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The differentiation of suppressor cell populations as revealed by studies of the effects of mitogens on the mixed lymphocyte reaction and on the generation of cytotoxic lymphocytes.
Authors:K Ozato  J D Ebert  W H Adler
Institution:1. Department of Embryology, Carnegie Institution of Washington, 115 W. University Parkway, Baltimore, Maryland 21224 U.S.A.;2. Marine Biological Laboratory, Woods Hole, Massachusetts, U.S.A.;3. Laboratory of Cellular and Comparative Physiology, Gerontology Research Center, NICHD, PHS, U. S. Department of Health, Education and Welfare, Baltimore City Hospitals, Baltimore, Maryland 21224 U.S.A.
Abstract:The regulation by concanavalin A (Con A) and bacterial lipoloysaccharide (LPS) of the mixed lymphocyte reaction (MLR) and of the generation of cytotoxic lymphocytes (CL) was studied in congenic resistant mice using cortisone resistant thymocytes as the responding cells. LPS enhances the generation of CL selectively when suboptimal numbers of allogeneic cells are present in mixed lymphocyte cultures and also results in the augmentation of the MLR. Mitogenic concentrations of Con A on the other hand suppress the generation of CL regardless of alloantigen dose. The mechanism of suppression cannot be ascribed to the presence of suppressor T cells, since the addition to the cultures of syngeneic cortisone resistant thymocytes activated by Con A does not change the immune response. However, prospective suppressor cells that can be activated by Con A are located in secondary lymphoid organs such as spleen and lymph node. Suppressor activity by those cells is abolished by anti θ plus complement. Con A activated spleen cells suppress the MLR, whereas Con A activated thymocytes amplify the proliferation of responding cells.
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