Cancerous Disease modifying antibodies

Abstract

The present invention relates to a method for producing cancerous disease modifying antibodies using a novel paradigm of screening. By segregating the anti-cancer antibodies using cancer cell cytotoxicity as an end point, the process makes possible the production of anti-cancer antibodies for therapeutic and diagnostic purposes. The antibodies can be used in aid of staging and diagnosis of a cancer, and can be used to treat primary tumors and tumor metastases. The anti-cancer antibodies can be conjugated to toxins, enzymes, radioactive compounds, cytokines, interferons, target or reporter moieties and hematogenous cells.

1 . A method for initiating antibody induced cytotoxicity of cancerous cells in a tissue sample selected from a human ovarian or colon tumor comprising:
 providing a tissue sample from said human ovarian or colon tumor;   providing the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04, the humanized antibody of the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04, the chimeric antibody of the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04, or antigen binding fragments thereof, which antigen binding fragments are characterized by an ability to competitively inhibit binding of said isolated monoclonal antibody to its target antigen; and   contacting said isolated monoclonal antibody, said humanized antibody, said chimeric antibody or said antigen binding fragments thereof with said tissue sample;   wherein binding of said isolated monoclonal antibody, said humanized antibody, said chimeric antibody or said antigen binding fragments thereof with said tissue sample induces cytotoxicity.   
   
   
       2 . A method of reduction of a human ovarian or colon tumor susceptible to antibody induced cytotoxicity in a mammal, wherein said human tumor expresses at least one epitope of an antigen which specifically binds to the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04 or an antigen binding fragment thereof, which antigen binding fragment is characterized by an ability to competitively inhibit binding of said isolated monoclonal antibody to its target antigen, comprising administering to said mammal said monoclonal antibody or said antigen binding fragment thereof in an amount effective to result in a reduction of said mammal's ovarian or colon tumor burden. 
   
   
       3 . The method of  claim 2  wherein said isolated monoclonal antibody or antigen binding fragment thereof is conjugated to a cytotoxic moiety. 
   
   
       4 . The method of  claim 3  wherein said cytotoxic moiety is a radioactive isotope. 
   
   
       5 . The method of  claim 2  wherein said isolated monoclonal antibody or antigen binding fragment thereof activates complement. 
   
   
       6 . The method of  claim 2  wherein said isolated monoclonal antibody or antigen binding fragment thereof mediates antibody dependent cellular cytotoxicity. 
   
   
       7 . The method of  claim 2  wherein said isolated monoclonal antibody is a humanized antibody of the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04 or an antigen binding fragment produced from said humanized antibody. 
   
   
       8 . The method of  claim 2  wherein said isolated monoclonal antibody is a chimeric antibody of the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04 or an antigen binding fragment produced from said chimeric antibody. 
   
   
       9 . A monoclonal antibody which specifically binds to the same epitope or epitopes as the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04. 
   
   
       10 . A method of reduction of a human ovarian or colon tumor in a mammal, wherein said human ovarian or colon tumor expresses at least one epitope of an antigen which specifically binds to the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04 or an antigen binding fragment thereof, which antigen binding fragment is characterized by an ability to competitively inhibit binding of said isolated monoclonal antibody to its target antigen, comprising administering to said mammal said monoclonal antibody or antigen binding fragment thereof in an amount effective to result in a reduction of said mammal's ovarian or colon tumor burden. 
   
   
       11 . The method of  claim 10  wherein said isolated monoclonal antibody or antigen binding fragment thereof is conjugated to a cytotoxic moiety. 
   
   
       12 . The method of  claim 11  wherein said cytotoxic moiety is a radioactive isotope. 
   
   
       13 . The method of  claim 10  wherein said isolated monoclonal antibody or antigen binding fragment thereof activates complement. 
   
   
       14 . The method of  claim 10  wherein said isolated monoclonal antibody or antigen binding fragment thereof mediates antibody dependent cellular cytotoxicity. 
   
   
       15 . The method of  claim 10  wherein said isolated monoclonal antibody is a humanized antibody of the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04 or an antigen binding fragment produced from said humanized antibody. 
   
   
       16 . The method of  claim 10  wherein said isolated monoclonal antibody is a chimeric antibody of the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04 or an antigen binding fragment produced from said chimeric antibody. 
   
   
       17 . A method of reduction of a human ovarian or colon tumor in a mammal, wherein said human ovarian or colon tumor expresses at least one epitope of an antigen which specifically binds to the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04 or an antigen binding fragment thereof, which antigen binding fragment is characterized by an ability to competitively inhibit binding of said isolated monoclonal antibody to its target antigen, comprising administering to said mammal said monoclonal antibody or antigen binding fragment thereof in conjunction with at least one chemotherapeutic agent in an amount effective to result in a reduction of said mammal's ovarian or colon tumor burden. 
   
