| Literature DB >> 25992863 |
Wong Yu1, Ning Jiang2, Peter J R Ebert3, Brian A Kidd3, Sabina Müller4, Peder J Lund3, Jeremy Juang3, Keishi Adachi3, Tiffany Tse3, Michael E Birnbaum3, Evan W Newell3, Darrell M Wilson5, Gijsbert M Grotenbreg6, Salvatore Valitutti4, Stephen R Quake7, Mark M Davis8.
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.Entities:
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Year: 2015 PMID: 25992863 PMCID: PMC4455602 DOI: 10.1016/j.immuni.2015.05.001
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745