Department of Immunology, The Forsyth Institute, 245 First Street, Cambridge, MA 02142, USA.
J Autoimmun. 2013 Feb;40:28-44. doi: 10.1016/j.jaut.2012.07.009. Epub 2012 Aug 24.
Compared with its pro-inflammatory function, the mechanisms underlying the anti-inflammatory effect of IL-6 are poorly understood. IL-6 can cooperate with TGF-β to induce IL-10 production in Th17 cells in vitro. However, the effect of IL-6 on generation of Tr1 cells and the in vivo importance of this effect are mostly uncharacterized. In this study, we showed that in vitro, IL-6 can induce the generation of IL-10-producing Tr1 cells from naïve CD4 T cells, independently of IL-27 and TGF-β. IL-6 induces IL-21 production in CD4 T cells and IL-10-inducing effect of IL-6 requires both IL-21 and IL-2. Although IL-6 cannot induce IL-10 production in CD8 T cells in a cell-autonomous manner, it can do so indirectly through promoting CD4 T cell IL-21 production. The IL-10-producing T cells induced by IL-6 have phenotypic, genetic and functional traits of Tr1 cells and can suppress LPS-induced in vivo inflammatory response in an IL-10-dependent fashion. Blockade of IL-6 in two autoimmune inflammation models, induced respectively by anti-CD3 antibody or Treg-depletion, led to reduction in IL-10-producing T cells and exacerbated inflammation of lung and intestine. Thus, we delineated critical pathways involved in IL-6-induced generation of Tr1 cells and demonstrated the importance of this event in restraining autoimmune tissue inflammation.
与促炎功能相比,IL-6 的抗炎作用机制尚未完全阐明。IL-6 可以与 TGF-β 协同作用,在体外诱导 Th17 细胞产生 IL-10。然而,IL-6 对 Tr1 细胞生成的影响及其在体内的重要性在很大程度上尚未得到描述。在这项研究中,我们表明,在体外,IL-6 可以独立于 IL-27 和 TGF-β 诱导幼稚 CD4 T 细胞产生产生 IL-10 的 Tr1 细胞。IL-6 诱导 CD4 T 细胞产生 IL-21,而 IL-6 诱导 IL-10 的作用需要 IL-21 和 IL-2。尽管 IL-6 不能以细胞自主性方式诱导 CD8 T 细胞产生 IL-10,但它可以通过促进 CD4 T 细胞 IL-21 产生来间接诱导。IL-6 诱导的产生 IL-10 的 T 细胞具有 Tr1 细胞的表型、遗传和功能特征,可通过依赖 IL-10 的方式抑制 LPS 诱导的体内炎症反应。在两种自身免疫炎症模型中阻断 IL-6(分别通过抗 CD3 抗体或 Treg 耗竭诱导)导致产生 IL-10 的 T 细胞减少,并加剧肺和肠的炎症。因此,我们描绘了 IL-6 诱导 Tr1 细胞生成的关键途径,并证明了这一事件在抑制自身免疫性组织炎症中的重要性。