the antigen binding site derived from another species. Moreover, dies include humanized molecules in which the antigen binding sites of an antibody derived from a non—human species are ed with constant and framework regions of human origin.

Antibodies can be produced by a variety of techniques, including conventional monoclonal antibody methodology, e.g., the standard somatic cell hybridization technique of Kohler and in, Nature 256: 495 (1975). Although c cell hybridization procedures are preferred, in principle, other techniques for producing monoclonal antibodies can be employed, e.g., viral or oncogenic transformation of B— lymphocytes or phage display ques using libraries of antibody genes. 2O The preferred animal system for preparing hybridomas that secrete monoclonal antibodies is the murine system. Hybridoma production in the mouse is a very well established procedure. Immunization protocols and techniques for isolation of immunized cytes for fusion are known in the art. Fusion partners (e.g., murine myeloma cells) and fusion procedures are also known.

Other preferred animal systems for preparing hybridomas that secrete monoclonal antibodies are the rat and the rabbit system (e.g. described in Spieker—Polet et al., Proc.

Natl. Acad. Sci. U.S.A. 9229348 (1995), see also Rossi et al., Am. J. Clin. Pathol. 124: 295 (2005)).

In yet another preferred embodiment, human monoclonal antibodies directed against CLDN6 can be generated using transgenic or hromosomal mice carrying parts of _ 35 _ the human immune system rather than the mouse system. These transgenic and transchromosomic mice include mice known as HuMAb mice and KM mice, respectively, and are collectively referred to herein as "transgenic mice." The production of human antibodies in such transgenic mice can be performed as bed in detail for CD20 in W02004 035607 Yet another strategy for generating monoclonal antibodies is to directly isolate genes encoding antibodies from cytes producing antibodies of defined specificity; see e.g. k et al., 1996; A novel strategy for generating monoclonal antibodies from single, isolated lymphocytes producing antibodies of d specificities. For details of recombinant antibody engineering see also Welschof and Kraus, Recombinant antibodes for cancer therapy —89603-918—8 and Benny K.C. Lo Antibody Engineering ISBN 1-58829—092-1.

To generate dies to CLDN6, mice can be immunized with r-conjugated peptides derived from the CLDN6 sequence, an enriched preparation of recombinantly expressed CLDN6 antigen or fragments f and/or cells expressing CLDN6 or fragments thereof, as described. Alternatively, mice can be immunized with DNA encoding full length human CLDN6 or fragments thereof. In the event that immunizations using a purified or enriched preparation of the CLDN6 antigen do not result in antibodies, mice can also be immunized with cells expressing CLDN6, e.g., a cell line, to promote immune responses.

The immune response can be monitored over the course of the immunization protocol with plasma and serum samples being obtained by tail vein or retroorbital bleeds. Mice with sufficient titers of anti—CLDN6 immunoglobulin can be used for fusions. Mice can be boosted intraperitonealy or intravenously with CLDN6 expressing cells 3—5 days before sacrifice and removal of the spleen to increase the rate of specific antibody secreting hybridomas.

To generate hybridomas producing monoclonal dies to CLDN6, cells from lymph nodes, spleens or bone marrow obtained from immunized mice can be isolated and - 36 _ fused to an appropriate alized cell line, such as a mouse myeloma cell line. The resulting hybridomas can then be screened for the production of antigen-specific antibodies. Individual wells can then be screened by ELISA for antibody secreting hybridomas. By lmmunofluorescence and FACS analysis using CLDN6 expressing cells, antibodies with specificity for CLDN6 can be identified. The dy secreting hybridomas can be replated, screened again, and if still positive for anti-CLDN6 monoclonal antibodies can be ned by limiting dilution. The stable subclones can then be cultured in vitro to generate antibody in tissue culture medium for characterization.

Antibodies of the invention can also be produced in a host cell transfectoma using, for example, a combination of recombinant DNA techniques and gene transfection s as are well known in the art (Morrison, S. (1985) e 229: 1202).

For example, in one embodiment, the gene(s) of interest, e.g., antibody genes, can be ligated into an expression vector such as a eukaryotic expression plasmid such as used by the GS gene expression system disclosed in WO 62, WO 89/01036 and EP 338 841 or other expression systems well known in the art. The purified plasmid with the cloned antibody genes can be introduced in eukaryotic host cells such as CHO cells, NS/O cells, HEK293T cells or HEK293 cells or alternatively other eukaryotic cells like plant derived cells, fungal or yeast cells. The method used to introduce these genes can be methods described in the art such as electroporation, lipofectine, lipofectamine or others. After introduction of these antibody genes in the host cells, cells expressing the antibody can be identified and selected. These cells represent the ectomas which can then be amplified for their expression level and upscaled to e antibodies.

Recombinant antibodies can be isolated and purified from these culture supernatants and/or cells. atively, the cloned antibody genes can be expressed in other expression systems, including prokaryotic cells, such as microorganisms, e.g. E. coli. Furthermore, the antibodies can be produced in transgenic man animals, such as in milk from sheep and rabbits or in eggs from hens, or in transgenic plants; see e.g. Verma, R., et al.

WO 48489 .. 37 _ (1998) J. Immunol. Meth. 216: 1; Pollock, et al. (1999) J. lmmunol. Meth. 231: 147-157; and Fischer, R., et al. (1999) Biol. Chem. 380: 825-839.

Chimeric antibodies are antibodies, the different portions of which are derived from different animal species, such as those having a variable region derived from a murine dy and a human immunoglobulin constant region. Chimerisation of antibodies is achieved by g of the variable regions ofthe murine antibody heavy and light chain with the constant region of human heavy and light chain (e.g. as described by Kraus et al., in Methods in lar y series, Recombinant antibodies for cancer y ISBN-O-89603—918—8). In a preferred embodiment, chimeric antibodies are generated by joining human kappa-light chain constant region to murine light chain variable region.

In an also preferred embodiment, chimeric antibodies can be generated by joining human lambda—light chain constant region to murine light chain variable region. The preferred heavy chain constant regions for generation of chimeric antibodies are lgGl, IgG3 and lgG4. Other preferred heavy chain constant regions for generation of chimeric antibodies are IgGZ, lgA, IgD and lgM.

Antibodies interact with target antigens predominantly through amino acid residues that are located in the six heavy and light chain complementarity determining regions (CDRs). For this reason, the amino acid sequences within CDRs are more diverse between dual antibodies than ces outside of CDRs. Because CDR ces are responsible for most antibody-antigen ctions, it is possible to express recombinant antibodies that mimic the properties of specific naturally occurring antibodies by constructing expression vectors that include CDR sequences from the specific naturally occurring antibody grafted onto framework sequences from a different antibody with different properties (see, e.g., Riechmann, L. et al. (1998) Nature 332: 323— 327; Jones, P. et al. (1986) Nature 321: 522-525; and Queen, C. et al. (1989) Proc. Natl.

Acad. Sci. U. S. A. 86: 10029-10033). Such framework sequences can be obtained from public DNA databases that include germline antibody gene sequences. These ne 3O sequences will differ from mature dy gene sequences because they will not include completely assembled variable genes, which are formed by V (D) J joining during B cell maturation. Germline gene sequences will also differ from the sequences of a high WO 48489 _ 3g _ affinity secondary repertoire antibody at individual positions evenly across the variable region. For example, somatic mutations are relatively infrequent in the amino terminal portion of framework region 1 and in the y— terminal portion ework region 4. Furthermore, many c mutations do not significantly alter the binding properties of the dy. For this reason, it is not necessary to obtain the entire DNA sequence of a particular antibody in order to recreate an intact recombinant antibody having binding ties similar to those of the original antibody (see WO 62).

Partial heavy and light chain sequences spanning the CDR regions are typically sufficient for this purpose. The partial sequence is used to determine which germline variable and joining gene segments contributed to the recombined antibody variable genes. The ne sequence is then used to fill in missing portions of the variable regions. Heavy and light chain leader sequences are cleaved during n maturation and do not contribute to the properties of the final antibody. To add missing sequences, cloned cDNA sequences can be combined with synthetic oligonucleotides by ligation or PCR amplification. Alternatively, the entire variable region can be synthesized as a set of short, overlapping, oligonucleotides and combined by PCR amplification to create an ly synthetic variable region clone. This process has certain advantages such as elimination or inclusion or particular restriction sites, or optimization of particular codons.

The nucleotide sequences of heavy and light chain transcripts from hybridomas may be used to design an overlapping set of synthetic oligonucleotides to create synthetic V sequences with cal amino acid coding capacities as the natural sequences. The synthetic heavy and kappa chain sequences can differ from the natural sequences in three ways: strings of repeated nucleotide bases are interrupted to facilitate oligonucleotide synthesis and PCR amplification; optimal translation initiation sites are incorporated according to Kozak's rules , 1991, J. Biol. Chem. 266: 19867-19870); and Hindlll sites are engineered am of the translation initiation sites.

For both the heavy and light chain variable regions, the optimized coding and corresponding non-coding, strand sequences are broken down into 30-50 tides approximately at the midpoint of the corresponding ding oligonucleotide. Thus, - 39 _ for each chain, the oligonucleotides can be assembled into overlapping double stranded sets that span segments of 150-400 nucleotides. The pools are then used as templates to produce PCR amplification products of 150-400 nucleotides. lly, a single variable region oligonucleotide set will be broken down into two pools which are separately ied to generate two overlapping PCR products. These overlapping products are then combined by PCR amplification to form the complete variable .

It may also be desirable to include an overlapping nt of the heavy or light chain constant region in the PCR amplification to generate fragments that can easily be cloned into the expression vector constructs.

The reconstructed chimerized or humanized heavy and light chain variable regions are then combined with cloned promoter, leader, translation tion, constant region, 3‘ untranslated, polyadenylation, and transcription termination sequences to form expression vector constructs. The heavy and light chain expression constructs can be combined into a single , nsfected, serially transfected, or separately transfected into host cells which are then fused to form a host cell expressing both chains. Plasmids for use in construction of expression s for human IgGK are described. The plasmids can be constructed so that PCR amplified V heavy and V kappa light chain cDNA ces can be used to reconstruct complete heavy and light chain minigenes. These plasmids can be used to express completely human, or chimeric lgGl, Kappa or lgG4, Kappa antibodies. Similar plasmids can be constructed for expression of other heavy chain isotypes, or for expression of antibodies comprising lambda light chains.

