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. 1976 Aug 1;144(2):519-32.
doi: 10.1084/jem.144.2.519.

H-2 compatibility requirement for virus-specific T-cell-mediated cytolysis. Evaluation of the role of H-2I region and non-H-2 genes in regulating immune response

H-2 compatibility requirement for virus-specific T-cell-mediated cytolysis. Evaluation of the role of H-2I region and non-H-2 genes in regulating immune response

R M Zinkernagel et al. J Exp Med. .

Abstract

Lymphocytic choriomeningitis virus (LCMV) and ectromelia virus-specific T-cell-mediated cytotoxicity was assayed in various strain combinations using as targets peritoneal macrophages which have been shown to express Ia antigens. Virus-specific cytotoxicity was found only in H-2K- or D-region compatible combinations. I-region compatibility was not necessary nor alone sufficient for lysis. Six different I-region specificities had no obvious effect on the capacity to generate in vivo specific cytotoxicity (expressed in vitro) associated with Dd. Low LCMV-specific cytotoxic activity generated in DBA/2 mice was caused by the non-H-2 genetic background. This trait was inversely related to the infectious virus dose and recessive. Non-H-2 genes, possibly involved in controlling initial spread and multiplication of virus, seem to be, at least in the examples tested, more important in determining virus-specific cytotoxic T-cell activity in spleens than are Ir genes coded in H-2.

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References

    1. Nature. 1974 Apr 19;248(5450):701-2 - PubMed
    1. J Exp Med. 1974 Dec 1;140(6):1660-75 - PubMed
    1. J Immunol. 1974 Apr;112(4):1548-52 - PubMed
    1. Proc Natl Acad Sci U S A. 1974 Dec;71(12):5014-6 - PubMed
    1. Science. 1972 Jan 21;175(4019):273-9 - PubMed

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