Department of Life Science, Sogang University, 35 Baekbeom-ro, Mapo-gu, Seoul 04107, Korea.
Int J Mol Sci. 2018 Mar 3;19(3):730. doi: 10.3390/ijms19030730.
T helper type 17 (Th17) cells and pTreg cells, which share a common precursor cell (the naïve CD4 T cell), require a common tumor growth factor (TGF)-β signal for initial differentiation. However, terminally differentiated cells fulfill opposite functions: Th17 cells cause autoimmunity and inflammation, whereas Treg cells inhibit these phenomena and maintain immune homeostasis. Thus, unraveling the mechanisms that affect the Th17/Treg cell balance is critical if we are to better understand autoimmunity and tolerance. Recent studies have identified many factors that influence this balance; these factors range from signaling pathways triggered by T cell receptors, costimulatory receptors, and cytokines, to various metabolic pathways and the intestinal microbiota. This review article summarizes recent advances in our understanding of the Th17/Treg balance and its implications with respect to autoimmune disease.
辅助性 T 细胞 17(Th17)细胞和 pTreg 细胞,它们具有共同的前体细胞(幼稚 CD4 T 细胞),需要共同的肿瘤生长因子(TGF)-β信号来进行初始分化。然而,终末分化的细胞发挥相反的功能:Th17 细胞引起自身免疫和炎症,而 Treg 细胞抑制这些现象并维持免疫稳态。因此,如果我们要更好地理解自身免疫和耐受,那么阐明影响 Th17/Treg 细胞平衡的机制是至关重要的。最近的研究已经确定了许多影响这种平衡的因素;这些因素包括 T 细胞受体、共刺激受体和细胞因子触发的信号通路,以及各种代谢途径和肠道微生物群。本文综述了我们对 Th17/Treg 平衡及其对自身免疫性疾病影响的理解的最新进展。