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Clonal Deletion Prunes but Does Not Eliminate Self-Specific αß CD8(+) T Lymphocytes.
Yu, Wong; Jiang, Ning; Ebert, Peter J R; Kidd, Brian A; Müller, Sabina; Lund, Peder J; Juang, Jeremy; Adachi, Keishi; Tse, Tiffany; Birnbaum, Michael E; Newell, Evan W; Wilson, Darrell M; Grotenbreg, Gijsbert M; Valitutti, Salvatore; Quake, Stephen R; Davis, Mark M.
Afiliação
  • Yu W; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA; Division of Hematology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Jiang N; Department of Bioengineering, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Ebert PJ; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Kidd BA; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Müller S; INSERM, UMR1043, Centre de Physiopathologie de Toulouse Purpan, Toulouse, France and Université Toulouse III Paul-Sabatier, 31024 Toulouse, France.
  • Lund PJ; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Juang J; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Adachi K; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Tse T; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Birnbaum ME; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Newell EW; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Wilson DM; Department of Pediatric Endocrinology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Grotenbreg GM; Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
  • Valitutti S; INSERM, UMR1043, Centre de Physiopathologie de Toulouse Purpan, Toulouse, France and Université Toulouse III Paul-Sabatier, 31024 Toulouse, France.
  • Quake SR; Department of Bioengineering, Stanford University School of Medicine, Stanford, CA 94305, USA; Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Davis MM; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA; Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address: mmdavis@stanford.edu.
Immunity ; 42(5): 929-41, 2015 May 19.
Article em En | MEDLINE | ID: mdl-25992863
ABSTRACT
It has long been thought that clonal deletion efficiently removes almost all self-specific T cells from the peripheral repertoire. We found that self-peptide MHC-specific CD8(+) T cells in the blood of healthy humans were present in frequencies similar to those specific for non-self antigens. For the Y chromosome-encoded SMCY antigen, self-specific T cells exhibited only a 3-fold lower average frequency in males versus females and were anergic with respect to peptide activation, although this inhibition could be overcome by a stronger stimulus. We conclude that clonal deletion prunes but does not eliminate self-specific T cells and suggest that to do so would create holes in the repertoire that pathogens could readily exploit. In support of this hypothesis, we detected T cells specific for all 20 amino acid variants at the p5 position of a hepatitis C virus epitope in a random group of blood donors.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deleção Clonal / Linfócitos T CD8-Positivos Limite: Animals / Female / Humans / Male Idioma: En Revista: Immunity Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deleção Clonal / Linfócitos T CD8-Positivos Limite: Animals / Female / Humans / Male Idioma: En Revista: Immunity Ano de publicação: 2015 Tipo de documento: Article