Thus, in another aspect of the invention, the structural features of the anti—CLDN6 antibodies described herein, are used to create structurally related humanized anti- CLDN6 antibodies that retain at least one functional property of the antibodies of the ion, such as binding to CLDNB. More specifically, one or more CDR regions of mouse monoclonal antibodies can be combined recombinantly with known human framework regions and CDRs to create additional, recombinantly-engineered, zed anti—CLDN6 antibodies. _ 40 _ The ability of an antibody to bind CLDN6 can be determined using standard binding assays, e.g., ELISA, Western Blot, Immunofluorescence and Flow cytometric analysis.

ELISA can be used to demonstrate the presence of antibodies in sera of immunized mice or binding of monoclonal antibodies to CLDN6 protein or peptides. es or protein used for immunization may be used for determining the specificity of hybridoma supernatants or analysing serum .

In order to demonstrate presence of antibodies in sera of immunized mice or binding of monoclonal antibodies to living cells, flow cytometry can be used. Cell lines expressing naturally or after transfection antigen and ve controls lacking antigen expression (grown under standard growth conditions) can be mixed with various concentrations of monoclonal antibodies in hybridoma supernatants or in PBS containing 1% FBS, and can be incubated at 4°C for 30 min. After washing, the APC— or Alexa647—labeled anti IgG antibody can bind to antigen-bound onal antibody under the same ions as the y antibody staining. The samples can be analyzed by flow cytometry with a FACS instrument using light and side scatter properties to gate on single, living cells. In order to distinguish antigen—specific monoclonal antibodies from non—specific binders in a single measurement, the method of co-transfection can be employed. Cells transiently transfected with plasmids encoding antigen and a fluorescent marker can be stained as described above. Transfected cells can be detected in a different fluorescence channel than antibody—stained cells. As the majority oftransfected cells express both transgenes, antigen-specific monoclonal dies bind preferentially to fluorescence marker sing cells, whereas ecific antibodies bind in a comparable ratio to non— ected cells. An alternative assay using scence microscopy may be used in on to or instead of the flow cytometry assay. Cells can be stained exactly as described above and examined by scence microscopy.

In order to demonstrate presence of anti-CLDN6 dies in sera of immunized mice or binding of monoclonal antibodies to living cells expressing CLDN6, immunofluorescence microscopy analysis can be used. For example, cell lines expressing either spontaneously or after transfection CLDN6 and negative controls lacking CLDN6 _ 41 _ expression are grown in chamber slides under standard growth conditions in 12 medium, supplemented with 10 % fetal calf serum (FCS), 2 mM L-glutamine, 100 IU/ml penicillin and ICC ug/ml streptomycin. Cells can then be fixed with methanol or paraformaldehyde or left untreated. Cells can then be reacted with monoclonal antibodies against CLDN6 for 30 min. at 25°C. After washing, cells can be reacted with an Alexa555—labelled anti-mouse IgG secondary antibody (Molecular Probes) under the same conditions. Cells can then be examined by fluorescence microscopy.

Total CLDN6 levels in cells can be observed when cells are methanol fixed or paraformaldehyde fixed and permeabilized with Triton X-100. in living cells and non- permeabilized, paraformaldehyde fixed cells surface localization of CLDN6 can be examined. Additionally targeting of CLDN6 to tight ons can be analyzed by co- staining with tight junction markers such as 20—1. Furthermore, s of antibody binding and CLDN6 localization within the cell membrane can be examined.

Anti—CLDN6 IgG can be further tested for reactivity with CLDN6 antigen by Western Blotting. Briefly, cell extracts from cells sing CLDN6 and appropriate negative controls can be prepared and subjected to sodium dodecyl sulfate (SDS) polyacrylamide gel electrophoresis. After ophoresis, the separated antigens will be transferred to 2O nitrocellulose membranes, blocked, and probed with the monoclonal antibodies to be tested. lgG g can be detected using anti-mouse lgG peroxidase and developed with ECL substrate.

Anti—CLDN6 mouse lgGs can be further tested for reactivity with CLDN6 antigen by lmmunohistochemistry in a manner well known to the skilled person, e.g. using paraformaldehyde or e fixed cryosections or paraffin embedded tissue sections fixed with rmaldehyde from non—cancer tissue or cancer tissue s obtained from patients during routine surgical procedures or from mice carrying xenografted tumors ated with cell lines expressing spontaneously or after transfection with 3O CLDN6. For immunostaining, antibodies reactive to CLDN6 can be incubated followed by adish-peroxidase conjugated goat anti—mouse or goat anti-rabbit antibodies according to the vendors instructions.

WO 48489 2018/073883 One particularly preferred methodology for assaying CLDN6 in the s of the ion is lmmunohistochemistry or IHC. lmmunohistochemistry or IHC refers to the process of detecting antigens (e.g., proteins) in cells of a tissue section, e.g. cells of the tissues mentioned herein. lmmunohistochemical staining is widely used in the diagnosis of abnormal cells such as those found in cancerous tumors. Visualising an antibody— antigen ction can be accomplished in a number of ways. In the most common instance, an antibody is conjugated to an enzyme, such as peroxidase, that can catalyse a colour-producing reaction. Alternatively, the antibody can also be tagged to a phore, such as fluorescein or rhodamine.

Preparation ofthe sample is critical to maintain cell morphology, tissue architecture and the antigenicity of target epitopes. This requires proper tissue collection, on and ning. Paraformaldehyde is usually used with fixation. Depending on the purpose and the thickness of the experimental sample, either thin (about 4—40 pm) sections are sliced from the tissue of interest, or if the tissue is not very thick and is penetrable it is used whole. The slicing is usually lished through the use of a microtome, and slices are mounted on slides. 2O The sample may require additional steps to make the epitopes available for antibody binding, including deparaffinization and antigen retrieval. Detergents like Triton X-100 are generally used in lmmunohistochemistry to reduce surface tension, ng less reagent to be used to achieve better and more even coverage of the sample.

The direct method of immunohistochemical staining uses one labelled antibody, which binds directly to the antigen being stained for. The indirect method of histochemical ng which is more common uses one antibody against the antigen being probed for, and a second, labelled, antibody against the first. 3O To reduce background staining in IHC, the samples are incubated with a buffer that blocks the reactive sites to which the primary or secondary antibodies may otherwise bind. Primary antibodies are raised against an antigen of interest and are typically _ 43 _ unconjugated (unlabelled), while secondary antibodies are raised against immunoglobulins of the primary antibody species. The secondary antibody is usually conjugated to a linker molecule, such as biotin, that then recruits reporter molecules, or the ary antibody is directly bound to the er molecule itself. Common blocking buffers include normal serum, non—fat dry milk, BSA or gelatin, and commercial blocking buffers. er molecules vary based on the nature of the ion method, and the most popular methods of detection are with enzyme- and fluorophore-mediated chromogenic and fluorescence ion, respectively. With chromogenic reporters, an enzyme label is reacted with a substrate to yield an intensely colored t that can be analyzed with an ordinary light microscope. While the list of enzyme substrates is extensive, alkaline atase (AP) and horseradish peroxidase (HRP) are the two enzymes used most extensively as labels for protein detection. An array of chromogenic, fluorogenic and chemiluminescent substrates is available for use with either enzyme, including DAB or BClP/NBT. Fluorescent reporters are small, organic molecules used for IHC detection. For chromogenic and fluorescent ion methods, densitometric analysis of the signal can provide semi- and fully—quantitative data, respectively, to correlate the level of reporter signal to the level of protein expression or localization.

After immunohistochemical staining ofthe target antigen, 3 second stain is often applied to provide contrast that helps the primary stain stand out. Many of these stains show specificity for discrete cellular compartments or antigens, while others will stain the whole cell. Both genic and scent dyes are available for lHC to provide a vast array of reagents to fit every experimental design. xylin, Hoechst stain and DAPl are commonly used.

Mapping of epitopes recognized by antibodies can be performed as described in detail in "Epitope Mapping Protocols (Methods in Molecular Biology) by Glenn E. Morris ISBN— 3O 089603—375—9 and in "Epitope Mapping: A Practical Approach" Practical Approach Series, 248 by Olwyn M. R. Westwood, Frank C. Hay. _ 44 _ The term "immune effector ons" in the context of the present invention includes any functions mediated by components of the immune system that result in the inhibition oftumor growth and/or tion oftumor development, including inhibition of tumor dissemination and asis. Preferably, immune effector functions result in killing of cancer cells. Preferably, the immune effector functions in the context of the present invention are antibody—mediated effector functions. Such functions comprise complement ent cytotoxicity (CDC), antibody-dependent cell-mediated xicity (ADCC), antibody—dependent cell-mediated phagocytosis (ADCP), induction of apoptosis in the cells carrying the tumor-associated n, for example, by binding of the antibody to a surface antigen, inhibition of CD40L—mediated signal uction, for example, by binding of the antibody to the CD40 receptor or CD40 ligand (CD4OL), and/or inhibition of proliferation of the cells carrying the tumor—associated antigen, preferably ADCC and/or CDC. Thus, antibodies that are capable of mediating one or more immune effector functions are preferably able to mediate killing of cells by inducing CDC—mediated lysis, ADCC-mediated lysis, apoptosis, homotypic on, and/or phagocytosis, preferably by inducing CDC-mediated lysis and/or ADCC-mediated lysis. dies may also exert an effect simply by binding to tumor—associated antigens on the surface of a cancer cell. For example, antibodies may block the on of the tumor—associated antigen or induce apoptosis just by binding to the tumor—associated antigen on the e of a cancer cell.

ADCC describes the cell-killing ability of effector cells, in particular lymphocytes, which preferably requires the target cell being marked by an antibody. ADCC preferably occurs when antibodies bind to antigens on cancer cells and the dy Fc domains engage Fc receptors (FcR) on the surface of immune or cells. Several families of Fc receptors have been identified, and ic cell populations characteristically express d Fc receptors. ADCC can be viewed as a mechanism to directly induce a variable degree of immediate tumor destruction that also leads to antigen presentation and the induction of tumor—directed T—cell responses. Preferably, in vivo induction of ADCC will lead to tumor—directed T—cell responses and further host-derived antibody responses. _ 45 _ CDC is another cell—killing method that can be directed by antibodies. lgM is the most effective isotype for complement activation. lgGl and lgG3 are also both very effective at directing CDC via the classical complement-activation pathway. Preferably, in this cascade, the formation of antigen—antibody complexes results in the uncloaking of multiple Clq binding sites in close proximity on the CH2 domains of participating dy molecules such as lgG molecules (Clq is one of three subcomponents of complement C1). Preferably these uncloaked C1q binding sites convert the previously finity G interaction to one of high avidity, which triggers a cascade of events involving a series of other complement proteins and leads to the proteolytic release of the effector-cell chemotactic/activating agents C3a and C5a. ably, the complement cascade ends in the formation of a membrane attack complex, which creates pores in the cell membrane that facilitate free passage of water and solutes into and out of the cell and may lead to apoptosis.

