Monoclonal antibodies against tumor-associated antigens, processes for the preparation thereof and the use thereof

Abstract

The invention relates to monoclonal antibodies against a tumor-associated antigen which is mainly derived from tumors from the group of carcinomas of the breast, ovaries and prostate, as well as adenocarcinomas of the lung, which additionally react with polymorphic epithelial mucin (PEM), to the preparation and use thereof and to the use of the epitope defined by the antibody for diagnosis and therapy.

Description

The invention relates to monoclonal antibodies against a tumor-associated antigen which is mainly derived from tumors from the group of carcinomas of the breast, ovaries and prostate, as well as adenocarcinomas of the lung, which additionally react with polymorphic epithelial mucin (PEM), to the preparation and use thereof and to the use of the epitope defined by the antibody for diagnosis and therapy.

Hybridoma technology has made it possible to prepare specific monoclonal; antibodies (MAbs) even against unpurified antigens. This fact has made it possible to identify a large number of tumor-associated antigens (TAAs) which occur on certain human tumors but also on normal human tissues. Examples of such TAAs are CEA (carcinoembryonic antigen), N-CAM (neural cell adhesion molecule) and PEM (polymorphic epithelial mucin).

CEA is mainly expressed on adenocarcinomas of the gastro-intestinal tract, N-CAM is located on tumors derived from neuroectoderm, and PEM occurs mainly on carcinomas of the breast and ovaries. The TAAs which have just been mentioned are high molecular weight glycoproteins which carry a large number of immunogenic epitopes for the murine immune system. Comparative immunohistochemical investigations on cryopreserved human tissues demonstrate that the specificity of an MAb which recognizes with its idiotype (V region) an epitope I on a TAA may show a different tissue binding than an MAb which recognizes an epitope II (Buchegger et al. (1984), Int. J. Cancer 33: 643-649).

Multifarious reasons are possible for this observation: crypticity of epitopes in certain tissues, cross-reactive epitopes on different antigens, changes in conformation of antigens on secretion from tissues into the plasma (Bosslet et al. (1988), Eur. J. Nucl. Med. 14: 523-528) etc. It may be concluded from this that the specificity of an MAb is not unambiguously given by the definition of the recognized antigen but is given by the exact description of the V region of the MAb in conjunction with its immunohistochemical specificity for cryopreserved human tissues and its serum specificity with circulating TAA structures in human serum or plasma. Thus, for example, a number of MAbs against the PEM which was isolated by Shimizu from human milk, (Shimizu, M. and Yamauchi, K. (1982), J. Biochem. 91, 515-524) have been developed and bind to different epitopes and, accordingly, have different properties (Girling et al. (1989), 43, 1072-1076, Taylor-Papadimitriou et al. (1981), Int. J. Cancer, 28, 17-21).

Certain anti-PEM MAbs (EMFG 1,2) show a strong reaction with human carcinomas of the breast and ovaries but also react significantly with normal human tissues (Taylor-Papadimitriou et al. (1981)). Other MAbs (SM 3, Girling et al. (1989)) react more weakly and heterogeneously with carcinomas of the breast and ovaries but, on the other hand, do not bind significantly to normal human tissue.

We have succeeded, surprisingly, in producing an anti-PEM MAb which reacts strongly with carcinomas of the breast, ovaries and prostate, as well as adenocarcinomas of the lung, binds only weakly to normal human tissue and, in addition, is able to detect PEM very specifically in human serum or plasma. Methods for the immunochemical determination of antigen are known to the person skilled in the art (see Gosling (1990), Clin. Chem. 36/8, 1408-1427). In this connection a distinction is made essentially between two classes: homogeneous assays such as, for example, particle-enhanced nephelometry or turbidimetry and heterogeneous methods, also called solid-phase assays.

