Monoclonal antibodies and monoclonal antibody fragments will be labeled with the beta-emitting radionuclide, yttrium-90 (90Y, T 1/2 = 64.- hr), and studied preclinically to assess their potential as agents for radioimmuntherapy of cancer. Bifunctional chelate techniques which will give enhanced in vivo stability will be developed in order to circumvent the high bone and reticuloendothelial uptakes and consequent dose-limiting bone marrow toxicity associated with currently available methods for production of 90Y-labeled monoclonal antibodies. Monoclonal antibody CO17-1A, which has specificity for colorectal and pancreatic carcinomas, will be chelate conjugated using the new bifunctional chelate techniques. Radioimmunoassay will be used to monitor retention of immunoreactivity following conjugation. Tissue distribution studies of 90Y-labeled CO17-1A in athymic nude mice bearing xenografts of human colorectal carcinoma cell line SW 948 will permit assessment of the potential of the new bifunctional chelate techniques. Control studies will be used to evaluate the importance of nonspecific binding. Absorbed radiation dose calculations will enable selection of tumoricidal dosages of 90Y-labeled CO17-1A for use in tumor growth/regression studies in nude mice bearing tumor xenografts. Calcium DTPA encapsulated in large unilamella vesicle (LUV) liposomes will be evaluated for decorporation of the 90Y which becomes dissociated in vivo from 90Y-labeled CO17-1A via either catabolism or """"""""leakage."""""""" Use of the radioprotective drug, WR- 2721, as an adjunct to 90Y-labeled monoclonal antibody therapy for reducing the radiation dose to the bone marrow will be studied. WR-2721 will also be coupled to monoconal antibody 16B-13, which has specificity for the bone marrow, in order to direct the radioprotective effect more specifically to that organ. The research will be extended to other monoclonal antibodies against gastrointestinal tumors (BR55-2 and 1116-NS-19-9) and melanoma (ME-361 and 691-19-19), as well as Fab and F(ab')2 fragments of monoclonal antibodies. This multidiscplinary research approach, which combines the fields of bio-organic chemistry, immunochemistry, and radiopharmacology, is aimed at development of improved methods for radioimmunotherapy of cancer in man.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
2R01CA039706-04
Application #
3179052
Study Section
Radiation Study Section (RAD)
Project Start
1985-09-01
Project End
1991-08-31
Budget Start
1988-09-01
Budget End
1989-08-31
Support Year
4
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Oak Ridge Associated Universities
Department
Type
DUNS #
City
Oak Ridge
State
TN
Country
United States
Zip Code
37831
Washburn, L C; Sun, T T; Lee, Y C et al. (1991) Comparison of five bifunctional chelate techniques for 90Y-labeled monoclonal antibody CO17-1A. Int J Rad Appl Instrum B 18:313-21
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