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- W71609746 abstract "Abstract Thymic negative selection renders the developing T-cell repertoire tolerant to self-major histocompatability complex (MHC)/peptide ligands. The major mechanism of induction of self-tolerance is thought to be thymic clonal deletion, ie, the induction of apoptotic cell death in thymocytes expressing a self-reactive T-cell receptor. Consistent with this hypothesis, in mice deficient in thymic clonal deletion mediated by cells of hematopoietic origin, a twofold to threefold increased generation of mature thymocytes has been observed. Here we describe the analysis of the specificity of T lymphocytes developing in the absence of clonal deletion mediated by hematopoietic cells. In vitro, targets expressing syngeneic MHC were readily lysed by activated CD8+ T cells from deletion-deficient mice. However, proliferative responses of T cells from these mice on activation with syngeneic antigen presenting cells were rather poor. In vivo, deletion-deficient T cells were incapable of induction of lethal graft-versus-host disease in syngeneic hosts. These data indicate that in the absence of thymic deletion mediated by hematopoietic cells functional T-cell tolerance can be induced by nonhematopoietic cells in the thymus. Moreover, our results emphasize the redundancy in thymic negative selection mechanisms." @default.
- W71609746 created "2016-06-24" @default.
- W71609746 creator A5027201117 @default.
- W71609746 creator A5072568067 @default.
- W71609746 date "1999-06-01" @default.
- W71609746 modified "2023-09-28" @default.
- W71609746 title "In Vivo T-Lymphocyte Tolerance in the Absence of Thymic Clonal Deletion Mediated by Hematopoietic Cells" @default.
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- W71609746 doi "https://doi.org/10.1182/blood.v93.11.3856" @default.
- W71609746 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/10339493" @default.
- W71609746 hasPublicationYear "1999" @default.
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