Solid-phase assays are designed so that the analyte antigen is immobilized out of the sample to be investigated by a trapping antibody bound to a solid phase, and the immobilized antigen is detected by a second antibody provided with a detectable labeling moiety (conjugate). Detectable labels of this type are known to the person skilled in the art, and examples are enzymes, chemiluminescent or electrochemiluminescent, radioactive or else colored labels.

The hybridoma cell line BW 835 which produces the monoclonal antibody BW 835 was deposited on Oct. 11, 1991, at DSM, Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH, Mascheroder Weg 1b, D-3300 Braunschweig, under the number DSM ACC2022.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1a is a nucleic acid sequence of BW 835 V.sub.H.

FIG. 1b is a nucleic acid sequence of BW 835 V.sub.K.

FIG. 2 shows the cloning of plasmic A which harbors a human IgG.sub.3 .DELTA.C gene in which the H1, H2 and H3 exons have been deleted. See Example 1.

FIG. 3 shows the cloning of plasmid B. See Example 2.

FIG. 4 shows the cloning of plasmid C. See Example 3.

FIG. 5 shows the cloning of plasmid D. See Example 4.

FIG. 6 shows the cloning of plasmid D to obtain plasmid E. See Example 5.

FIG. 7 shows the isolation of plasmid F. See Example 6.

FIG. 8 shows the cleavage of plasmid F to obtain plasmid G. See Example 7.

FIG. 9 shows the cleavage of plasmid E to obtain plasmid H. See Example 8.

FIG. 10 shows the partial cleavage of clone H to obtain plasmid I. See Example 9.

FIG. 11a shows the restriction cleavage sites for Mab BW 835 V.sub.H. See Example 10.

FIG. 11b shows the restriction cleavage sites for Mab BW 835 V.sub.K. See Example 10.

FIG. 12 shows the isolation of plasmids K1 and K2. See Example 10.

FIG. 13 shows the expression vector L1. See Example 11.

FIG. 14 shows the expression vector L2. See Example 11.

FIG. 15 compares the concentration of antigen bound by Mab BW 835 in serum or plasma of patients with malignant tumors with that in healthy patients. See Example 12.

FIG. 16 compares the concentration of tumor-associated antigens defined by Mab BW 835 in serum samples using peroxidase-labeled DF.sub.3, antibody conjugate together with Mab SW 835. See Example 13.

Antibodies within the meaning of this invention also mean antibody fragments.

The preparation and the properties of this MAb (BW 835) are described below:

The MAb was generated by immunizing Balb/c mice with the MCF-7 and SW-613 breast carcinoma cell lines by methods known from the literature (EP-A2-0 141079).

The distribution of the epitope defined by the MAb BW 835 on cryopreserved human carcinomas and normal human tissues is shown in Tables Ia and b respectively, comparing with the MAb SM-3 (Girling et al. 1989). The data are based on an immunohistochemical detection with the APAAP technique (Cordell at al. (1984), J. Histochem. Cytochem. 32, 219). It can clearly be seen that MAb BW 835 reacts strongly with all 15 carcinomas of the breast from 15 tested carcinomas of the breast, whereas the MAb SM-3 detects only 11 of 15 carcinomas of the breast.

In the case of carcinoma of the ovaries, the MAb BW 835 reacts strongly with 6 of 8 tested tumors, and the MAb SM-3 reacts with a few cells in 6 of 8 carcinomas. With all the other carcinoma types tested, especially the adenocarcinomas of the lung and the carcinomas of the prostate, MAb BW 835 shows a quantitatively stronger reaction. These data show that MAb BW 835 detect more carcinomas with a quantitatively stronger reaction than the MAb SM-3 disclosed in the literature.

The binding of MAb BW 835 to normal human tissue is shown in Table Ib. The APAAP technique was employed to obtain the data in this case too. The epitope defined by MAb BW 835 is expressed significantly on the ductal epithelium of the breast and the ductal epithelium of the pancreas, and is weakly expressed on the surface epithelium of the lungs, on some nerve fibers and on the collecting tubules and the glomeruli of the kidney. All the other tested normal tissues are negative.