The term "immune effector cells" in the context ofthe present invention relates to cells which exert effector functions during an immune reaction. For e, such cells secrete nes and/or chemokines, kill microbes, secrete antibodies, recognize cancerous cells, and optionally eliminate such cells. For e, immune effector cells comprise T-cells (cytotoxic T—cells, helper T-cells, tumor infiltrating T—cells), B—cells, natural killer cells, neutrophils, hages, and tic cells.

A c acid is according to the invention preferably deoxyribonucleic acid (DNA) or ribonucleic acid (RNA), more preferably RNA, most preferably in vitro transcribed RNA (IVT RNA). Nucleic acids include ing to the invention genomic DNA, cDNA, mRNA, recombinantly prepared and chemically synthesized molecules. A nucleic acid may according to the invention be in the form of a molecule which is single stranded or double stranded and linear or closed covalently to form a circle. A nucleic can be employed for introduction into, i.e. transfection of, cells, for example, in the form of RNA which can be prepared by in vitro transcription from a DNA template. The RNA can 3O moreover be modified before ation by stabilizing sequences, capping, and polyadenylation. - 46 , The c acids described herein may be sed in a vector. The term "vector" as used herein includes any vectors known to the skilled person including plasmid vectors, cosmid s, phage vectors such as lambda phage, viral vectors such as iral or baculoviral vectors, or artificial chromosome vectors such as bacterial artificial chromosomes (BAC), yeast artificial chromosomes (YAC), or P1 artificial chromosomes (PAC). Said vectors include sion as well as cloning vectors. sion vectors comprise plasmids as well as viral vectors and generally contain a desired coding sequence and appropriate DNA sequences necessary for the expression of the operably linked coding sequence in a particular host organism (e.g., bacteria, yeast, plant, insect, or mammal) or in in vitro expression s. Cloning vectors are generally used to engineer and amplify a certain desired DNA fragment and may lack functional sequences needed for expression of the desired DNA fragments.

As the vector for expression of an antibody, either of a vector type in which the antibody chains are present in ent vectors or a vector type in which the antibody chains are present in the same vector can be used.

As used herein, the term "RNA" means a molecule comprising ribonucleotide residues.

By "ribonucleotide" is meant a nucleotide with a hydroxyl group at the 2'-position of a 2O beta—D—ribo—furanose . The term includes double stranded RNA, single stranded RNA, isolated RNA such as partially purified RNA, essentially pure RNA, synthetic RNA, recombinantly produced RNA, as well as d RNA that s from naturally occurring RNA by the addition, deletion, substitution and/or alteration of one or more nucleotides. Such alterations can include addition of non-nucleotide material, such as to the end(s) of a RNA or internally, for example at one or more tides of the RNA.

Nucleotides in RNA molecules can also comprise non-standard nucleotides, such as non— naturally occurring nucleotides or chemically synthesized nucleotides or deoxynucleotides. These altered RNAs can be referred to as analogs or analogs of naturally-occurring RNA.

According to the t invention, the term "RNA" includes and preferably relates to "mRNA" which means "messenger RNA" and relates to a "transcript" which may be _ 47 _ produced using DNA as template and encodes a peptide or protein. mRNA typically comprises a 5’ non translated , a protein or e coding region and a 3’ non ated region. mRNA has a limited halftime in cells and in vitro.

In the context of the present invention, the term "transcription" relates to a process, wherein the genetic code in a DNA sequence is transcribed into RNA.

The nucleic acids described according to the invention have preferably been isolated.

The term "isolated nucleic acid" means according to the invention that the nucleic acid was (i) amplified in vitro, for example by polymerase chain reaction (PCR), (ii) inantly produced by cloning, (iii) purified, for example by cleavage and gel- electrophoretic fractionation, or (iv) synthesized, for example by chemical synthesis. An isolated nucleic acid is a nucleic acid which is ble for lation by recombinant DNA techniques.

Nucleic acids may, according to the invention, be present alone or in ation with other nucleic acids, which may be homologous or heterologous. In preferred embodiments, a nucleic acid is functionally linked to expression control sequences which may be homologous or heterologous with t to said nucleic acid. The term "homologous" means that the nucleic acids are also functionally linked naturally and the term "heterologous" means that the nucleic acids are not functionally linked naturally.

A nucleic acid and an expression control sequence are "functionally" linked to one another, if they are covalently linked to one another in such a way that expression or transcription of said nucleic acid is under the control or under the influence of said sion control sequence. If the nucleic acid is to be translated into a functional protein, then, with an expression l sequence functionally linked to a coding sequence, induction of said expression l sequence results in transcription of said nucleic acid, without causing a frame shift in the coding sequence or said coding 3O sequence not being capable of being translated into the d protein or peptide.

The term "expression control sequence" or ssion control element" comprises WO 48489 _ 43 - according to the invention promoters, ribosome binding sites, enhancers and other control elements which regulate transcription of a gene or translation of a mRNA. in ular embodiments of the invention, the expression control sequences can be regulated. The exact structure of expression control sequences may vary as a function of the species or cell type, but generally comprises 5'—untranscribed and 5’- and 3’— untranslated sequences which are involved in initiation of transcription and translation, respectively, such as TATA box, capping sequence, CAAT sequence, and the like. More specifically, 5’-untranscribed expression control sequences comprise a promoter region which includes a er sequence for transcriptional l ofthe onally linked nucleic acid. Expression control sequences may also comprise enhancer ces or upstream activator sequences.

According to the invention the term "promoter" or "promoter region" relates to a nucleic acid sequence which is located upstream (5’) to the nucleic acid sequence being expressed and controls expression of the sequence by providing a ition and binding site for RNA-polymerase. The "promoter region" may include further recognition and binding sites for further s which are involved in the regulation of transcription of a gene. A er may control the transcription of a prokaryotic or eukaryotic gene. Furthermore, a promoter may be "inducible" and may te transcription in response to an inducing agent or may be "constitutive" if ription is not controlled by an inducing agent. A gene which is under the control of an inducible promoter is not expressed or only expressed to a small extent if an inducing agent is absent. In the presence of the inducing agent the gene is switched on or the level of transcription is increased. This is mediated, in general, by binding of a specific transcription factor.

Promoters which are preferred according to the invention include promoters for SP6, T3 and T7 polymerase, human U6 RNA promoter, CMV promoter, and artificial hybrid promoters f (e.g. CMV) where a part or parts are fused to a part or parts of promoters of genes of other cellular proteins such as e.g. human GAPDH (glyceraIdehyde—3—phosphate dehydrogenase), and including or not ing (an) additional intron(s).

The term "expression" is used herein in its broadest meaning and comprises the production of RNA or of RNA and protein or peptide. With respect to RNA, the term "expression" or "translation" relates in particular to the tion of peptides or ns. Expression may be transient or may be stable. According to the invention, the term expression also includes an "aberrant expression" or "abnormal expression".

"Aberrant expression" or "abnormal expression" means according to the invention that sion is altered, preferably increased, compared to a reference, e.g. a state in a subject not having a disease associated with aberrant or abnormal expression of a certain protein, e.g., a tumor-associated n. An se in expression refers to an increase by at least 10%, in particular at least 20%, at least 50% or at least 100%, or more. In one embodiment, expression is only found in a diseased tissue, while expression in a healthy tissue is repressed.

The term "specifically expressed" means that a protein is essentially only expressed in a specific tissue or organ. For example, a associated n specifically sed in gastric mucosa means that said protein is primarily expressed in gastric mucosa and is not expressed in other tissues or is not expressed to a significant extent in other tissue or organ types. Thus, a protein that is ively expressed in cells ofthe gastric mucosa and to a significantly lesser extent in any other tissue is specifically expressed in cells of the gastric mucosa. in some embodiments, a associated antigen may also be specifically expressed under normal conditions in more than one tissue type or organ, such as in 2 or 3 tissue types or organs, but ably in not more than 3 different tissue or organ types. In this case, the tumor—associated antigen is then specifically expressed in these organs.

The term "translation" according to the invention relates to the process in the ribosomes of a cell by which a strand of messenger RNA directs the assembly of a sequence of amino acids to make a protein or peptide.

WO 48489 _ 50 _ According to the invention, the term "nucleic acid encoding" means that nucleic acid, if present in the appropriate environment, ably within a cell, can be expressed to e a n or peptide it encodes.

The term "peptide" comprises oligo- and polypeptides and refers to substances comprising two or more, preferably 3 or more, preferably 4 or more, preferably 6 or more, preferably 8 or more, preferably 9 or more, preferably 10 or more, preferably 13 or more, preferably 16 more, preferably 21 or more and up to preferably 8, 10, 20, 30, 40 or 50, in particular 100 amino acids joined covalently by peptide bonds. The term "protein" refers to large peptides, preferably to peptides with more than 100 amino acid residues, but in general the terms des" and "proteins" are ms and are used interchangeably herein. ably, the proteins and peptides described according to the invention have been isolated. The terms "isolated protein" or "isolated peptide" mean that the protein or peptide has been separated from its natural environment. An isolated protein or peptide may be in an essentially purified state. The term "essentially ed" means that the protein or peptide is essentially free of other substances with which it is associated in nature or in vivo.

The ng given herein with respect to specific amino acid sequences, e.g. those shown in the sequence listing, is to be construed so as to also relate to modifications, i.e. variants, of said specific sequences resulting in sequences which are functionally equivalent to said specific sequences, e.g. amino acid sequences exhibiting properties identical or similar to those of the specific amino acid sequences. One important ty is to retain g ofan antibody to its target. Preferably, a sequence modified with respect to a specific sequence, when it replaces the specific sequence in an antibody retains g of said antibody to the target. 3O It will be appreciated by those skilled in the art that in particular the sequences of the CDR sequences, hypervariable and variable regions can be modified without losing the _ 51 - ability to bind to a target. For example, CDR sequences will be either identical or highly homologous to the CDR ces specified herein.

By "highly homologous" it is plated that from 1 to 5, preferably from 1 to 4, such as 1 to 3 or 1 or 2 substitutions may be made.

