Chung Yeonseok, Chang Seon Hee, Martinez Gustavo J, Yang Xuexian O, Nurieva Roza, Kang Hong Soon, Ma Li, Watowich Stephanie S, Jetten Anton M, Tian Qiang, Dong Chen
Department of Immunology, M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Immunity. 2009 Apr 17;30(4):576-87. doi: 10.1016/j.immuni.2009.02.007. Epub 2009 Apr 9.
T helper (Th) 17 cells have been recently discovered in both mouse and human. Here we show that interleukin-1 (IL-1) signaling on T cells is critically required for the early programming of Th17 cell lineage and Th17 cell-mediated autoimmunity. IL-1 receptor1 expression in T cells, which was induced by IL-6, was necessary for the induction of experimental autoimmune encephalomyelitis and for early Th17 cell differentiation in vivo. Moreover, IL-1 signaling in T cells was required in dendritic cell-mediated Th17 cell differentiation from naive or regulatory precursors and IL-1 synergized with IL-6 and IL-23 to regulate Th17 cell differentiation and maintain cytokine expression in effector Th17 cells. Importantly, IL-1 regulated the expression of the transcription factors IRF4 and RORgammat during Th17 cell differentiation; overexpression of these two factors resulted in IL-1-independent Th17 cell polarization. Our data thus indicate a critical role of IL-1 in Th17 cell differentiation and this pathway may serve as a unique target for Th17 cell-mediated immunopathology.
辅助性T细胞17(Th17细胞)最近在小鼠和人类中均被发现。在此我们表明,T细胞上的白细胞介素-1(IL-1)信号传导对于Th17细胞谱系的早期编程以及Th17细胞介导的自身免疫至关重要。由IL-6诱导的T细胞中白细胞介素-1受体1(IL-1R1)的表达,对于实验性自身免疫性脑脊髓炎的诱导以及体内早期Th17细胞分化是必需的。此外,树突状细胞介导的从初始或调节性前体细胞向Th17细胞的分化需要T细胞中的IL-1信号传导,并且IL-1与IL-6和IL-23协同作用以调节Th17细胞分化并维持效应Th17细胞中的细胞因子表达。重要的是,IL-1在Th17细胞分化过程中调节转录因子IRF4和RORγt的表达;这两种因子的过表达导致不依赖IL-1的Th17细胞极化。因此,我们的数据表明IL-1在Th17细胞分化中起关键作用,并且该途径可能作为Th17细胞介导的免疫病理学的独特靶点。
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