Because of its high selectivity, the MAb BW 835 can also be used as inducer for internal image anti-paratope MAbs. MAbs of this type might be employed as epitope vaccine for the therapy of human tumors.

The demonstration that the epitope defined by the MAb BW 835 is located on the PEM defined by MAb SM-3 was checked by a double-determinant assay.

TABLE Ia__________________________________________________________________________Binding of the MAb BW 835 to cryopreserved human tumorsHuman tumor typeCarcinomas Ovarian Prostate Stomach Colon Pancreas Lung carcinomas of the breast carcinomas carcinomas carcinomas carcinomas carcinomas SCLC adeno Squamous Large cellMAb pos./total pos./total pos./total pos./total pos./total pos./total pos./total pos./total pos./total pos./total__________________________________________________________________________BW 835 15/15 6/8 4.degree./5 4*/6 3*/4 4*/7 4*/10 11.degree. /12 5*/11 7.degree./11SM 3 11/15 6*/8 1.degree./5 3*/6 1.degree./4 3.degree./7 2*/10 6*/12 4*/11 3*/11__________________________________________________________________________ *a few cells positive a few areas of secreted products positive TABLE Ib______________________________________Binding of the MAb BW 835 to cryopreserved normal human tissueTissue type:______________________________________Mammary glandPositive reaction with the acinar epithelium, positiveapical staining of the epithelium in the ducts and insome secreting vesiclesOvaryNegativePancreasPositive apical staining in the ductsLiverNegativeSpleenNegativeColonNegativeStomachMucosa and some mucin-containing ducts with positivereactionLungSurface epithelium of the lung with weak positive reactionKidneySome glomeruli weakly stained, positive apical stainingof the collecting tubulesBrainNegativePeripheral nerveSome nerve fibers weakly stainedBone marrowNegativePeripheral blood componentsLymphocytes, monocytes, granulocytes, erythrocytes,platelets are negative______________________________________

The MAb BW 835 used as trap was able to trap from cell culture supernatants of the T47 cell line an antigen which was detectable by the enzyme-labeled MAb SM-3. Furthermore, in the Western blot both MAbs stain molecules which correspond to the molecular weight position of PEM.

Once the immunological specificity data for the MAb BW 835 were defined, the mRNA was isolated from 10.sup.8 hybridoma cells which secrete the MAb BW 835, the V genes of the heavy and light chains of the MAb BW 835 were isolated by the method described by Orlandi et al. (1989), Proc. Natl. Acad. Sci. USA: 86, 3833-3837, and the nucleic acid sequence of the essential regions of the V gene exons were determined by the method described by Sanger et al. (1977), Proc. Natl. Acad. Sci., USA: 74, 5463-5467 (FIGS. 1a, b) (SEQ ID Nos. 1-4).

On repeated high-dose administration of MAbs of murine origin, such as, for example, the MAb BW 835, for in vivo therapy of humans it is possible to immunize the patients. They are able to produce human anti-mouse immunoglobulin antibodies (HAMA) after about 10-14 days (Miller et al., (1983), Blood, 62, 988; Joseph et al., (1988), European Journal of Nuclear Medicine, 14, 367). These HAMAs may have unfavorable effects on the pharmacokinetics and pharmacodynamics of the MAb and impede continuation of the treatment.

In order to reduce the immunogenicity of xenogenic antibodies as far as possible, a technique in which only the CDR loops of the V.sub.L and V.sub.H domains of the xenogenic antibodies are transferred to V.sub.L and V.sub.H domains of human antibodies has been developed (Jones, P. T., et al)., (1986), Nature, 321, 522) (EP-A-87302620, G. Winter), and this process is called "humanization" and takes place at the level of the V.sub.H and V.sub.L genes.

