Yamagata Tetsuya, Skepner Jill, Yang Jianfei
Tempero, GlaxoSmithKline, Cambridge, MA, 02139, USA.
Arch Immunol Ther Exp (Warsz). 2015 Dec;63(6):405-14. doi: 10.1007/s00005-015-0362-x. Epub 2015 Sep 10.
Interleukin (IL)-17-producing T cells, especially T helper (Th)17 cells, play a critical role in the pathogenesis of a variety of autoimmune inflammatory diseases. The pathogenic function of Th17 cells results from their production of Th17 effector cytokines, namely IL-17 (or IL-17A), IL-17F, IL-22 and IL-26. The importance of IL-17 has been demonstrated by antibody neutralization studies in both animal models of autoimmune diseases as well as in human clinical trials. This review highlights the current knowledge of the clinical aspects of the Th17 cytokines as well as therapeutic antibodies against IL-17, IL-17F, IL-17 receptor, IL-22, IL-26 and granulocyte macrophage colony-stimulating factor for the future treatment of autoimmune inflammatory diseases.
产生白细胞介素(IL)-17的T细胞,尤其是辅助性T(Th)17细胞,在多种自身免疫性炎症疾病的发病机制中起关键作用。Th17细胞的致病功能源于其产生的Th17效应细胞因子,即IL-17(或IL-17A)、IL-17F、IL-22和IL-26。在自身免疫性疾病动物模型以及人类临床试验中,抗体中和研究均证实了IL-17的重要性。本综述重点介绍了目前关于Th17细胞因子临床方面的知识,以及针对IL-17、IL-17F、IL-17受体、IL-22、IL-26和粒细胞巨噬细胞集落刺激因子的治疗性抗体,用于未来自身免疫性炎症疾病的治疗。