ANTI-GUCY2C ANTIBODIES AND USES THEREOF
The present invention is directed to antibodies that specifically bind to GUCY2c and methods of using such antibodies in the diagnosis and/or treatment of cancer.
1 . An isolated antibody that specifically binds to Guanylyl cyclase C (GUCY2c) and comprises:
a heavy chain variable region (VH) comprising a VH complementarity determining region one (CDR1), VH CDR2, and VH CDR3 of the amino acid sequence shown in SEQ ID NO: 2.
a light chain variable region (VL) comprising a VL CDR1, VL CDR2, and VL CDR3 of the amino acid sequence shown in SEQ ID NO: 1.
2 . The isolated antibody of claim 1 , wherein the antibody comprises a VH CDR1 comprising the amino acid sequence of SEQ ID NO: 6, a VH CDR2 comprising the amino acid sequence of SEQ ID NO: 7, a VH CDR3 comprising the amino acid sequence shown in SEQ ID NO: 8, a VL CDR1 comprising the amino acid sequence shown in SEQ ID NO: 3, a VL CDR2 comprising the amino acid sequence shown in SEQ ID NO: 4 and a VL CDR3 comprising the amino acid sequence shown in SEQ ID NO: 5.
3 . The isolated antibody of claim 1 , wherein the antibody comprises a VH comprising the amino acid sequence shown in SEQ ID NO: 2, or a variant thereof with one or several conservative amino acid substitutions in residues that are not within a CDR.
4 . The isolated antibody of claim 3 , wherein the antibody comprises a VL comprising the amino acid sequence shown in SEQ ID NO: 1, or a variant thereof with one or several amino acid substitutions in amino acids that are not within a CDR.
5 . The isolated antibody of claim 2 , wherein the antibody comprises a VH comprising the amino acid sequence shown in SEQ ID NO: 2, and a VL comprising the amino acid sequence shown in SEQ ID NO: 1.
6 . The isolated antibody of claim 2 , wherein the antibody comprises a heavy chain comprising the amino acid sequence shown in SEQ ID NO: 9, 10, 12 or 13 and a light chain comprising the amino acid sequence shown in SEQ ID NO: 11, 14, 15, 16, 17, 18, or 19.
7 . The isolated antibody of claim 6 , wherein the antibody comprises a heavy chain comprising the amino acid sequence shown in SEQ ID NO: 9 or 10 and a light chain comprising the amino acid sequence shown in SEQ ID NO: 11.
8 . The isolated antibody of claim 6 , wherein the antibody comprises a heavy chain comprising the amino acid sequence shown in SEQ ID NO: 12 or 13 and a light chain comprising the amino acid sequence shown in SEQ ID NO: 14, 15, 16, 17, 18, or 19.
9 . The isolated antibody of claim 2 , wherein the antibody comprises a constant region.
10 . The isolated antibody of claim 9 , wherein the antibody has an isotype that is selected from the group consisting of mouse IgG 1 or rabbit IgG.
11 . The isolated antibody of claim 9 , wherein the antibody is a rabbit chimeric antibody or a rabbitized antibody.
12 . (canceled)
13 . The isolated antibody of claim 2 , wherein the antibody specifically binds to human and cynomolgus monkey GUCY2c.
14 . The isolated antibody of claim 13 , wherein the antibody does not bind to mouse GUCY2c.
15 . The isolated antibody of claim 2 , wherein the antibody binds to cytoplasmic GUCY2c.
16 . An isolated cell line that produces the antibody of claim 2 .
17 . An isolated nucleic acid encoding the antibody of claim 2 .
18 . A recombinant expression vector comprising the nucleic acid of claim 17 .
19 . A host cell comprising the expression vector of claim 18 .
20 . A hybridoma capable of producing the antibody of claim 2 .
21 . (canceled)
22 . (canceled)
23 . (canceled)
24 . (canceled)
25 . A composition comprising the antibody of claim 2 , and a carrier.
26 . A kit for the diagnosis of cancer comprising the composition of claim 25 .
27 . A method for diagnosing cancer in a subject, the method comprising contacting a test sample of tissue cells suspected of containing cancerous tumor cells obtained from the subject with the antibody of claim 2 .
28 . The method of claim 27 , further comprising detecting the formation of a complex between the antibody and GUCY2c in the sample, and classifying a higher level of formation of such a complex in the test sample as compared to the level of formation of such a complex in a control sample of normal tissue cells from the same type of tissue as the sample, as diagnostic of the presence of cancer in the subject.
29 . The method of claim 27 , wherein the cancer is selected from the group consisting of colorectal cancer, gastric cancer, sarcoma, lymphoma, Hodgkin's lymphoma, leukemia, head and neck cancer, squamous cell head and neck cancer, thymic cancer, epithelial cancer, salivary cancer, liver cancer, stomach cancer, thyroid cancer, lung cancer, ovarian cancer, breast cancer, prostate cancer, esophageal cancer, pancreatic cancer, glioma, leukemia, multiple myeloma, renal cell carcinoma, bladder cancer, cervical cancer, choriocarcinoma, colon cancer, oral cancer, skin cancer, and melanoma.
30 . The method of claim 27 , wherein the antibody is detectably labeled.
31 . A method of diagnosing the presence of cancer in a subject, the method comprising
determining the level of expression of Guanylyl cyclase C (GUCY2c) in
a test sample of tissue cells obtained from tissue suspected of containing cancerous tumor cells in the subject and
a control sample of known normal cells obtained from the same type of tissue as the test sample,
wherein determining the level of expression of GUCY2c comprises employing an antibody of claim 2 , and
classifying a higher level of expression of GUCY2c in the test sample as compared to the control sample, as diagnostic of the presence of cancer in the subject from which the test sample was obtained.
32 . The method of claim 31 , wherein the step employing the antibody comprises an immunohistochemistry or Western blot analysis.