4.6 Review

Differentiation and function of Foxp3+ effector regulatory T cells

期刊

TRENDS IN IMMUNOLOGY
卷 34, 期 2, 页码 74-80

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.it.2012.11.002

关键词

regulatory T cell; transcription; B lymphocyte-induced maturation protein-1; interleukin-10; differentiation; autoimmune disease

资金

  1. National Health and Medical Research Council (NHMRC) of Australia
  2. Australian Research Council

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据