Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2009 Jul;10(7):689-95.
doi: 10.1038/ni.1760.

Foxp3+ regulatory T cells: differentiation, specification, subphenotypes

Affiliations
Review

Foxp3+ regulatory T cells: differentiation, specification, subphenotypes

Markus Feuerer et al. Nat Immunol. 2009 Jul.

Abstract

Regulatory T cells (T(reg) cells) characterized by expression of the transcription factor Foxp3 play a key role in immune homeostasis. Rather than a monomorphic population strictly determined by Foxp3 as a 'master regulator', the emerging view is one of T(reg) cells as a population with many levels of complexity. Several regulatory factors partake in the control of their transcriptional 'signature', with Foxp3 being a key regulator but insufficient and unnecessary to specify all aspects of the lineage. Distinct subphenotypes of Foxp3+ T(reg) cells are found in different anatomical locations. Some subphenotypes specifically control different facets of effector T cell function and, perhaps surprisingly, share transcriptional control elements with the very cells they regulate. This review will focus on these novel aspects of T(reg) cell diversity.

PubMed Disclaimer

References

    1. J Immunol. 2005 Jul 1;175(1):246-53 - PubMed
    1. Nat Immunol. 2007 Sep;8(9):967-74 - PubMed
    1. J Immunol. 2007 Apr 1;178(7):4022-6 - PubMed
    1. Immunity. 2006 Sep;25(3):455-71 - PubMed
    1. Proc Natl Acad Sci U S A. 2004 Mar 30;101(13):4566-71 - PubMed

Publication types

MeSH terms

LinkOut - more resources