The technical procedure for humanization of an antibody is divided essentially into three sections: the cloning and nucleic acid sequence analysis of the specific V.sub.H and V.sub.L genes, the computer-assisted design of the synthetic oligonucleotides for the transfer of the CDR loops to the human V.sub.H and V.sub.L domains and the transfer of the CDR loops to human V.sub.H and V.sub.L domains by specific mutagenesis (Riechmann, L., et al., (1988), Nature, 332, 323; Verhoeyen, M., et al., (1988), Science, 239, 1534).

Humanization of this type can also be carried out on MAb BW 835 in order to improve its usability in vivo. This would entail the authentic CDR regions of the BW 835 V.sub.H and V.sub.L domains (defined by Kabat, E. A., et al. (1987) Sequences of Proteins of Immunological Interest, fourth edition, US Dept. of Health and Human Services, US Government Printing Office) or CDR regions with a few modified amino acids being transferred to human V.sub.H and V.sub.L domains, it being possible for a few amino acids of the framework regions located between the CDR regions to be taken over from the mouse antibody to the humanized antibody in order to minimise the change in the antigen-binding properties of the resulting MAb BW 835 in the humanized form.

The variable domains of the humMAb BW 835 are accordingly composed of the framework regions, which are authentic or modified at a few points, of the variable domains of a human MAb onto which the CDR regions which are authentic or have been modified at a few amino-acid positions of the mouse MAb BW 835 have been transplanted.

The following examples describe the steps necessary for cloning and nucleic acid sequence analysis of the V genes and for the expression of BW 835 specificity as chimeric MAb. The techniques used in Examples 1-12 were, unless otherwise indicated, taken from Molecular Cloning, a Laboratory Manual; Sambrook, Fritsch, Maniatis; Cold Spring Harbor Laboratory, 1982 (pages 11-44, 51-127, 133-134, 141, 146, 150-167, 170, 188-193, 197-199, 248-255, 270-294, 310-328, 364-401, 437-506) and from Molecular Cloning, A Laboratory Manual, Second Edition; Sambrook, Fritsch, Maniatis; Cold spring Harbor Laboratory Press, 1989 (pages 16.2-16.22, 16.30-16.40, 16.54-16.55).

EXAMPLE 1

The plasmid clone 54.1.24 which harbors the human IgG.sub.3 .DELTA.C gene (FIG. 2) (DE-A1-38 25 615, FIG. 2) was cleaved with PstI. The vector resulting from this was ligated to the largest of the resulting PstI insert fragments and transformed into bacteria. The plasmid clone A which harbors a human IgG.sub.3 .DELTA.C gene in which the H1, H2 and H3 exons have been deleted (IgG3.DELTA.) was identified by restriction analysis and nucleic acid sequence determination.

EXAMPLE 2

The plasmid clone A was cleaved with HindIII and EcoRI, the ends were filled in with Klenow polymerase, the IgG.sub.3 .DELTA. insert was isolated and ligated into a pUCl9 vector cleaved with SstI and provided with blunt ends with the aid of T.sub.4 polymerase. A plasmid clone B in which the IgG.sub.3 .DELTA. gene is orientated so that the HindIII cleavage site is located at the 5' end and the EcoRI cleavage site is located at the 3' end of the pUCl9 polylinker was identified by restriction mapping and nucleic acid sequence analysis (FIG. 3).

EXAMPLE 3

The plasmid clone B was cleaved with EcoRI and HindIII, the IgG.sub.3 .DELTA. insert was isolated and ligated into a KS+ plasmid vector (pBluescriptII KS+; Stratagene, La Jolla, Calif.) likewise cleaved with HindIII and EcoRI. The phasmid clone C in which the IgG3.DELTA. gene is flanked at the 5' and at the 3' end by a BamHI cleavage site was isolated (FIG. 4).

