FOXP3型
关贸总协定3
生物
效应器
免疫学
白细胞介素2受体
转录因子
STAT6
细胞生物学
免疫系统
T辅助细胞
Treg细胞
细胞分化
状态4
T细胞
白细胞介素4
信号转导
遗传学
基因
车站3
斯达
作者
Svetlana P. Chapoval,Preeta Dasgupta,Nicolas Dorsey,Achsah Keegan
摘要
Abstract Review discusses the regulation of Th2 cells by Tregs and vice versa and focuses on the interplay between the IL-4-activated STAT6/GATA3 pathway and Foxp3. During the development of immune responses to pathogens, self-antigens, or environmental allergens, naive CD4+ T cells differentiate into subsets of effector cells including Th1, Th2, and Th17 cells. The differentiation into these subsets is controlled by specific transcription factors. The activity of these effector cells is limited by nTregs and iTregs, whose differentiation and maintenance are dependent on the transcription factor Foxp3. The regulation of autoimmune diseases mediated by Th1 and Th17 cells by Tregs has been studied and reviewed extensively. However, much less has been presented about the interplay between Tregs and Th2 cells and their contribution to allergic disease. In this perspective, we discuss the regulation of Th2 cells by Tregs and vice versa, focusing on the interplay between the IL-4-activated STAT6/GATA3 pathway and Foxp3.
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