New twists of T cell fate: control of T cell activation and tolerance by TGF-beta and NFAT.

Abstract:

:Protective and pathogenic immune responses were initially thought to be determined by the differentiation of naïve T cells into Th1 and Th2 effector subsets and the immunosuppressive activity of thymic-derived regulatory T cells. It is now clear that naïve T cells can also differentiate into 'induced' regulatory T cells or inflammatory T cells that secrete IL-17. These divergent T-cell subsets have opposing functions in imparting inflammation or tolerance, yet both developmental programs are controlled by the pluripotent cytokine transforming growth factor beta and the transcription factor NFAT. Recent findings have begun to shed light on the mechanisms by which TGF-beta and NFAT integrate multiple signaling inputs to determine the direction of naïve T-cell differentiation.

journal_name

Curr Opin Immunol

authors

Sundrud MS,Rao A

doi

10.1016/j.coi.2007.04.014

subject

Has Abstract

pub_date

2007-06-01 00:00:00

pages

287-93

issue

3

eissn

0952-7915

issn

1879-0372

pii

S0952-7915(07)00066-0

journal_volume

19

pub_type

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