Chin Robert K, Lo James C, Kim Oliver, Blink Sarah E, Christiansen Peter A, Peterson Pärt, Wang Yang, Ware Carl, Fu Yang-Xin
Department of Pathology and Committee in Immunology, The University of Chicago, Chicago, Illinois 60637, USA.
Nat Immunol. 2003 Nov;4(11):1121-7. doi: 10.1038/ni982. Epub 2003 Sep 28.
The autoimmune regulator Aire is a key mediator of central tolerance for peripherally restricted antigens. Its absence in human patients results in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy. The cellular signals that regulate Aire expression are undefined. We show here that lymphotoxin signaling is necessary for the expression of Aire and its downstream target genes. The failure of Aire induction in the thymi of lymphotoxin-deficient and lymphotoxin-beta receptor-deficient mice contributes to overt autoimmunity against self antigens normally protected by Aire. Conversely, stimulation of lymphotoxin-beta receptor by agonistic antibody leads to increased expression of Aire and tissue-restricted antigens in both intact thymi and cultured thymic epithelial cell line. These findings define the essential cross-talk between thymocytes and thymic stroma that is required for central tolerance.
自身免疫调节因子Aire是外周受限抗原中枢耐受的关键介质。人类患者缺乏该因子会导致自身免疫性多内分泌腺病-念珠菌病-外胚层发育不良。调节Aire表达的细胞信号尚不清楚。我们在此表明,淋巴毒素信号传导是Aire及其下游靶基因表达所必需的。淋巴毒素缺陷和淋巴毒素β受体缺陷小鼠胸腺中Aire诱导失败导致针对通常由Aire保护的自身抗原的明显自身免疫。相反,激动性抗体刺激淋巴毒素β受体可导致完整胸腺和培养的胸腺上皮细胞系中Aire和组织限制性抗原表达增加。这些发现定义了中枢耐受所需的胸腺细胞与胸腺基质之间的重要相互作用。