Monoclonal antibodies and monoclonal antibody fragments with high specificities for human malignancies will be covalently coupled to DTPA via the cyclic DTPA anhydride technique to provide a means for labeling such agents with polyvalent metal radionuclides. The potential of radioimmunotherapy using monoclonal antibodies labeled with the alpha-emitting radionuclide fermium-255, (T1/2 = 20.1 h) and beta-emitting yttrium-90, T1/2 = 64.2 h) will be studied preclinically. Two gastrointestinal monoclonal antibodies with specificity for both colorectal and pancreatic carcinomas, 1083-17-1A (17-1A) and 1116-NS-19-9 (19-9), and a monoclonal antimelanoma antibody, 691-19-19 (19-19), will be investigated. Antibodies derivatized via the bifunctional chelate technique will be tested by a radioimmunoassay technique to verify their retention of immunological activity. Nude mice bearing the appropriate tumor type for each monoclonal antibody will be used to test the specificity of tumor uptake. Antibodies labeled with the gamma-emitting radionuclides indium-111, ytterbium-169, and yttrium-88 will be used for scintigraphic and tissue distribution studies to determine the time course of the tumor uptake of radiolabeled monoclonal antitumor antibodies. A radiolabeled monoclonal anti-influenza antibody will be used to control for nonspecific binding. The antibodies will then be labeled with Fm-255 and Y-90 as well as einsteinium-253 (a longer lived alpha emitter to be used as a model for Fm-255), and further tissue distribution studies will be carried out. These tissue distribution studies will be used for radiation dosimetry calculations. In vivo tumor growth studies in nude mice will be carried out to aid in assessment of the therapeutic potential of Fm255- and Y90-labeled monoclonal antibody derivatives. This multidisciplinary research approach, which combines the fields of bio-organic chemistry, immunochemistry, and radiopharmacology, is aimed at improving radioimmunotherapy methods for malignant processes in man.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA039706-02
Application #
3179054
Study Section
Radiation Study Section (RAD)
Project Start
1985-09-01
Project End
1988-08-31
Budget Start
1986-09-01
Budget End
1987-08-31
Support Year
2
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Oak Ridge Associated Universities
Department
Type
DUNS #
City
Oak Ridge
State
TN
Country
United States
Zip Code
37831
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Lee, Y C; Washburn, L C; Sun, T T et al. (1990) Radioimmunotherapy of human colorectal carcinoma xenografts using 90Y-labeled monoclonal antibody CO17-1A prepared by two bifunctional chelate techniques. Cancer Res 50:4546-51
Lee, Y C; Lawless, D; Crook, J E et al. (1989) Analysis of T lymphocyte subsets in tamarins with colitis and colon cancer. Am J Med Sci 297:118-22
Lawless, B D; Lee, Y C; Fuhr, J E et al. (1988) Colon cancer cells in peripheral blood of cancerous tamarins. Clin Immunol Immunopathol 48:338-42
Washburn, L C; Lee, Y C; Sun, T T et al. (1988) Preclinical assessment of 90Y-labeled monoclonal antibody CO17-1A, a potential agent for radioimmunotherapy of colorectal carcinoma. Int J Rad Appl Instrum B 15:707-11