Laboratory of Molecular Immunology and the Immunology Center, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892-1674.
Cold Spring Harb Perspect Biol. 2018 Sep 4;10(9):a028449. doi: 10.1101/cshperspect.a028449.
Interleukin (IL)-2, IL-4, IL-7, IL-9, IL-15, and IL-21 form a family of cytokines based on their sharing the common cytokine receptor γ chain (γc), which was originally discovered as the third receptor component of the IL-2 receptor, IL-2Rγ. The gene is located on the X chromosome and is mutated in humans with X-linked severe combined immunodeficiency (XSCID). The breadth of the defects in XSCID could not be explained solely by defects in IL-2 signaling, and it is now clear that γc is a shared receptor component of the six cytokines noted above, making XSCID a disease of defective cytokine signaling. Janus kinase (JAK)3 associates with γc, and -deficient SCID phenocopies XSCID, findings that served to stimulate the development of JAK3 inhibitors as immunosuppressants. γc family cytokines collectively control broad aspects of lymphocyte development, growth, differentiation, and survival, and these cytokines are clinically important, related to allergic and autoimmune diseases and cancer as well as immunodeficiency. In this review, we discuss the actions of these cytokines, their critical biological roles and signaling pathways, focusing mainly on JAK/STAT (signal transducers and activators of transcription) signaling, and how this information is now being used in clinical therapeutic efforts.
白细胞介素 (IL)-2、IL-4、IL-7、IL-9、IL-15 和 IL-21 基于其共同的细胞因子受体 γ 链 (γc) 形成细胞因子家族,γc 最初被发现为 IL-2 受体的第三个受体成分,即 IL-2Rγ。该基因位于 X 染色体上,并在 X 连锁严重联合免疫缺陷 (XSCID) 患者中发生突变。XSCID 的缺陷范围不能仅用 IL-2 信号的缺陷来解释,现在很清楚,γc 是上述六种细胞因子的共同受体成分,使 XSCID 成为一种细胞因子信号缺陷疾病。Janus 激酶 (JAK)3 与 γc 相关,而 -缺陷 SCID 与 XSCID 表型相同,这些发现促使开发 JAK3 抑制剂作为免疫抑制剂。γc 家族细胞因子共同控制淋巴细胞发育、生长、分化和存活的广泛方面,这些细胞因子在临床上很重要,与过敏和自身免疫性疾病以及癌症和免疫缺陷有关。在这篇综述中,我们讨论了这些细胞因子的作用、它们的关键生物学作用和信号通路,主要集中在 JAK/STAT(信号转导和转录激活因子)信号上,以及如何将这些信息用于临床治疗努力。