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. 1979 Apr 1;149(4):910-22.
doi: 10.1084/jem.149.4.910.

Idiotypic determinants on T-cell subpopulations

Idiotypic determinants on T-cell subpopulations

H Binz et al. J Exp Med. .

Abstract

Killer T cells with specificity for major histocompatibility antigens have been shown in mice and rats to display idiotypic receptors allowing the lysis of such cells at the effector phase by anti-idiotypic antibodies and complement. A comparison was made between idiotypes displayed by Lyt-1-2+3+ and Lyt-1+2-3- T blasts, generated in the same mixed leucocyte culture (MLC), across an entire H-2 locus barrier. This was done by absorption of anti-idiotypic antibodies with respective T blasts, followed by estimation of the ability of the absorbed antiserum to inhibit MLC or killer T-cell function. Further, the capacity of Lyt-purified, MLC-generated T blasts to provoke specific unresponsiveness via anti-idiotypic immunity in syngeneic recipients was analyzed. Taken together, the results demonstrate that Lyt-1+2-3- T blasts responsible for the major part of MLC proliferation have distincly different idiotypes from those on the Lyt 1-2+3+ killer T cells. That the idiotypes on the killer T-cell presursors can serve as triggering sites for induction of effector T-cell function was then suggested by experiments with Lyt-1-2+3+-purified, normal T cells as precursor cells in vitro. The fact that autoanti-idiotypic antibodies may circumvent the need for helper Lyt-1+2-3- T cells in the generation of allospecific killer T cells indicates that the former cells may normally function partly via such anti-idiotypic reactions.

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References

    1. Transplant Rev. 1975;22:175-95 - PubMed
    1. Nature. 1975 Dec 18;258(5536):614-6 - PubMed
    1. Nature. 1976 May 13;261(5556):139-41 - PubMed
    1. Nature. 1976 Jan 29;259(5541):273-81 - PubMed
    1. J Exp Med. 1976 Dec 1;144(6):1545-53 - PubMed

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