CD4 + Regulatory T Cells Control T H 17 Responses in a Stat3-Dependent Manner

Author:

Chaudhry Ashutosh12,Rudra Dipayan12,Treuting Piper3,Samstein Robert M.1,Liang Yuqiong1,Kas Arnold2,Rudensky Alexander Y.12

Affiliation:

1. Howard Hughes Medical Institute and Immunology Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.

2. Department of Immunology, University of Washington, Seattle, WA 98195, USA.

3. Department of Comparative Medicine, University of Washington, Seattle, WA 98195, USA.

Abstract

Outfoxing Immune Excess Immune responses are kept in check by Foxp3-expressing CD4 + -regulatory T cells (T regs ) through a variety of mechanisms. Expression of specific transcription factors directs T reg responses into distinct T helper cell lineages; however, the transcription factors that regulate particular helper lineages have not been completely characterized. Chaudhry et al. (p. 986 , published online 1 October) show that the transcription factor Stat3, that is required for the initial differentiation of T H 17-effector T cells, is also required for T reg cell-mediated suppression of T H 17-mediated immune responses. Mice carrying a T reg cellspecific deletion in Stat3 succumb to an intestinal inflammatory disease driven by uncontrolled T H 17 responses. Thus, different classes of immune responses can result from the expression of helper lineage–specific transcription factors.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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