Department of Microbial Infection and Immunity, The Ohio State University College of Medicine and Wexner Medical Center, Columbus, OH 43210; and.
Biomedical Sciences Graduate Program, The Ohio State University College of Medicine and Wexner Medical Center, Columbus, OH 43210.
J Immunol. 2020 Oct 1;205(7):1721-1730. doi: 10.4049/jimmunol.2000612.
CD4 Th cells are responsible for orchestrating diverse, pathogen-specific immune responses through their differentiation into a number of subsets, including T1, T2, T9, T follicular helper, T follicular regulatory, and regulatory T cells. The differentiation of each subset is guided by distinct regulatory requirements, including those derived from extracellular cytokine signals. IL-2 has emerged as a critical immunomodulatory cytokine that both positively and negatively affects the differentiation of individual Th cell subsets. IL-2 signals are propagated, in part, via activation of STAT5, which functions as a key regulator of CD4 T cell gene programs. In this review, we discuss current understanding of the mechanisms that allow IL-2-STAT5 signaling to exert divergent effects across CD4 T cell subsets and highlight specific roles for this pathway in the regulation of individual Th cell differentiation programs.
CD4 T 细胞通过分化为多个亚群,包括 T1、T2、T9、滤泡辅助 T 细胞、滤泡调节 T 细胞和调节性 T 细胞,负责协调多种病原体特异性免疫反应。每个亚群的分化都受到不同的调节要求的指导,包括来自细胞外细胞因子信号的调节要求。IL-2 已成为一种关键的免疫调节细胞因子,它对单个 Th 细胞亚群的分化既有积极影响,也有消极影响。IL-2 信号的传递部分是通过激活 STAT5 实现的,STAT5 作为 CD4 T 细胞基因程序的关键调节剂发挥作用。在这篇综述中,我们讨论了目前对允许 IL-2-STAT5 信号在 CD4 T 细胞亚群中发挥不同作用的机制的理解,并强调了该途径在调节单个 Th 细胞分化程序中的特定作用。