EXAMPLE 4

The phasmid clone C was cleaved with BamHI, the IgG3.alpha. insert was isolated and ligated into the expression vector pABStop (Wirth et al. (1988), Gene, 73, 419-426) likewise cleaved with BamHI. The expression plasmid D which contains the IgG.sub.3 .DELTA. C gene in the orientation shown in FIG. 5 was identified. In this cloning the pA3Stop vector loses the polyadenylation signal and SV40 stop located between the two BamHI cleavage sites.

EXAMPLE 5

The expression plasmid D was partially cleaved with BamHI, the ends were filled in with Klenow polymerase and religated. The expression plasmid E in which the BamHI cleavage site 3' from the IgG.sub.3 .DELTA. gene is destroyed was isolated (FIG. 6).

EXAMPLE 6

The human C kappa gene (Hieter et al. (1982), J. Biol. Chem., 257, No. 3, 1516-1522) was obtained as EcoRI fragment cloned in pBR 322 from Prof. P. Leder, Harvard Medical School. The pBR322 vector was cleaved with EcoRI, the EcoRI cleavage sites were filled in, the C kappa insert was isolated and ligated into a pUCl9 vector cleaved with SmaI. The plasmid clone F in which the C kappa gene is flanked at the 5' end by a HindIII after a BamHI cleavage site and at the 3' end by an EcoRI cleavage site was isolated (FIG. 7).

EXAMPLE 7

The plasmid clone F was cleaved with HindIII and EcoRI, the C kappa insert was isolated and cloned into a HindIII/EcoRI-cleaved KS+ phasmid. The phasmid clone G in which the C kappa insert is flanked at the 5' and at the 3' end by a BamHI cleavage site was isolated (FIG. 8).

EXAMPLE 8

The phasmid clone G was cleaved with BamHI, the C kappa insert was isolated and cloned into a pAB stop vector cleaved with BamHI. The clone H in which the C kappa gene is orientated so that the HindIII cleavage site of the pAB stop vector is located at its 5' end was identified by restriction mapping and nucleic acid sequence analysis (FIG. 9).

EXAMPLE 9

The clone E was partially cleaved with BamHI, the restriction ends were filled in and religated. The clone I in which the BamHI cleavage site 3' of the C kappa gene is destroyed was identified by restriction mapping (FIG. 10).

EXAMPLE 10

The V.sub.H and V.sub.K genes of the MAb BW 835 were amplified using the PCR technique and specific oligonucleotides by the method of Orlandi et al. (1989) and cloned in KS+ vectors (Gussow and Seemann (1991), Methods in Enzymology, Vol. 203) which contained V.sub.H and V.sub.K genes with suitable restriction cleavage sites (FIG. 11 a for V.sub.H amd b for V.sub.K). The clones K1 and K2 which contain the V.sub.H (K1) and V.sub.K (K2) genes of the MAb BW 835 were isolated (FIG. 12).

EXAMPLE 11

The nucleic acid sequences of the V.sub.H and V.sub.X genes of the MAb BW 835 from the clones K1 and K2 were determined by the method of Sanger et al. (1977) (FIGS. 1a, b) (SEQ ID Nos. 1-4). It is possible to generate mimetics based on the CDRs from this sequence by the method described by Saragovi et al. (Saragovi et al. (1991), Science 253, 792-795).

Furthermore, the V.sub.B and V.sub.K gene inserts were cut out of the clones K1 and K2 with the aid of the restriction endonucleases HindIII and BamHI and were cloned into the vectors D (V.sub.H) and I (V.sub.K) likewise cleaved with HindIII and BamHI. The expression vectors L1 and L2 which contain immunoglobulin heavy (L1) (FIG. 13) and light (L2) (FIG. 14) chain genes with the V genes of MAb BW 835 were isolated. The expression vectors L1 and L2 can be used for the expression of a chimeric MAb with the specificity of MAb BW 835.

Examples 12 and 13 are intended to explain the use of the MAb BW 835 for serodiagnosis of malignant tumors.

