Tianjin Key Laboratory of Retinal Functions and Diseases, Eye Institute and School of Optometry, Tianjin Medical University Eye Hospital, Tianjin 300384, China.
J Immunol Res. 2021 Mar 16;2021:6693542. doi: 10.1155/2021/6693542. eCollection 2021.
Increasing evidence has suggested that T helper 17 (Th17) cells play a central role in the pathogenesis of ocular immune disease. The association between pathogenic Th17 cells and the development of uveitis has been confirmed in experimental and clinical studies. Several cytokines affect the initiation and stabilization of the differentiation of Th17 cells. Therefore, understanding the mechanism of related cytokines in the differentiation of Th17 cells is important for exploring the pathogenesis and the potential therapeutic targets of uveitis. This article briefly describes the structures, mechanisms, and targeted drugs of cytokines-including interleukin (IL)-6, transforming growth factor-1 (TGF-1), IL-1, IL-23, IL-27, IL-35, IL-2, IL-4, IL-21, and interferon (IFN)--which have an important influence on the differentiation of Th17 cells and discusses their potential as therapeutic targets for treating autoimmune uveitis.
越来越多的证据表明辅助性 T 细胞 17(Th17)在眼免疫疾病的发病机制中发挥着核心作用。在实验和临床研究中已经证实致病性 Th17 细胞与葡萄膜炎的发生有关。几种细胞因子影响 Th17 细胞分化的起始和稳定。因此,了解相关细胞因子在 Th17 细胞分化中的作用机制对于探讨葡萄膜炎的发病机制和潜在的治疗靶点非常重要。本文简要描述了细胞因子——包括白细胞介素(IL)-6、转化生长因子-β1(TGF-β1)、IL-1、IL-23、IL-27、IL-35、IL-2、IL-4、IL-21 和干扰素(IFN)——在 Th17 细胞分化中的重要影响,并讨论了它们作为治疗自身免疫性葡萄膜炎的潜在治疗靶点的可能性。