The term nt" according to the invention also includes mutants, splice variants, conformations, isoforms, allelic variants, species variants and species homologs, in particular those which are naturally present. An allelic variant relates to an alteration in the normal sequence of a gene, the significance of which is often unclear. te gene sequencing often identifies numerous allelic variants for a given gene. A species homolog is a nucleic acid or amino acid sequence with a different species of origin from that of a given nucleic acid or amino acid sequence.

For the purposes of the t invention, nts" of an amino acid sequence se amino acid insertion variants, amino acid addition variants, amino acid deletion variants and/or amino acid substitution variants. Amino acid deletion variants that comprise the deletion at the N—terminal and/or C-terminai end of the protein are also called N-terminal and/or C-terminal truncation variants.

Amino acid insertion variants comprise insertions of single or two or more amino acids in a ular amino acid sequence. In the case of amino acid sequence variants having an ion, one or more amino acid residues are inserted into a particular site in an amino acid sequence, although random insertion with appropriate screening of the resulting product is also possible.

Amino acid addition variants comprise amino— and/or carboxy-terminal s of one or more amino acids, such as 1, 2, 3, 5, 10, 20, 30, 50, or more amino acids. 3O Amino acid deletion variants are characterized by the removal of one or more amino acids from the sequence, such as by removal of 1, 2, 3, 5, 10, 20, 30, 50, or more amino acids. The ons may be in any position of the protein.

Amino acid substitution ts are characterized by at least one residue in the sequence being removed and another residue being inserted in its place. Preference is given to the modifications being in positions in the amino acid sequence which are not ved between homologous proteins or peptides and/or to replacing amino acids with other ones having similar properties. Preferably, amino acid changes in protein variants are conservative amino acid changes, i.e., tutions of similarly charged or uncharged amino acids. A conservative amino acid change es tution of one of a family of amino acids which are related in their side chains. Naturally occurring amino acids are generally divided into four families: acidic (aspartate, glutamate), basic (lysine, arginine, histidine), non—polar (alanine, valine, e, isoleucine, e, phenylalanine, methionine, phan), and uncharged polar (glycine, asparagine, glutamine, cysteine, , threonine, tyrosine) amino acids. Phenylalanine, tryptophan, and tyrosine are sometimes classified jointly as aromatic amino acids.

Preferably the degree of similarity, preferably identity between a given amino acid sequence and an amino acid sequence which is a variant of said given amino acid sequence will be at least about 60%, 65%, 70%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99%. The degree of similarity or ty is given preferably for an amino acid region which is at least about %, at least about 20%, at least about 30%, at least about 40%, at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90% or about 100% of the entire length of the reference amino acid sequence. For example, if the reference amino acid sequence consists of 200 amino acids, the degree of similarity or identity is given preferably for at least about 20, at least about 40, at least about 60, at least about 80, at least about 100, at least about 120, at least about 140, at least about 160, at least about 180, or about 200 amino acids, ably continuous amino acids.

In preferred embodiments, the degree of similarity or identity is given for the entire length of the reference amino acid sequence. The alignment for determining sequence similarity, preferably sequence identity can be done with art known tools, preferably using the best sequence alignment, for example, using Align, using standard settings, preferably EMBOSS::need|e, Matrix: Blosum62, Gap Open 10.0, Gap Extend 0.5.

"Sequence similarity" indicates the percentage of amino acids that either are identical or that represent conservative amino acid substitutions. "Sequence identity" between two amino acid sequences indicates the percentage of amino acids that are identical between the sequences.

The term "percentage identity" is intended to denote a percentage of amino acid residues which are cal between the two sequences to be compared, obtained after the best ent, this percentage being purely statistical and the differences between the two ces being distributed randomly and over their entire length. Sequence comparisons between two amino acid sequences are conventionally carried out by comparing these sequences after having aligned them optimally, said comparison being carried out by segment or by "window of comparison" in order to identify and compare local regions of sequence similarity. The optimal alignment of the sequences for comparison may be produced, besides manually, by means of the local homology algorithm of Smith and Waterman, 1981, Ads App. Math. 2, 482, by means of the local homology thm of Neddleman and Wunsch, 1970, J. Mol. Biol. 48, 443, by means of the similarity search method of Pearson and Lipman, 1988, Proc. Natl Acad. Sci. USA 85, 2444, or by means of computer programs which use these algorithms (GAP, BESTFIT, FASTA, BLAST P, BLAST N and TFASTA in sin Genetics Software Package, Genetics Computer Group, 575 Science Drive, Madison, Wis.).

The percentage identity is calculated by determining the number of cal positions between the two sequences being compared, ng this number by the number of positions compared and lying the result obtained by 100 so as to obtain the tage identity between these two sequences.

Homologous amino acid sequences t according to the invention at least 40%, in particular at least 50%, at least 60%, at least 70%, at least 80%, at least 90% and 3O ably at least 95%, at least 98 or at least 99% identity of the amino acid residues.

The amino acid sequence variants described herein may readily be prepared by the WO 48489 _ 54 _ skilled person, for example, by recombinant DNA lation. The manipulation of DNA sequences for preparing proteins and es having substitutions, additions, insertions or deletions, is described in detail in Sambrook et al. (1989), for example.

Furthermore, the peptides and amino acid variants described herein may be readily prepared with the aid of known e synthesis ques such as, for e, by solid phase synthesis and similar methods.

The invention includes derivatives of the peptides or proteins described herein which are comprised by the terms "peptide" and "protein". According to the ion, "derivatives" of proteins and peptides are modified forms ofproteins and peptides. Such modifications include any chemical modification and comprise single or multiple substitutions, deletions and/or additions of any molecules associated with the protein or peptide, such as carbohydrates, lipids and/or proteins or peptides. In one ment, "derivatives" of proteins or peptides include those ed analogs resulting from glycosylation, acetylation, orylation, amidation, palmitoylation, myristoylation, isoprenylation, tion, alkylation, derivatization, introduction of protective/blocking groups, proteolytic cleavage or binding to an dy or to another cellular ligand. The term "derivative" also extends to all functional chemical equivalents of said proteins and peptides. Preferably, a modified peptide has increased stability and/or increased or decreased immunogenicity.

According to the invention, a variant, derivative, modified form, fragment, part or portion of an amino acid sequence, peptide or protein preferably has a onal property of the amino acid sequence, peptide or protein, respectively, from which it has been derived, i.e. it is functionally equivalent. In one embodiment, a variant, derivative, modified form, fragment, part or portion of an amino acid sequence, peptide or protein is immunologically equivalent to the amino acid sequence, e or protein, respectively, from which it has been derived. In one embodiment, the functional ty is an immunological property.

The term ed" means according to the invention that a particular entity, in particular a particular sequence, is present in the object from which it is derived, in _ 55 _ particular an organism or molecule. In the case of amino acid sequences, ally particular sequence regions, "derived" in particular means that the relevant amino acid sequence is derived from an amino acid sequence in which it is present.

The term "cell" or "host cell" preferably is an intact cell, i.e. a cell with an intact membrane that has not released its normal intracellular components such as enzymes, organelles, or genetic material. An intact cell preferably is a viable cell, Le. a living cell capable of carrying out its normal metabolic functions. The term "cell" includes according to the invention prokaryotic cells (e.g., E. coli) or eukaryotic cells (e.g., dendritic cells, B cells, CHO cells, COS cells, K562 cells, HEK293 cells, HELA cells, yeast cells, and insect cells). Mammalian cells are ularly preferred, such as cells from humans, mice, hamsters, pigs, goats, and primates. The cells may be derived from a large number of tissue types and include primary cells and cell lines. The term "cell" es non-cancerous cells and cancer cells such as cells of the cancer types disclosed herein.

A cell which comprises a nucleic acid molecule preferably express the e or n encoded by the nucleic acid.

"Target cell'I shall mean a cell which is a target for an immune response such as an dy. Target cells include any undesirable cell such as a cancer cell as bed herein. in preferred embodiments, the target cell is a cell expressing CLDN6. Cells expressing CLDN6 typically include cancer cells.

The terms "transgenic animal" refers to an animal having a genome comprising one or more transgenes, ably antibody heavy and/or light chain transgenes, or transchromosomes r integrated or tegrated into the animal's natural genomic DNA) and which is preferably capable of expressing the transgenes. For example, a transgenic mouse can have a human light chain transgene and either a human heavy chain transgene or human heavy chain transchromosome, such that the mouse produces human anti-CLDN6 antibodies when immunized with CLDN6 antigen and/or cells expressing CLDN6. The human heavy chain transgene can be integrated into the chromosomal DNA of the mouse, as is the case for transgenic mice, e.g., HuMAb e 56 _ mice, such as HCo7 or HCol2 mice, or the human heavy chain transgene can be maintained extrachromosomally, as is the case for transchromosomal (e.g., KM) mice as described in WO 02/43478. Such transgenic and transchromosomal mice may be capable of producing multiple isotypes of human monoclonal antibodies to CLDN6 (e.g., IgG, lgA and/or IgE) by undergoing V—D-J recombination and isotype ing.

The term "immunologically equivalent" means that the logically equivalent molecule such as the immunologically equivalent amino acid sequence exhibits the same or ially the same immunological properties and/or exerts the same or essentially the same immunological effects, e.g., with respect to the type of the immunological effect such as induction of a humoral immune reaction, the strength and/or duration of the induced immune reaction, or the specificity of the immune reaction. In the context ofthe present invention, the term "immunologically equivalent" is preferably used with respect to the logical effects or properties of a peptide or peptide variant used for immunization or an antibody. A ular immunological property is the ability to bind to dies and, where appropriate, generate an immune response, preferably by stimulating the generation of antibodies. For example, an amino acid sequence is immunologically equivalent to a reference amino acid sequence if said amino acid sequence when exposed to the immune system of a subject induces an immune reaction, preferably antibodies, having a specificity of reacting with the reference amino acid sequence, such as the reference amino acid sequence forming part of CLDN6.

The invention provides methods for detecting the presence of CLDN6 antigen in a sample, or measuring the amount of CLDN5 antigen, comprising contacting the sample, and optionally a control , with an antibody ofthe invention which binds to CLDN6, under conditions that allow for formation of a x between the antibody and CLDN6. The formation of a complex is then detected, wherein a ence in complex formation between the sample compared to a l sample is indicative for the presence of CLDN6 antigen in the sample. _ 57 _ Methods as described above are useful, in particular, for sing CLDN6-related diseases such as cancer diseases, e.g., cancer diseases as described herein. Preferably an amount of CLDN6 in a sample which is higher than the amount of CLDN6 in a reference or control sample is indicative for the presence of a CLDN6-related disease in a subject, in particular a human, from which the sample is d.