   
       18 . The method of  claim 17  wherein said isolated monoclonal antibody or antigen binding fragment thereof is conjugated to a cytotoxic moiety. 
   
   
       19 . The method of  claim 18  wherein said cytotoxic moiety is a radioactive isotope. 
   
   
       20 . The method of  claim 17  wherein said isolated monoclonal antibody or antigen binding fragment thereof activates complement. 
   
   
       21 . The method of  claim 17  wherein said isolated monoclonal antibody or antigen binding fragment thereof mediates antibody dependent cellular cytotoxicity. 
   
   
       22 . The method of  claim 17  wherein said isolated monoclonal antibody is a humanized antibody of the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04 or an antigen binding fragment produced from said humanized antibody. 
   
   
       23 . The method of  claim 17  wherein said isolated monoclonal antibody is a chimeric antibody of the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04 or an antigen binding fragment produced from said chimeric antibody. 
   
   
       24 . A binding assay to determine a presence of cancerous cells in a tissue sample selected from a human ovarian or colon tumor, which is specifically bound by the isolated monoclonal antibody produced by hybridoma cell line AR53A10.11 having IDAC Accession No. 141205-04, the humanized antibody of the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04, the chimeric antibody of the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04, or antigen binding fragments thereof comprising:
 providing a tissue sample from said human tumor;   providing at least one of said isolated monoclonal antibody, said humanized antibody, said chimeric antibody or said antigen binding fragment thereof that recognizes the same epitope or epitopes as those recognized by the isolated monoclonal antibody produced by a hybridoma cell line AR53A10.11 having IDAC Accession No. 141205-04;   contacting at least one of said provided antibodies or antigen binding fragment thereof with said tissue sample; and   determining binding of said at least one provided antibody or antigen binding fragment thereof with said tissue sample;   whereby the presence of said cancerous cells in said tissue sample is indicated.   
   
   
       25 . Use of monoclonal antibodies for reduction of human ovarian or colon tumor burden, wherein said human ovarian or colon tumor expresses at least one epitope of an antigen which specifically binds to the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04 or an antigen binding fragment thereof, which antigen binding fragment is characterized by an ability to competitively inhibit binding of said isolated monoclonal antibody to its target antigen, comprising administering to said mammal said monoclonal antibody or antigen binding fragment thereof in an amount effective to result in a reduction of said mammal's human ovarian or colon tumor burden. 
   
   
       26 . The method of  claim 25  wherein said isolated monoclonal antibody or antigen binding fragment thereof is conjugated to a cytotoxic moiety. 
   
   
       27 . The method of  claim 26  wherein said cytotoxic moiety is a radioactive isotope. 
   
   
       28 . The method of  claim 25  wherein said isolated monoclonal antibody or antigen binding fragment thereof activates complement. 
   
   
       29 . The method of  claim 25  wherein said isolated monoclonal antibody or antigen binding fragment thereof mediates antibody dependent cellular cytotoxicity. 
   
   
       30 . The method of  claim 25  wherein said isolated monoclonal antibody is a humanized antibody of the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04 or an antigen binding fragment produced from said humanized antibody. 
   
   
       31 . The method of  claim 25  wherein said isolated monoclonal antibody is a chimeric antibody of the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04 or an antigen binding fragment produced from said chimeric antibody. 
   
   
       32 . Use of monoclonal antibodies for reduction of human ovarian or colon tumor burden, wherein said human ovarian or colon tumor expresses at least one epitope of an antigen which specifically binds to the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04 or an antigen binding fragment thereof, which antigen binding fragment is characterized by an ability to competitively inhibit binding of said isolated monoclonal antibody to its target antigen, comprising administering to said mammal said monoclonal antibody or antigen binding fragment thereof, in conjunction with at least one chemotherapeutic agent in an amount effective to result in a reduction of said mammal's human ovarian or colon tumor burden. 
   
   
       33 . The method of  claim 32  wherein said isolated monoclonal antibody or antigen binding fragment thereof is conjugated to a cytotoxic moiety. 
   
   
       34 . The method of  claim 33  wherein said cytotoxic moiety is a radioactive isotope. 
   
   
       35 . The method of  claim 32  wherein said isolated monoclonal antibody or antigen binding fragment thereof activates complement. 
   
   
       36 . The method of  claim 32  wherein said isolated monoclonal antibody or antigen binding fragment thereof mediates antibody dependent cellular cytotoxicity. 
   
   
       37 . The method of  claim 32  wherein said isolated monoclonal antibody is a humanized antibody of the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04 or an antigen binding fragment produced from said humanized antibody. 
   
   
       38 . The method of  claim 32  wherein said isolated monoclonal antibody is a chimeric antibody of the isolated monoclonal antibody produced by the hybridoma deposited with the IDAC as accession number 141205-04 or an antigen binding fragment produced from said chimeric antibody.