Science · 2014 · 206 citations · 23 references
Life SciencesCell BiologyImmunologyAutoimmunityCellular ImmunologyImmunoregulationAutoimmune DiseasesCell-mediated ImmunityRegulatory T CellsT Cell BiologyT Cell ToleranceTolerance MechanismsAntigen Presenting CellsCoinhibitory ReceptorsCytotoxic T Lymphocyte Antigen 4Cytotoxic T-lymphocyte Antigen 4 (Ctla-4) PathwayPeripheral Tolerance MechanismsReceptor Affinity RegulationT-cell Mediated AutoimmunityT-cell Regulation
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.
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