Resistance to 402AX teratocarcinoma involves immunity to minor histocompatibility antigens
- 1 January 1987
- journal article
- research article
- Published by Springer Nature in Immunogenetics
- Vol. 26 (1-2) , 1-5
- https://doi.org/10.1007/bf00345447
Abstract
The 402AX teratocarcinoma is a 12/J-derived mouse major histocompatibility complex (MHC) antigen negative tumor that is induced to express H-2b class I antigens during rejection. Resistance to 402AX by MHC allogeneic and syngeneic mice is immunologically mediated and involves the recognition of tumor-associated antigens (TAA) in the context of induced MHC class I antigens. The current studies were undertaken to define the 402AX TAAs. Reconstitution of irradiated susceptible hosts (129/J) with 402AX-primed resistant spleen cells (C57BL/6) results in acute graft-versus-host disease, suggesting that tumor-primed C57BL/6 splenocytes are reactive to tumor genotype (129/J) minor histocompatibility (Hm) antigens. C57BL/6 anti-129/J effector cells, although not directly cytotoxic for 402AX cells, are specifically cold target inhibited by 402AX cells. Genetically susceptible hosts (C3H.SW) immunized to 129/J Hm antigens by skin grafting become resistant to an i.p. challenge of 402AX cells. These results suggest that 129/J Hm antigens may be the TAAs recognized during genetically controlled rejection of the 402AX teratocarcinoma.This publication has 23 references indexed in Scilit:
- H-2 class I antigen expression on mouse teratocarcinoma cell linesImmunogenetics, 1985
- Mice coisogenically immunized against H-2 class I antigens on transfected l cells reject transplanted embryonal carcinoma cellsImmunogenetics, 1985
- Regulation of major histocompatibility gene expression in teratocarcinoma 402AX cellsCell Differentiation, 1984
- Absence of significant H–2 and β2-microglobulin mRNA expression by mouse embryonal carcinoma cellsNature, 1982
- Susceptibility of allogeneic mice to teratocarcinoma 402AXImmunogenetics, 1980
- Teratocarcinoma transplantation rejection loci: AnH-2-linked tumor rejection locusImmunogenetics, 1979
- The genetics of teratocarcinoma transplantation: tumor formation in allogeneic hosts by the embryonal carcinoma cell lines F9 and PCC3Immunogenetics, 1978
- H–2 gene expression is required for T cell-mediated lysis of virus-infected target cellsNature, 1977
- H-2 compatibility is required for T-cell-mediated lysis of target cells infected with lymphocytic choriomeningitis virus.The Journal of Experimental Medicine, 1975
- ABSENCE OF SEROLOGICALLY DETECTABLE H-2 ON PRIMITIVE TERATOCARCINOMA CELLS IN CULTURETransplantation, 1974