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. 1981 Mar 1;153(3):640-52.
doi: 10.1084/jem.153.3.640.

Hapten-specific T cell responses to 4-hydroxy-3-nitrophenyl acetyl. VII. Idiotype-specific suppression of plaque-forming cell responses

Hapten-specific T cell responses to 4-hydroxy-3-nitrophenyl acetyl. VII. Idiotype-specific suppression of plaque-forming cell responses

D H Sherr et al. J Exp Med. .

Abstract

The ability of suppressor cells induced by the intravenous administration of 4-hydro-3-nitrophenyl acetyl (NP)-modified syngeneic cells to reduce an idiotypic B cell response was studied in both an in vivo and an in vitro system. Idiotype-positive B cells were assayed by the ability of guinea pig anti-idiotypic antiserum to specifically inhibit idiotype-positive plaque formation. It was found that up to 57% of the PFC response in vivo and 100% of the PFC response in vitro was inhibitable with antiidiotypic antiserum. The expression of these idiotype-positive B cells could be suppressed by the transfer of spleen cells form mice treated 7 d previously with NP coupled syngeneic cels. T cells are both required and sufficient for the transfer of idiotype specific suppression. The induction of these idiotype-specific T suppressor cells directly with antigen suggests that recognition of unique determinants on cell surfaces is important for regulation of lymphoid cell interactions. The role of idiotype-specific suppressor cells in the network of lymphoid interactions is discussed.

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References

    1. J Exp Med. 1967 Sep 1;126(3):423-42 - PubMed
    1. Biochemistry. 1970 Feb 17;9(4):1023-30 - PubMed
    1. Science. 1972 Jul 14;177(4044):178-80 - PubMed
    1. Proc Natl Acad Sci U S A. 1972 Sep;69(9):2701-5 - PubMed
    1. J Exp Med. 1974 Dec 1;140(6):1498-510 - PubMed

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