When used in s as bed above, an antibody described herein may be provided with a label that functions to: (i) provide a detectable ; (ii) interact with a second label to modify the detectable signal provided by the first or second label, e.g.

FRET (Fluorescence Resonance Energy Transfer); (iii) affect mobility, e.g. electrophoretic mobility, by charge, hydrophobicity, shape, or other physical parameters, or (iv) provide a capture moiety, e.g., affinity, antibody/antigen, or ionic complexation. Suitable as label are structures, such as fluorescent labels, luminescent labels, chromophore labels, radioisotopic labels, isotopic labels, preferably stable isotopic labels, isobaric labels, enzyme labels, le labels, in particular metal particle labels, magnetic particle labels, polymer particle labels, small organic molecules such as biotin, ligands of receptors or binding molecules such as cell adhesion proteins or lectins, label—sequences comprising nucleic acids and/or amino acid residues which can be detected by use of binding agents, etc. Labels comprise, in a nonlimiting manner, barium e, iocetamic acid, iopanoic acid, calcium ipodate, sodium diatrizoate, meglumine diatrizoate, metrizamide, sodium tyropanoate and radio stic, including positron emitters such as fluorine-18 and carbon-11, gamma emitters such as iodine-123, technetium-99m, iodine—131 and indium—111, nuclides for nuclear magnetic resonance, such as fluorine and gadolinium.

According to the ion, a ence" such as a reference sample or nce organism may be used to correlate and compare the results obtained in the methods of the ion from a test sample or test organism. Typically the nce organism is a healthy organism, in particular an organism which does not suffer from a disease such as a cancer disease. A "reference value" or ence level" can be determined from a 3O reference empirically by measuring a sufficiently large number of references. Preferably the nce value is determined by measuring at least 2, preferably at least 3, _ 5g _ preferably at least 5, preferably at least 8, preferably at least 12, preferably at least 20, preferably at least 30, preferably at least 50, or preferably at least 100 nces.

"Reduce" or "inhibit" as used herein means the ability to cause an overall decrease, preferably of 5% or r, 10% or greater, 20% or greater, more preferably of 50% or greater, and most preferably of 75% or greater, in the level. The term "inhibit" or similar phrases includes a complete or essentially complete inhibition, Le. a reduction to zero or ially to zero.

Terms such as "increase" or "enhance" preferably relate to an se or enhancement by about at least 10%, ably at least 20%, preferably at least 30%, more preferably at least 40%, more preferably at least 50%, even more preferably at least 80%, and most preferably at least 100%.

The agents, compositions and methods described herein can be used to diagnose a subject with a disease. Diseases which can be sed encompass all diseases expressing CLDN6. Particularly preferred diseases are cancer diseases such as cancer diseases described herein. 2O According to the invention, the term se" refers to any pathological state, including cancer diseases, in particular those forms of cancer es described herein.

The term "normal" such as used in the terms "normal tissue" or "normal conditions" refers to healthy tissue or the conditions in a healthy t, i.e., non-pathological conditions, wherein "healthy" preferably means non—cancerous.

"Disease involving cells expressing CLDN6" means according to the invention that CLDN6 is expressed in cells of a diseased tissue or organ. In one embodiment, expression of CLDN6 is increased compared to the state in a healthy tissue or organ. An increase refers 3O to an increase by at least 10%, in particular at least 20%, at least 50%, at least 100%, at least 200%, at least 500%, at least 1000%, at least 10000% or even more. In one embodiment, sion is only found in a diseased tissue, while expression in a healthy c 59 _ tissue is repressed. According to the ion, diseases involving or being associated with cells expressing CLDN6 include cancer diseases, in particular those forms of cancer described herein. ing to the invention, the term "tumor" or "tumor disease" refers to a swelling or lesion formed by an abnormal growth of cells (called neoplastic cells or tumor cells). By "tumor cell" is meant an abnormal cell that grows by a rapid, uncontrolled cellular eration and continues to grow after the stimuli that initiated the new growth cease.

Tumors show partial or complete lack of structural organization and functional coordination with the normal tissue, and y form a distinct mass of tissue, which may be either benign, pre-malignant or malignant.

A benign tumor is a tumor that lacks all three of the malignant properties of a cancer.

Thus, by definition, a benign tumor does not grow in an ted, aggressive manner, does not invade nding tissues, and does not spread to non-adjacent tissues (metastasize). Common examples of benign tumors include moles and uterine fibroids.

The term "benign" implies a mild and gressive disease, and indeed, many kinds of benign tumors are ss to the health. However, some neoplasms which are defined as "benign tumors" because they lack the invasive properties of a cancer, may still produce negative health effects. Examples of this include tumors which produce a "mass effect" (compression of vital organs such as blood vessels), or "functional" tumors of endocrine tissues, which may overproduce certain hormones (examples include thyroid adenomas, adrenocortical adenomas, and pituitary adenomas).

Benign tumors typically are nded by an outer e that inhibits their ability to behave in a malignant manner. In some cases, certain "benign" tumors may later give rise to malignant cancers, which result from additional genetic changes in a subpopulation ofthe tumor‘s neoplastic cells. A prominent example ofthis phenomenon is the tubular adenoma, a common type of colon polyp which is an important precursor to colon cancer. The cells in tubular adenomas, like most tumors which ntly progress to cancer, show certain abnormalities of cell maturation and appearance _ 6O _ collectively known as dysplasia. These cellular alities are not seen in benign tumors that rarely or never turn cancerous, but are seen in other pre-cancerous tissue abnormalities which do not form discrete masses, such as pre—cancerous lesions of the e cervix. Some authorities prefer to refer to dysplastic tumors as "pre-malignant", and reserve the term "benign" for tumors which rarely or never give rise to cancer.

Neoplasm is an abnormal mass oftissue as a result of neoplasia. Neoplasia (new growth in Greek) is the abnormal eration of cells. The growth of the cells exceeds, and is uncoordinated with that ofthe normal tissues around it. The growth persists in the same excessive manner even after cessation of the stimuli. It usually causes a lump or tumor.

Neoplasms may be benign, pre—malignant or malignant.

"Growth of a tumor" or "tumor growth" according to the invention relates to the tendency of a tumor to increase its size and/or to the tendency of tumor cells to proliferate.

Cancer (medical term: malignant neoplasm) is a class of diseases in which a group of cells display uncontrolled growth (division beyond the normal limits), invasion (intrusion on and ction of nt tissues), and sometimes metastasis (spread to other locations in the body via lymph or blood). These three malignant properties of cancers differentiate them from benign , which are self-limited, and do not invade or metastasize. Most cancers form a tumor but some, like ia, do not. According to the invention, the terms "cancer" and "tumor" or "cancer disease" and "tumor disease" are generally used interchangeably herein to refer to diseases wherein cells display an uncontrolled growth and optionally invasion and/or asis.

Preferably, a "cancer disease" according to the invention is characterized by cells expressing CLDN6. A cell expressing CLDN6 preferably is a cancer cell, preferably of the tumors and cancers described herein. Preferably, such cell is a cell other than a placenta cell. c. 61 _ Cancers are classified by the type of cell that resembles the tumor and, therefore, the tissue presumed to be the origin ofthe tumor. These are the ogy and the location, respectively.

The term "cancer" according to the invention ses leukemias, mas, melanomas, teratomas, lymphomas, neuroblastomas, gliomas, rectal cancer, endometrial , kidney cancer, adrenal cancer, thyroid cancer, blood cancer, skin cancer, cancer ofthe brain, cervical cancer, intestinal cancer, liver cancer, colon cancer, stomach cancer, intestine cancer, head and neck cancer, gastrointestinal cancer, lymph node , esophagus cancer, colorectal cancer, pancreas cancer, ear, nose and throat (ENT) cancer, breast cancer, prostate cancer, cancer of the uterus, ovarian cancer and lung cancer and the metastases thereof. Examples thereof are lung carcinomas, mamma carcinomas, prostate omas, colon carcinomas, renal cell carcinomas, cervical carcinomas, or metastases of the cancer types or tumors described above. The term cancer ing to the invention also comprises cancer metastases.

The main types of lung cancer are small cell lung carcinoma (SCLC) and all cell lung carcinoma (NSCLC). There are three main sub—types of the non-small cell lung carcinomas: squamous cell lung carcinoma, adenocarcinoma, and large cell lung carcinoma. Adenocarcinomas account for approximately 10% of lung cancers. This cancer usually is seen peripherally in the lungs, as opposed to small cell lung cancer and squamous cell lung cancer, which both tend to be more lly located.

According to the invention, a noma" is a malignant tumor derived from epithelial cells. This group represents the most common cancers, ing the common forms of breast, prostate, lung and colon cancer.

"Adenocarcinoma" is a cancer that originates in glandular tissue. This tissue is also part of a larger tissue category known as epithelial tissue. Epithelial tissue includes skin, glands and a variety of other tissue that lines the cavities and organs of the body.

Epithelium is derived embryologically from ectoderm, endoderm and mesoderm. To be classified as adenocarcinoma, the cells do not necessarily need to be part of a gland, as _ 62 _ long as they have ory properties. This form of carcinoma can occur in some higher s, including humans. Well differentiated adenocarcinomas tend to resemble the lar tissue that they are derived from, while poorly entiated may not. By staining the cells from a biopsy, a pathologist will determine whether the tumor is an adenocarcinoma or some other type of . Adenocarcinomas can arise in many tissues of the body due to the ubiquitous nature of glands within the body. While each gland may not be secreting the same substance, as long as there is an exocrine function to the cell, it is considered glandular and its ant form is therefore named adenocarcinoma. Malignant adenocarcinomas invade other tissues and often metastasize given enough time to do so. Ovarian adenocarcinoma is the most common type of ovarian carcinoma. It includes the serous and mucinous adenocarcinomas, the clear cell adenocarcinoma and the trioid adenocarcinoma.

By "metastasis" is meant the spread of cancer cells from its original site to another part of the body. The formation of metastasis is a very complex process and depends on detachment of malignant cells from the primary tumor, invasion of the extracellular matrix, penetration of the endothelial basement membranes to enter the body cavity and vessels, and then, after being transported by the blood, infiltration of target organs.

