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Trends Immunol. 2015 Jun;36(6):344-53. doi: 10.1016/j.it.2015.04.006. Epub 2015 May 13.

Regulatory T cell identity: formation and maintenance.

Author information

1
Nomis Foundation Laboratories for Immunobiology and Microbial Pathogenesis, The Salk Institute for Biological Studies, 10010N. Torrey Pines Road, La Jolla, CA 92037, USA.
2
Nomis Foundation Laboratories for Immunobiology and Microbial Pathogenesis, The Salk Institute for Biological Studies, 10010N. Torrey Pines Road, La Jolla, CA 92037, USA. Electronic address: yzheng@salk.edu.

Abstract

T regulatory (Treg) cells are central to the maintenance of immune homeostasis. The transcription factor forkhead box P3 (Foxp3) is essential for specifying the Treg cell lineage during development, and continued expression of Foxp3 in mature Treg cells is necessary for suppressive function. Loss of Foxp3 expression in Treg cells is associated with autoimmune pathology. Here, we review recent insights into the mechanisms that maintain Treg cell stability and function, and place these findings within the broader understanding of mechanisms that establish Treg cell identity during development. We integrate emerging principles in Treg cell lineage maintenance with the mechanisms that allow Treg cells to sense and respond to varied inflammatory environments, and outline important areas of future inquiry in this context.

KEYWORDS:

CpG methylation; DNA looping; Foxp3; TCR; regulatory T cell

PMID:
25981968
PMCID:
PMC4458194
DOI:
10.1016/j.it.2015.04.006
[Indexed for MEDLINE]
Free PMC Article

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