The long-term objective of these studies is to define selected antigens of human cells using antibodies produced in non-human primates. The immunological perspective of the non-human primates should allow the recognition of epitopes on these antigens which may be difficult to be detected by lower mammalian species.
The specific aims for this renewal period are to: (1) establish the optimal conditions and method for production of chimpanzee monoclonal antibodies to selected human normal and malignant cell antigens; (2) establish the optimal conditions and methods for the in vitro transfection or infection of chimpanzee cells with oncogenes or human tumor DNA; and (3) from aim 2, establish the immunogenicity of tumorigenicity of chimpanzee cells that show evidence of gene insertion or changes in vitro growth characteristics. Specifically, aim 1 will evaluate various methods of chimpanzee B-cell fusion such as electrofusion and PEG, varying the conditions for fusion and growth as well as the parental human and murine myeloma lines to be used as fusion partners. In particular, aim 2 will evaluate various in vitro methods of gene insertion including transfection and infection of chimpanzee fibroblast, epithelial cells, or lymphocytes.
Aim 3 will utilize standard injection and serological procedures adapted in this laboratory to induce and measure the autologous immune response in chimpanzees to human gene insertion, their in vitro growth properties, and the nature of the insertion technique. (CS)

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA040044-24
Application #
3179479
Study Section
Immunobiology Study Section (IMB)
Project Start
1975-05-01
Project End
1990-04-30
Budget Start
1987-05-01
Budget End
1988-04-30
Support Year
24
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Duke University
Department
Type
Schools of Medicine
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
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Kim, Y W; Kern, H F; Mullins, T D et al. (1989) Characterization of clones of a human pancreatic adenocarcinoma cell line representing different stages of differentiation. Pancreas 4:353-62
Zeleznik-Le, N J; Metzgar, R S (1989) Expression of CD9 antigen on normal activated human B cells. Cell Immunol 123:70-82
Haviland, A E; Borowitz, M J; Lan, M S et al. (1988) Aberrant expression of monoclonal antibody-defined colonic mucosal antigens in inflammatory bowel disease. Gastroenterology 95:1302-11
Lan, M S; Khorrami, A; Kaufman, B et al. (1987) Molecular characterization of a mucin-type antigen associated with human pancreatic cancer. The DU-PAN-2 antigen. J Biol Chem 262:12863-70