Finally, the growth of a new tumor, Le. a secondary tumor or metastatic tumor, at the target site depends on angiogenesis. Tumor metastasis often occurs even after the removal of the primary tumor because tumor cells or components may remain and develop metastatic ial. In one embodiment, the term tasis" according to the invention relates to "distant metastasis" which relates to a metastasis which is remote from the primary tumor and the regional lymph node system.

The cells of a secondary or metastatic tumor are like those in the original tumor. This means, for example, that, if ovarian cancer metastasizes to the liver, the ary tumor is made up of abnormal ovarian cells, not of abnormal liver cells. The tumor in the liver is then called metastatic ovarian , not liver cancer.

A relapse or recurrence occurs when a person is affected again by a condition that affected them in the past. For example, if a patient has suffered from a cancer disease, _ 63 _ has received a successful treatment of said disease and again develops said e said newly developed disease may be considered as relapse or recurrence. However, according to the invention, a relapse or recurrence ofa cancer disease may but does not necessarily occur at the site of the original cancer disease. Thus, for example, if a patient has suffered from ovarian tumor and has received a successful treatment a relapse or recurrence may be the occurrence of an ovarian tumor or the occurrence of a tumor at a site different to ovary. A relapse or recurrence of a tumor also includes situations wherein a tumor occurs at a site different to the site of the original tumor as well as at the site of the original tumor. Preferably, the original tumor for which the patient has received a treatment is a primary tumor and the tumor at a site ent to the site of the original tumor is a secondary or metastatic tumor.

By " is meant to administer a nd or composition to a subject in order to prevent or eliminate a e, including reducing the size of a tumor or the number of tumors in a subject; arrest or slow a disease in a subject; inhibit or slow the development of a new disease in a subject; decrease the frequency or ty of symptoms and/or ences in a subject who tly has or who previously has had a disease; and/or prolong, i.e. se the lifespan ofthe subject. 2O In ular, the term "treatment of a disease" includes curing, shortening the duration, ameliorating, preventing, slowing down or inhibiting progression or worsening, or preventing or delaying the onset of a disease or the symptoms thereof.

By "being at risk" is meant a subject, Le. a patient, that is identified as having a higher than normal chance of developing a disease, in particular , compared to the general population. In addition, a subject who has had, or who currently has, a e, in particular cancer is a subject who has an increased risk for developing a disease, as such a subject may continue to develop a disease. Subjects who currently have, or who have had, a cancer also have an increased risk for cancer ases.

The term "immunotherapy" relates to a treatment involving a specific immune reaction. _ 64 - in the context of the present invention, terms such as "protect", "prevent", "prophylactic", ntive", or "protective" relate to the prevention or treatment or both of the occurrence and/or the ation of a disease in a subject and, in particular, to minimizing the chance that a subject will p a disease or to delaying the development of a disease. For example, a person at risk for a tumor, as bed above, would be a candidate for therapy to prevent a tumor. Immunotherapy may be performed using any of a variety of techniques, in which agents function to remove antigen-expressing cells from a patient.

Within certain embodiments, immunotherapy may be active immunotherapy, in which treatment relies on the in vivo stimulation of the endogenous host immune system to react against ed cells with the administration of immune response-modifying agents (such as immunoreactive peptides and nucleic acids).

Within other embodiments, immunotherapy may be passive immunotherapy, in which treatment involves the delivery of agents with ished tumor—immune reactivity (such as antibodies) that can directly or indirectly mediate antitumor effects and does not necessarily depend on an intact host immune system.

The term "in vivo" relates to the situation in a subject.

The terms "subject", idual", "organism" or "patient" are used interchangeably and relate to vertebrates, preferably mammals. For example, mammals in the context of the t invention are humans, non—human primates, domesticated animals such as dogs, cats, sheep, cattle, goats, pigs, horses etc., laboratory animals such as mice, rats, rabbits, guinea pigs, etc. as well as animals in captivity such as s of zoos. The term "animal" as used herein also includes humans. The term "subject" may also include a t, i.e., an , preferably a human having a disease, preferably a disease as described herein.

According to the invention, a "sample" may be any sample useful according to the present invention, in particular a biological sample such a tissue sample, including body _ 65 _ fluids, and/or a cellular sample and may be obtained in the conventional manner such as by tissue biopsy, including punch biopsy, and by taking blood, bronchial aspirate, sputum, urine, feces or other body fluids. According to the invention, the term "sample" also includes processed samples such as fractions or isolates of biological samples, e.g. nucleic acid and peptide/protein isolates. Preferably a sample contains cells or tissue of the organ which is to be examined, e.g. which is to be diagnosed for cancer. For example, ifthe cancer to be diagnosed is lung cancer a sample may contain cells or tissue ed from lung.

According to the invention a sample may be a sample such as a bodily sample derived from a patient containing or being expected of ning tumor or cancer cells. The bodily sample may be any tissue sample such as blood, a tissue sample obtained from the primary tumor or from tumor metastases or any other sample containing tumor or cancer cells.

The present ion is described in detail by the figures and examples below, which are used only for ration purposes and are not meant to be ng. Owing to the description and the es, further embodiments which are likewise included in the invention are accessible to the skilled worker.

Figures: Figure 1A: Sequence alignment of claudin 6 and claudin 9 proteins (human/murine) The sequence alignment shows the high homology between human and mouse claudin 6 and human n 9.

Figure 18: Sequence alignment of claudin 6 and claudin 3, 4 and 9 proteins (human) The sequence alignment shows the high homology in the n multigene family Figures 2 A and B: Specificity of antibodies tested in WesternBlot analysis 3O Cell lysates of HEK293 cells ected with mock, human CLDN3, 4, 6 or 9 and CLDN6 positive tumor cells (PA-1 SC12 and NEC—8) were blotted and bound antibodies (rabbit- anti—CLDN3 (lnvitrogen) 0.5 pg/mL, mouse-anti-CLDN4 (lnvitrogen) 1 pg/mL, rabbit—anti- _ 66 _ CLDN6 (IBL) 0.2 pg/mL, goat-anti—CLDN9 (Santa Cruz) 0.4 ug/mL or the onal mouse antibodies (5 pg/mL) were detected by Peroxidase-conjugated secondary antibodies.

Figure 3: Histological analysis of Western Blot positive antibodies Binding of lead mumAB 58-1B, 58—3A and 58—4B in comparison to rb-anti-CLDN6 lBL antiserum to FFPE sections of ovarian cancer.

Figure 4A: Epitope Mapping using synthetic pping peptides Overlapping peptides were immobilized onto microtiter plates and antibodies were added. Bound antibodies were developed with appropriate peroxidase conjugated secondary ts.

Figure 4B: Epitope Mapping using ylated synthetic overlapping peptides Highly overlapping peptides N-terminally biotinylated via a flexible hydrophilic linker were synthesized and loaded onto vidin coupled microtiter plates. Antibodies (1 ug/mL) were applied and bound antibodies were detected and analysed.

For comparison of signal ities of mumAB 2 to rb-serum (IBL) maximal binding of antibodies to C—term peptide 19 was defined as 100%. g intensity of each antibody to one peptide was calculated relative to maximal binding for each test system.

Binding of mumABs was analysed in 3 independent experiments in triplicates Binding of IBL—serum was analysed in 2 independent ments in triplicates Figure 4C: Binding site of monoclonal lead 58-4B-2 and polyclonal iCLDNG-serum (IBL).

Figure 5: Sequences of the antibodies 58-13, 58-3A and 58-4B Figure 6: Background signals of different antibodies on normal ovarian tissue Comparison of the lead antibodies mumAB 58-1B, 58-3A and 58-4B versus the commercial IBL antibody on normal ovarian tissue ody concentration Bug/ml; clinic—like protocol).

WO 48489 Examples The techniques and methods used herein are described herein or carried out in a manner known per se and as described, for example, in Sambrook et al., Molecular Cloning: A Laboratory Manual, 2nd Edition (1989) Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. All methods including the use of kits and reagents are carried out according to the manufacturers’ information unless specifically indicated.

Example 1: Materials and Methods g of antibody binding site (Figure 4A) Mapping of epitopes recognized by antibodies can be performed as described in detail in "Epitope Mapping Protocols (Methods in Molecular Biology) by Glenn E. Morris ISBN- —375—9 and in "Epitope Mapping: A Practical Approach" Practical Approach Series, 248 by Olwyn M. R. Westwood, Frank C. Hay.

Epitope mapping with biotinylated peptides e 4B) A Peptide—ELISA was performed to identify the dy—binding site of onal murine lead antibodies and polyclonal rb-serum from lBL. Biotinylated overlapping peptides covering the C-terminal sequence of CLDN6 were coupled to SA coated plates.

Purified mumAB (lug/ml) or IBL rb—serum (lug/ml) were applied to antigen coated ELISA—plates and unbound antibodies were washed off. Bound antibodies were detected with corresponding enzyme—labeled secondary antibody ine phosphatase goat anti—mouse lgG(1+2a+2b+3) or alkaline atase goat anti-rabbit lgG F(ab)2) and ABTS enzyme substrate and signal ities are analysed.

For comparison of signal intensities of mumAB 58-48—2 to rb-serum (IBL) maximal binding of antibodies to C-term e19 was defined as 100%.

Binding intensity of each antibody to one peptide was ated in relation to maximal binding for each test system (mouse or rabbit) independently. 3O Binding of mumABs were analysed in 3 independent experiments in cates Binding of IBL-serum was analysed in 2 independent experiments in triplicates _ 68 _ Isotype determination To determine the isotype of purified antibodies, the IsoStrip Mouse Monoclonal Antibody Isotyping Kit (Roche, Cat. No. 1493027) was used as described by the manufacturer.

Western Blot Newly generated Anti-CLDN6 lgG can be further tested for specific binding to CLDNG antigen by Western Blotting. Briefly, cell extracts from cells expressing CLDN3, 4, 6 or 9 and appropriate negative controls can be prepared and subjected to sodium dodecyl sulfate (SDS) polyacrylamide gel electrophoresis. After electrophoresis, the separated antigens will be erred to nitrocellulose membranes, blocked, and probed with the monoclonal antibodies to be . lgG binding can be detected using anti—mouse lgG peroxidase and developed with ECL substrate. ogy histochemistry (lHC) was performed on slides of 4% buffered formalin fixed paraffin embedded tissue s. Paraffin embedding was performed ing to standard ols.