EXAMPLE 12

The MAb BW 835 was bound by adsorption to the walls of wells of microtiter plates (NUNC) by methods known to the person skilled in the art (Tijssen, P., "Practice and theory of enzyme immunoassay" Elsevier (1988), 297-328). 10 .mu.l of sample were pipetted into each of the wells prepared in this way and each containing 100 .mu.l of buffer (OSND, Behringwerke) and incubated at +37.degree. C. for 2 hours. After washing three times with diluted Enzygnost washing buffer (OSEW, Behringwerke), 100 .mu.l of MAb BW 835 (1 .mu.g/ml) which was conjugated to peroxidase by known methods were introduced into each of the individual wells. The following 2-hour incubation step at +37.degree. C. was completed by a cycle of three washes. Subsequently, for the third incubation step at room temperature, 100 .mu.l of a buffer/substrate chromogen solution (OUVG/OUVF, Behringwerke) were pipetted into each of the wells, and the enzyme reaction was stopped after 30 minutes with 100 .mu.l of Enzygnost stop solution (OSFA, Behringwerke). The extinction of the samples was determined as 450 nm.

Result:

The extinctions determined in this way correspond in the level thereof to the concentration of the antigen in the sample. The concentration of the antigen defined by the specific binding of MAb BW 835 in serum or plasma of patients with malignant tumors is distinctly raised by comparison with that in healthy patients (FIG. 15). In FIG. 15, NS means normal sera and Mamma I-IV indicates the different degrees of development of mamma-carcinoma. The broken line in the Figure is the cut-off value, which is defined as the 90th percentile of a group of normal sera. This particularly applies to patients with late-stage carcinoma of the breast, but also, surprisingly, to those with early-stage carcinoma who, with other commercial tumor marker tests for detecting breast cancer-associated antigens in serum (for example CA 15-3), by comparison give false-negative findings significantly more often, and thus overall better sensitivities were found for the homologous version described.

EXAMPLE 13

It is also possible to use for the detection of PEM in serum in the double-determinant assay in combination with the MAb BW 835 other peroxidase-labeled antibodies which recognize further epitopes on the tumor-associated antigens defined by MAb BW 835. To do this, for example, a test analogous to Example 12 was carried out using the DF3 antibody disclosed in the literature (Kufe et al. (1984), Hybridoma 3, 223) in peroxidase-labeled form (CA 15-3-Test, Boehringer Mannheim) as conjugate component.

Result:

The use of, for example, DF3-POD as conjugate component to supplement the solid-phase-bound BW 835 produced distinctly higher serum values for the tumor sera compared with a normal serum pool and patients with benign diseases, which once again underlines the potential of the MAb BW 835 as specific component for a tumor marker test (FIG. 16).

