The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
Trends Immunol. 2013 Feb;34(2):74-80. doi: 10.1016/j.it.2012.11.002. Epub 2012 Dec 6.
Regulatory T (Treg) cells are essential for immunological tolerance and homeostasis. Although forkhead box (Fox)p3 is continually required to reinforce the Treg cell program, Treg cells can also undergo stimulus-specific differentiation that is regulated by transcription factors typically associated with the differentiation of conventional CD4(+) T cells. This results in effector Treg (eTreg) cells with unique migratory and functional properties matched to the stimulus that elicited the initial response. Despite this functional and transcriptional heterogeneity, expression of the transcription factor B lymphocyte-induced maturation protein (Blimp)-1, a key player in late B cell and conventional T cell differentiation, is common to all eTreg cells. Here, we discuss the factors that control the differentiation of eTreg cells and their importance in disease settings.
调节性 T(Treg)细胞对于免疫耐受和稳态至关重要。虽然叉头框(Fox)p3 持续需要加强 Treg 细胞的程序,但 Treg 细胞也可以经历刺激特异性分化,其由通常与常规 CD4(+)T 细胞分化相关的转录因子调控。这导致效应性 Treg(eTreg)细胞具有与引发初始反应的刺激相匹配的独特迁移和功能特性。尽管存在功能和转录异质性,但转录因子 B 细胞诱导成熟蛋白(Blimp)-1 的表达是所有 eTreg 细胞共有的,Blimp-1 是晚期 B 细胞和常规 T 细胞分化中的关键因子。在这里,我们讨论控制 eTreg 细胞分化的因素及其在疾病环境中的重要性。