Experimental Immunology, Immunology Frontier Research Center (IFReC-WPI), Osaka University, Osaka 565-0871, Japan.
Experimental Immunology, Immunology Frontier Research Center (IFReC-WPI), Osaka University, Osaka 565-0871, Japan. Department of Dermatology, Graduate School of Medicine, Osaka University, Osaka565-0871, Japan.
Science. 2014 Dec 19;346(6216):1536-40. doi: 10.1126/science.aaa1292.
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.
自身免疫耐受需要天然存在的调节性 T (Treg) 细胞。然而,它们如何稳定地控制自身免疫性 T 细胞仍然不清楚。在这里,我们表明 Treg 细胞可以使自身反应性的人类 CD8(+) T 细胞在体外失能(即在抗原再刺激时增殖减少和细胞因子产生减少),可能是通过控制抗原呈递细胞的共刺激功能。失能 T 细胞表型为幼稚,其 T 细胞受体对同源抗原的亲和力低于激活的 T 细胞,并且表达几种共抑制分子,包括细胞毒性 T 淋巴细胞相关抗原-4(CTLA-4)。使用这些标准,我们在健康个体中检测到针对自身免疫性疾病白癜风中靶向皮肤抗原的失能 T 细胞。总的来说,我们的结果表明,Treg 细胞介导的自身免疫性 T 细胞失能诱导对于维持自身耐受很重要。