__________________________________________________________________________# SEQUENCE LISTING- (1) GENERAL INFORMATION:- (iii) NUMBER OF SEQUENCES: 4- (2) INFORMATION FOR SEQ ID NO:1:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 115 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:- Leu Gln Ser Leu Arg Ala Leu Val Gln Pro Gl - #y Gly Ser Met Lys Leu# 15- Ser Cys Val Ala Ser Gly Phe Thr Phe Ser As - #n Tyr Trp Met Asn Trp# 30- Val Arg Gln Ser Pro Glu Lys Gly Leu Glu Tr - #p Val Ala Glu Ile Arg# 45- Leu Lys Ser Asn Asn Tyr Ala Thr His Tyr Al - #a Glu Ser Val Lys Gly# 60- Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Se - #r Ser Val Tyr Leu Gln#805- Met Asn Asn Leu Arg Ala Glu Asp Thr Gly Il - #e Tyr Tyr Cys Ile Arg# 95- Glu Thr Val Phe Tyr Tyr Tyr Ala Met Asp Ty - #r Trp Gly Gln Gly Thr# 110- Thr Val Thr 115- (2) INFORMATION FOR SEQ ID NO:2:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 345 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: DNA (genomic)- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:- CTGCAGAGTC TGAGAGCCTT GGTGCAACCT GGAGGATCCA TGAAACTCTC CT - #GTGTTGCC 60- TCTGGATTCA CTTTCAGTAA CTACTGGATG AACTGGGTCC GCCAGTCTCC AG - #AGAAGGGG 120- CTTGAGTGGG TTGCTGAAAT TAGATTGAAA TCTAATAATT ATGCAACACA TT - #ATGCGGAG 180- TCTGTGAAAG GGAGGTTCAC CATCTCAAGA GATGATTCCA AAAGTAGTGT CT - #ACCTGCAA 240- ATGAACAACT TAAGAGCTGA AGACACTGGC ATTTATTACT GTATCAGGGA GA - #CGGTTTTT 300# 345TA CTGGGGCCAA GGGACCACGG TCACC- (2) INFORMATION FOR SEQ ID NO:3:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 108 amino (B) TYPE: amino acid (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:3:- Gln Leu Thr Gln Ser Pro Pro Ser Val Pro Va - #l Thr Pro Gly Glu Ser# 15- Val Ser Ile Ser Cys Arg Ser Ser Gln Ser Le - #u Leu His Gly Asp Gly# 30- Asn Thr Tyr Leu Tyr Trp Phe Leu Gln Arg Pr - #o Gly Gln Ser Pro Arg# 45- Leu Leu Ile Tyr Arg Met Ser Asn Leu Ala Se - #r Gly Val Pro Asp Arg# 60- Phe Ser Gly Ser Gly Ser Gly Thr Ala Phe Th - #r Leu Arg Ile Ser Arg#80- Val Glu Ala Glu Asp Val Gly Val Tyr Tyr Cy - #s Met Gln His Leu Glu# 95- Tyr Pro Phe Thr Phe Gly Gly Gly Lys Val Gl - #u Ile# 105- (2) INFORMATION FOR SEQ ID NO:4:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 325 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: DNA (genomic)- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:4:- CAGCTGACCC AGTCTCCACC CTCTGTACCT GTCACTCCTG GAGAGTCAGT AT - #CCATCTCC 60- TGCAGGTCTA GTCAGAGTCT CCTGCATGGT GATGGCAACA CTTACTTGTA TT - #GGTTCCTG 120- CAGAGGCCAG GCCAGTCTCC TCGGCTCCTG ATATATCGGA TGTCCAACCT TG - #CCTCAGGA 180- GTCCCAGACA GGTTCAGTGG CAGTGGGTCA GGAACTGCTT TCACACTGAG AA - #TCAGTAGA 240- GTGGAGGCTG AGGATGTGGG TGTTTATTAC TGTATGCAAC ATCTAGAATA TC - #CTTTCACG 300# 325 TGGA GATCA__________________________________________________________________________

Claims

1. An isolated antibody or antigen-binding fragment thereof having binding affinity for a tumor-associated antigen, wherein the antigen is derived from a carcinoma of the breast, ovaries, prostate, stomach, colon, or pancreas, or adenocarcinoma of the lung, and wherein the antibody binds to polymorphic epithelial mucin (PEM) and binds to the same epitope as monoclonal antibody BW 835, DSM ACC2022.

2. A modified antibody that comprises the CDR regions of the variable domains of BW 835 represented by SEQ ID No: 1 and SEQ ID No: 3, wherein the CDR regions are grafted onto a human framework and wherein said modified antibody binds to the same epitope as monoclonal antibody BW 835, DSM ACC2022.

3. A method of detecting in vitro a tumor-associated antigen using an antibody or antigen binding fragment thereof according to claim 2.

4. The method of claim 3, wherein the antigen is derived from a carcinoma of the breast, ovaries, prostate, stomach, colon, or pancreas, or adenocarcinoma of the lung.

5. The method of claim 3, wherein the antigen is derived from breast carcinoma.