Department of Pathobiology, University of Pennsylvania, Philadelphia, PA 19104, USA.
J Immunol. 2011 Jul 1;187(1):266-73. doi: 10.4049/jimmunol.1004182. Epub 2011 May 27.
IL-27 is a cytokine that regulates Th function during autoimmune and pathogen-induced immune responses. Although previous studies have shown that regulatory T cells (Tregs) express the IL-27R, and that IL-27 inhibits forkhead box P3 upregulation in vitro, little is known about how IL-27 influences Tregs in vivo. The studies presented in this article show that mice that overexpress IL-27 had decreased Treg frequencies and developed spontaneous inflammation. Although IL-27 did not cause mature Tregs to downregulate forkhead box P3, transgenic overexpression in vivo limited the size of a differentiating Treg population in a bone marrow chimera model, which correlated with reduced production of IL-2, a vital cytokine for Treg maintenance. These data identify an indirect role for IL-27 in shaping the Treg pool.
白细胞介素 27(IL-27)是一种细胞因子,可调节自身免疫和病原体诱导的免疫反应中的 Th 功能。尽管先前的研究表明调节性 T 细胞(Tregs)表达 IL-27R,并且 IL-27 可抑制体外叉头框 P3 的上调,但对于 IL-27 如何在体内影响 Tregs 知之甚少。本文介绍的研究表明,高表达 IL-27 的小鼠 Treg 频率降低,并发生自发性炎症。尽管 IL-27 不会导致成熟 Tregs 下调叉头框 P3,但体内转基因过表达限制了骨髓嵌合体模型中分化 Treg 群体的大小,这与 IL-2 的产生减少相关,IL-2 是 Treg 维持的重要细胞因子。这些数据确定了 IL-27 在塑造 Treg 库中的间接作用。