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A syngeneic anti tumor serum recognizing a complex H-2 alloantigen.
Immunobiology
|August 1, 1979
Summary
BALB/c mice tumors showed high spontaneous regression rates. Antibodies generated against these tumors recognized antigens similar to foreign H-2 alloantigens, suggesting cross-reactivity.
Area of Science:
- Immunology
- Oncology
- Transplantation Immunology
Background:
- Methylcholanthrene-induced tumors in BALB/c mice (H-2d) exhibit spontaneous regression upon transplantation into syngeneic hosts.
- This regression phenomenon is associated with the development of iso-antibodies possessing significant anti-tumor cytotoxic activity.
Purpose of the Study:
- To analyze the specificity of antibodies generated against a regressing methylcholanthrene-induced tumor (MCG4) in BALB/c mice.
- To investigate the relationship between tumor-associated antigens and host alloantigens, particularly H-2 antigens.
Main Methods:
- Induction and transplantation of a methylcholanthrene-induced tumor in BALB/c mice.
- Generation of iso-antibodies from BALB/c mice bearing the tumor.
- Specificity analysis of anti-tumor antibodies using cytotoxicity assays against tumor cells and various mouse strains, including B10.W congenic strains with wild-derived H-2wi haplotypes.
Main Results:
- BALB/c anti-MCG4 sera exhibited high anti-tumor cytotoxic activity.
- Antibody specificity analysis revealed reactivity against a tumor antigen closely resembling H-2 alloantigens, such as H-2.5, found on normal cells of foreign mouse strains.
- The sera cross-reacted with nine out of ten B10.W congenic strains carrying H-2wi haplotypes derived from wild mice.
Conclusions:
- The study identified a tumor antigen on a regressing BALB/c tumor that shares similarities with foreign H-2 alloantigens.
- The findings suggest a potential cross-reactivity between tumor-specific antigens and allogeneic histocompatibility antigens.
- Further investigation is required to determine if the tumor antigen is identical to or merely cross-reactive with foreign H-2 antigens.