| Literature DB >> 25525252 |
Yuka Maeda1, Hiroyoshi Nishikawa2, Daisuke Sugiyama1, Danbee Ha1, Masahide Hamaguchi1, Takuro Saito1, Megumi Nishioka3, James B Wing1, Dennis Adeegbe1, Ichiro Katayama4, Shimon Sakaguchi2.
Abstract
Immunological tolerance to self requires naturally occurring regulatory T (Treg) cells. Yet how they stably control autoimmune T cells remains obscure. Here, we show that Treg cells can render self-reactive human CD8(+) T cells anergic (i.e., hypoproliferative and cytokine hypoproducing upon antigen restimulation) in vitro, likely by controlling the costimulatory function of antigen-presenting cells. Anergic T cells were naïve in phenotype, lower than activated T cells in T cell receptor affinity for cognate antigen, and expressed several coinhibitory molecules, including cytotoxic T lymphocyte-associated antigen-4 (CTLA-4). Using these criteria, we detected in healthy individuals anergic T cells reactive with a skin antigen targeted in the autoimmune disease vitiligo. Collectively, our results suggest that Treg cell-mediated induction of anergy in autoimmune T cells is important for maintaining self-tolerance.Entities:
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Year: 2014 PMID: 25525252 DOI: 10.1126/science.aaa1292
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728