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Phenotypic identification of specific and nonspecific suppressor T-cell populations involved in the in vivo response to alloantigen.

作者信息

Devens B H, Webb D R

机构信息

Department of Inflammation Biology and Immunology, Syntex Discovery Research, Division of Syntex (USA) Inc., Palo Alto, California 94303.

出版信息

Cell Immunol. 1995 Mar;161(1):1-7. doi: 10.1006/cimm.1995.1001.

Abstract

The monoclonal antibody 984.D4.6 (ma984) has been previously shown to recognize antigen-specific suppressor T-cells in an in vitro alloantigenic mixed-lymphocyte response system. In addition, an antiserum generated in rabbits to the N-terminal sequence of the nonspecific suppressor factor SIRS (soluble immune response suppressor) has been shown to block the suppressive activity of nonspecific, concanavalin A-activated suppressor cells. In the present studies we have used these antibodies to investigate the development of T-suppressor activity in mice immunized with alloantigen. These studies demonstrate the development of two populations of suppressor cells, one of which is antigen nonspecific and inhibitable with anti-SIRS and a second that is antigen-specific and sensitive to removal by lysis with ma984 plus complement. These populations of suppressor cells arise well after the peak of cytolytic T-cell activity in response to alloantigen indicating asynchrony in the development of the immune response to alloantigen.

摘要

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