Id2 and Id3 maintain the regulatory T cell pool to suppress inflammatory disease.

Abstract:

:Regulatory T (Treg) cells suppress the development of inflammatory disease, but our knowledge of transcriptional regulators that control this function remains incomplete. Here we show that expression of Id2 and Id3 in Treg cells was required to suppress development of fatal inflammatory disease. We found that T cell antigen receptor (TCR)-driven signaling initially decreased the abundance of Id3, which led to the activation of a follicular regulatory T (TFR) cell-specific transcription signature. However, sustained lower abundance of Id2 and Id3 interfered with proper development of TFR cells. Depletion of Id2 and Id3 expression in Treg cells resulted in compromised maintenance and localization of the Treg cell population. Thus, Id2 and Id3 enforce TFR cell checkpoints and control the maintenance and homing of Treg cells.

journal_name

Nat Immunol

journal_title

Nature immunology

authors

Miyazaki M,Miyazaki K,Chen S,Itoi M,Miller M,Lu LF,Varki N,Chang AN,Broide DH,Murre C

doi

10.1038/ni.2928

subject

Has Abstract

pub_date

2014-08-01 00:00:00

pages

767-76

issue

8

eissn

1529-2908

issn

1529-2916

pii

ni.2928

journal_volume

15

pub_type

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