After deparaffinization and ation, all slides were subjected to antigen retrieval by 2O boiling in 0.1 M Tris/ 0.01 M EDTA buffer supplemented with 15mM sodium azide (pH 9.0) at 95—98°C for 30 min, and subsequently endogenous dases were quenched by adding 3% H202 supplemented with 15 mM NaNg. After washing with 150mM sodium chloride buffer (pH 7.6) supplemented with 0.05% (w/v) Tween-20 and 0.005% (w/v) Proclin, the slides were incubated with 1.0 or 5.0 ug/ml diagnostic monoclonal mouse anti-CLDN6 antibody 58—43 at room temperature for one hour. Antibody binding was visualized using ready-to-use solution containing a polymer—based horseradish~ peroxidase-labeled secondary antibody (Histofine MAX PO (M)/ UIO MAX PO (M), Nichirei, Japan). Sections were uently counter—stained with Mayer’s haematoxylin (Carl Roth GmbH, Karlsruhe, Germany) and subjected to evaluation by the 3O raters.

Histological assessment - 69 _ All samples were analyzed ing the relative proportion of positive stained tumour cells in relation to all e tumour cells for each section. The intensity of the staining was classified as ve (-), weakly positive (1+), medium positive (2+) and strongly positive (3+). Only membranous ng was considered as positive. Ovarian cancer tissue served as positive control for each staining. Additionally embryonic kidney tissue of New Zealand White rabbits on day 29 of the gestation period was found to show a strong ve staining intensity. This was used as al staining intensity reference for staining positivity (2+ - 3+).

Example 2: Generation of monoclonal antibodies The aim of this project was to generate murine onal CLDN6—specific antibodies capable of detecting CLDN6 expressing tumour cells in ovarian cancer or any other cancer tissue of any histology including primary neal or fallopian tube tumours FFPE tissues.

To generate a highly specific, high affinity diagnostic CLDN6 antibody it was essential to start immunization ols with a variety of different immunogens (Table 1) and adjuvants. During the project about 130 mice (C57BL/6 and BALB/c) were subjected to various immunization strategies to trigger an a—CLDN6 immune response (Table 2).

To trigger the mouse immune system and to overcome the immune tolerance we used peptide—conjugates and recombinant proteins coding for different parts of human CLDN6 expressed as recombinant fusion proteins with different epitopes to tate affinity purification (Polyhistidine-(HIS)- and G|utathion—S—transferase—(GST)—tag) (Table Out of 20 different immunization gies the best results were achieved by treating mice with GST—tagged CLDN6 C-terminal recombinant protein (Table 2) in combination with various adjuvants (Table 2). _ 70 _ On the day of fusion, mouse splenocytes were isolated and fused to the mouse myeloma cell line P3X63Ag8.653 . For fusion of mouse cells to the myeloma cell line we followed the standard protocol published by Kohler and Milstein 1975. After hypoxanthine-aminopterin-thymidine (HAT) selection, supernatants were tested in ELISA for secretion of antibodies recognizing the antigen used for immunizations. 69 fusions were performed and more than 25 000 hybridoma cell clones were screened.

The hybridoma cells of ELISA positive supernatants (402) were subcloned to generate monoclonal hybridomas. Supernatants of the ned oma cells were rescreened in ELISA for binding to Claudin6 n. Hybridoma cells of 88 positive clones (binding to antigen but not to backbone or tag) were expanded and supernatants analyzed further in Western Blot for their specificity.

The three lead candidates (58—4B, 58-lB and 58—3A) resulted from a 11 step- immunization strategy (Immunization #10 for 123 days). Three days before splenectomy, the mice were boosted to activate the targeted B—cells ed by fusion 58 (Table 3).

Example 3: Western Blot Screening of monoclonal antibodies To test if ELISA—positive antibodies in the supernatants are able to bind specifically to recombinant n 6they were analysed in Western Blot. Antibodies binding to CLDN6 but not to any other tagged—protein were purified and cells expanded and cryoconserved. dies were purified via FPLC using MABselect Protein A affinity resin. The purified antibodies selected by the Western Blot screening were reanalyzed in Western Blot to assess the binding to CLDN6 positive tumour cell lines (PA—1, NEC-8) and to CLDN3, 4, 6 or 9 transfected HEK293 cells (Figure 2). In addition, the antibodies were evaluated for their ability to bind their antigen in formalin fixed in- embedded tissues (FFPE) by histochemistry. Supernatants of 33 hybridoma specifically g to Claudin 6 were purified and analysed further in Immunohistochemistry.

Example 4: Histological analysis of Western Blot positive antibodies The aim of this experiment was to test the CLDN6 specificity and sensitivity of the antibodies. This was done by using CLDN6 expressing FFPE ovarian cancer tissues (Figure In a first experiment the purified antibodies that were tested positive in the 1St Western Blot-Screen, were analyzed at a concentration of 1 ug/ml and Spg/ml on ovarian cancer FFPE sections. A laboratory standard and established ght ng ol with Citric retrieval buffer and a retrieval temperature of 120°C was used. Antibodies showing tissue specific CLDN6 staining without producing high levels of unspecific background staining were further ed to 0.2, 1, 2 and 5 ug/ml on various ovarian cancer tissues to further evaluate the sensitivity and specificity of these antibodies. In the following development stages the newly generated dies were tested directly at higher concentrations of 1 and 5 ug/ml because the differences in staining intensities of the different antibodies could not be clearly evaluated at a tration of 0.2 ug/ml.

Antibodies generating strong signals on the cell nes of ovarian tumour tissue of the selected tissues and little to no background on the adjacent healthy tissues were selected for further ion experiments and specificity analysis. The following three antibodies fulfilled these criteria and were selected as lead candidates for further investigation: 58—18, 58—3A and 58-48.

Example 5: Epitope mapping of the mumAbs (Figure 4) Peptide ELISA was performed to identify the antibody—binding epitopes on CLDN6. Each ed antibody was tested on peptides overlapping 11aa covering the C—terminal ce of CLDN6. Antibodies 46—5A, 58—1B, 58-3A, 58-48 and 58—93 showed specific binding to an epitope covered by the peptide AISRGPSEYPTKNYV (Peptide 7; Figure 4A).

The binding site of these antibodies was further terized using biotinylated 3O peptides overlapping by 14 out of 15 aa.

Surprisingly, dies 58—18, 58—3A and 58-48 and subclone 58-4B—2 binding to the sequence EYPTKNY (Figure 4B) are able to bind to CLDN6 in FFPE cancer tissues very _ 72 _ specifically with low background. In contrast, the antibody 46-5A was able to bind to peptides not comprising the sequence EYPTKNY but comprising a portion thereof, i.e. the sequence EYPTK e 4B). Commercially available i—CLDN6 onal antiserum (lBL) binds to peptides comprising the sequence RGPS (Figure 4C).

Example 6: Analysis of antibody specificity using a normal tissue panel Antibodies ing strong signals on the tested ovarian cancer tissue (58-1B, 58-3A and 58—4B) with the tory standard and established staining protocol were further analyzed on various, relevant normal, g healthy donor s (e.g. lung, testis, uterus und ovar) to ensure the high CLDN6 target specificity. Staining of these selected s was performed using the laboratory standard and established staining protocol (overnight; 120°C retrieval temperature, citric retrieval buffer).

None ofthe three selected antibodies generated unspecific staining signals on the tested normal tissue panel, except of a faint unspecific signals in a single peripheral region of one ovarian tissue sample. This weak signal was only visible at the higher of both tested trations (1 & 5 , not representing an ovarian substructure.

Example 7: Comparison of antibody sensitivity using ovarian cancer and normal tissue 2O panel samples No significant differences in the staining pattern and staining intensities of the antibodies 58-3A, 58-lB and 58-4B were visible in the previous experiments. ore the antibodies were subjected to staining experiments with a more clinically oriented, meaning more time efficient, staining protocol. To simulate the staining ses applied in standard pathology laboratories, a One—Day-Protocol with an 1 hour primary antibody incubation step and a water bath (98°C) retrieval step was established. In addition, two different retrieval buffers were compared to test whether the different retrieval conditions could nce the sensitivity of the tested antibodies regarding CLDN6 detection.

For all antibodies more intense s and a higher amount of positive stained tumour cells were generated with the adapted One—Day-Protocol with Tris-buffer for retrieval, _ 73 _ compared to the standard citric retrieval . Most intense staining signals were generated with 58-4B reaching up to 80% of 3+ stained tumor cells, s the staining intensities of the candidate 58—18 were the least intense reaching only 30% of 3+ stained tumor cells.

The staining protocol with the Tris-buffer for retrieval resulting in the most ive staining s was subsequently applied for the staining of the normal tissue panel to test the specificity of the selected antibodies under routine clinical laboratory ions.

The best results in respect to CLDN6-specificity and sensitivity in FFPE-tissues were achieved by using the 58-4B diagnostic antibody candidate. No signals were able on the normal tissues. All other antibodies generated signals on Reinke ls of the testis sample. In addition the 58—3A antibody generated weak staining on blood vessels.

The 58-18 antibody demonstrated more intense signals (1+) on testis, and ovarian normal tissues.

In all analyzed samples the mumAb 58—4B demonstrated better performance in respect of showing no background staining and intense staining on relevant tumour tissue, whereas mumAb 58-3A and 58—1B candidates showed intense staining on relevant tumour tissue but with higher background signals. Especially the signals produced using mumAb 58-1B were of high intensity but with the drawback of high background staining.

For the later use in a al setting the ponding hybridoma for generation of the diagnostic antibody candidates were adapted to serum free media. Unfortunately the adaption of clone 58-3A to serum-free ions wasn’t possible. Therefore the antibody candidate 58—3A was also excluded from further ogical studies, leaving 58—4B as the final lead candidate. e 8: Histological in depth analysis and antibody characterization 3O In a first step, the 58-4B antibody lot produced under serum free conditions was ed with the antibody lot produced under serum conditions using a normal tissue panel TMA (MN0961) in order to detect differences in the target-sensitivity and — _ 74 _ specificity between the lots. The staining was performed using a clinic like, One-Day— Protocol (waterbath retrieval, Tris-buffer for retrieval) with y—free components.

With both antibody lots, faint stainings were detected in some normal tissue samples (see Table 4). ed with the antibody produced under serum conditions, the serum—free antibody lot was cleaner with less artificial spots on the analysed samples.

On testis, staining signals were visible on Reinke crystals with both antibody lots.

In a second step, the serum-free produced antibody was tested on an ovarian cancer TMA panel and compared with the commercially ble IBL antibody. This commercial antibody had already been used in previous study stainings. The polyclonal IBL antibody was used with the study ol (overnight, 120°C retrieval temperature, citric retrieval buffer). The 58—4B dy was used with the e clinic like protocol (One-Day— ol, waterbath val, Tris buffer for retrieval).

Of the 72 spotted TMA ovarian cancer cases just one sample was positive with the IBL dy. In contrast 14/72 samples were tested positive for CLDN6 when stained with the 58—4B antibody.

Unfortunately the quality of the commercial Ovarian Cancer TMA samples was low, resulting in weak staining signals on positive tumour samples. ore the comparison was repeated with tumour resection specimens from Dr. Dhaene, representing larger tumour regions with a high quality conservation of lung, uterine and testicular tumour samples.

The 58—4B staining resulted in a more sensitive and specific detection of CLDN6 in tumour samples compared to the stainings performed with the polyclonal IBL antibody, meaning more tumour cells were positive and a stronger intensity of the stained tumour cells was detected.

Example 9: Sequence analysis of the lead antibodies An analysis of the sequence ofthe antibodies 58-1B, 58—3A and 58—4B is shown in Figure and below. _ 75 _ Amino acid sequence analysis of 58-4B-2 lead antibody Heavy EVQLQQSGTVLARPGASVRMSCRTSGYIFTTYWIHWVKERPGQG IFPGNS chain DTTYNQKFRG VTSASTAYLDLSSLTDEDSAWYCTREFYATWGQGTTLTVSS Light DlVLTQN PLTLSVTIGQTASISCKSSQNLLYSDGKTYLNWLLQRPGQSPKRLIYLMSKL chain DSGVPDRFTGSGSGTDFTLKlSRVEAEDLGVYYCWQGTHFPWTFGGGTKLENT Amino acid sequence analysis of 58-1B antibody EVQLQQSGTVLARPGASVKMSCRTSGYTFTTYWMHWVRERPGQGLEWIGAIYPEN SDATYNQKFKGKASLTAVTSASTAYLELSSLTDEDSAVYYCTREFYATWGQGTTLTVS DVVMTQNPLTLSVTIGQTASISCKSSQNLLYSDGKTYLNWLLQRPGQSPKRLIYLMSK LDSGVPDRFTGSGSRTDFTLKISRVEAEDLGVYYCWQGTHFPWTFGGGTKLEIT Amino acid sequence analysis of 58-3A antibody Heavy EVQLQQSGTVLARPGASVKMSCRTSGYTFTTYWMHWVRERPGQGLEWIGAIYPEN chain SDATYNQKFKGKASLTAVTSASTAYLELSSLTDEDSAVYYCTREFYATWGQGTTLTVS Light DIVLTQN PLTLSVTIGQTASISCKSSQN LLYSDGKTYLNWLLQRPGQSPKRLIYLMSKLE chain SGVPDRFTGSGSGTEFTLKISRVEAEDLGVWCWQGTHFPWTFGGGTKLEIS m_ I maui xddmz>u <3" mm I+>>Zv:.n>mmm m3.._.mu+>>2x._.m>mmn_ I III Bm<_>_>=mn_ wasp— zztnzw ignomuummubujuwu Eafimauzmzéflfima a:__<_._<.:SU>n__._._.._>_.um_>u_>_0m._.._>._mm<_2>:ma .CDEF: E .Q._ mung—gum muhbu wdeUmn—Uhuu m>u._._.uv_< $52.35 .0 0:68 0:68 9.38 9.536 won #33 com 5.. 8TRH<< 263:2 o-.~m.n<< ONN-NwH<< NOTNQHE cot—23% mammocsEE_ mummico: 23322 mm". _._._v_ _._._v_ ._. 33330 g 1:333". _._§-~mu_a$ I§-mw_§a& :mmo::EE. H m 34m: mgmu win» cozmucafiz...

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Claims (23)

Claim:

1. An antibody or antigen-binding fragment thereof, which binds: (i) to a peptide having the amino acid sequence EYPTKNY (SEQ ID NO: 38), and/or (ii) to claudin 6 (CLDN6), wherein said antibody or antigen-binding fragment thereof binds to CLDN6 by binding at least to an epitope within CLDN6 having the amino acid sequence EYPTKNY (SEQ ID NO: 38), and/or (iii) to a peptide having the amino acid sequence EYPTKNYV (SEQ ID NO: 29), and/or (iv) to claudin 6 (CLDN6), wherein said antibody or antigen-binding fragment thereof binds to CLDN6 by binding at least to an epitope within CLDN6 having the amino acid sequence EYPTKNYV (SEQ ID NO: 29), and/or (v) to a peptide having the amino acid sequence AISRGPSEYPTKNYV (SEQ ID NO: 15), wherein the antibody or antigen-binding fragment thereof does not bind to a peptide having the amino acid sequence TSAPAISRGPSEYPT (SEQ ID NO: 14), and/or (vi) to claudin 6 (CLDN6), n said antibody or antigen-binding fragment thereof binds to CLDN6 by binding at least to an epitope within CLDN6 having the amino acid sequence AISRGPSEYPTKNYV (SEQ ID NO: 15), wherein the antibody or antigen-binding fragment thereof does not bind to a peptide having the amino acid sequence SRGPSEYPT (SEQ ID NO: 14).

2. The dy or antigen—binding fragment thereof of claim 1, n said CLDN6 is cell e membrane-bound CLDN6.

3. The antibody or antigen—binding fragment thereof of claim 1 or 2, wherein said CLDN6 is present on cancer cells.

4. The antibody or antigen-binding fragment thereof of claim 3, wherein said cancer cells are CLDN6 sing cancer cells.

5. The antibody or antigen—binding fragment thereof of claim 3 or 4, wherein said cancer cells are ed from the group consisting of n, ular, stomach, breast, atic, lung, uterine, and urinary r cancer cells.

6. The antibody or antigen-binding fragment thereof of claim 3 or 4, wherein said cancer cells are atic cancer cells.

7. The dy of any one of claims 1 to 5 which is a chimeric, human or zed antibody.

8. The antibody of any one of claims 1 to 7, which is a monoclonal antibody.

9. A onal dy or antigen—binding fragment thereof which (i) binds to a e having the amino acid sequence AISRGPSEYPTKNYV (SEQ ID NO: 15) and/or (ii) binds to claudin 6 (CLDN6), wherein said antibody or antigen-binding fragment thereof binds to CLDN6 by binding at least to an epitope within CLDN6 having the amino acid sequence AISRGPSEYPTKNYV (SEQ ID NO: 15).

10. An antibody or antigen—binding fragment thereof, which binds to one or more, preferably all, of the following peptides: PAISRGPSEYPTKNY (SEQ ID NO: 22), AISRGPSEYPTKNYV (SEQ ID NO: 15), ISRGPSEYPTKNYV (SEQ ID NO: 23), SRGPSEYPTKNYV (SEQ ID NO: 24), RGPSEYPTKNYV (SEQ ID NO: 25), GPSEYPTKNYV (SEQ ID NO: 26), PSEYPTKNYV (SEQ ID NO: 27), SEYPTKNYV (SEQ ID NO: 28), and EYPTKNYV (SEQ ID NO: 29), wherein the antibody or antigen—binding fragment thereof does not bind to a peptide having the amino acid sequence TSAPAISRGPSEYPT (SEQ ID NO: 14).

11. The antibody or antigen—binding fragment thereof of claim 10, wherein the difference in binding affinity to the peptide to which the antibody or antigen binding fragment binds with the lowest affinity and to the peptide to which the antibody or antigen binding fragment binds with the highest affinity is 50% or less.

12. An antibody selected from the group consisting of: (i) an antibody produced by or obtainable from a clone deposited under the accession no. DSM ACC3313 (58—1B), DSM ACC3312 (58—3A) or DSM ACC3311 -2), (ii) an antibody which is a chimerized or humanized form of the antibody under (i), (iii) an antibody which competes for CLDN6 binding with an antibody under (i), (iv) an antibody which has the specificity of the antibody under (i), (v) an antibody comprising the n binding portion or antigen binding site of the antibody under (i), or an antigen-binding fragment of the antibody under any one of (i) to (V).

13. The antibody of claim 12, wherein the antigen g portion or antigen binding site of the antibody under (i) comprises the le region of the dy under (i).

14. A conjugate comprising an antibody or antigen-binding fragment of any one of claims 1 to 13 coupled to at least one detectable label.

15. A hybridoma capable of producing the antibody of any one of claims 1 to 13.

16. A hybridoma deposited under the accession no. DSM ACC3313 (58—lB), DSM 2 (SS—3A) or DSM ACC3311 (58-4B).

17. A method for detecting CLDN6 or determining the quantity of CLDN6 in a sample comprising the steps of: (i) contacting a sample with the antibody or antigen-binding nt of any one of claims 1 to 13 or the conjugate of claim 14 and (ii) detecting the formation of a complex or determining the quantity of a complex between the antibody, the antigen-binding fragment or the ate and CLDN6.

18. A method for determining whether cells express CLDN6 comprising the steps of: (i) contacting a cellular sample with the antibody or antigen-binding fragment of any one of claims 1 to 13 or the conjugate of claim 14 and (ii) ing the formation of a complex between the antibody, the antigen-binding fragment or the conjugate and CLDN6 expressed by cells in said sample.

19. A method for diagnosis, detection or monitoring of cancer comprising the steps of: (i) contacting a biological sample with the antibody or antigen—binding fragment of any one of claims 1 to 13 or the conjugate of claim 14 and (ii) detecting the formation of a x and/or determining the quantity of a complex between the antibody, the n—binding fragment or the conjugate and CLDN6.

20. A method for determining whether a cancer is treatable by a cancer therapy targeting CLDN6 sing the steps of: (i) contacting a sample comprising cancer cells with the antibody or antigen-binding fragment of any one of claims 1 to 13 or the conjugate of claim 14 and (ii) detecting the ion of a complex between the antibody, the antigen-binding fragment or the conjugate and CLDN6.

21. A method for determining the sis of a patient having cancer comprising the steps of: (i) contacting a sample comprising cancer cells with the dy or n~binding fragment of any one of claims 1 to 13 or the conjugate of claim 14 and (ii) detecting the formation of a complex between the antibody, the antigen-binding fragment or the conjugate and CLDN6.

22. The antibody or antigen—binding fragment of any one of claims 1 to 13, the conjugate of claim 14, the hybridoma of claim 15 or 16, or the method of any one of claims 17 to 21, wherein said CLDN6 comprises the amino acid sequence according to SEQ ID NO: 1 or a variant of said amino acid sequence.

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