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PMID: 15785758 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

A well adapted regulatory contrivance: regulatory T cell development and the forkhead family transcription factor Foxp3.

Nature immunology ·Vol. 6 ·No. 4 ·2005-04-00 ·Pages 331-7

Fontenot JD, Rudensky AY

Abstract

The random generation of antigen receptors in developing lymphocytes results in a considerable risk of autoimmunity. Regulatory T cells (T(reg) cells) act in a dominant, trans-acting way to actively suppress immune activation and maintain immune tolerance. Here, we discuss the principal advances in our understanding of the molecular mechanisms of T(reg) cell development and function with particular emphasis on the forkhead transcription factor Foxp3. Accumulating evidence suggests that T(reg) cells represent a dedicated T cell lineage and that Foxp3 functions as the T(reg) cell lineage specification factor. The aggressive early-onset lymphoproliferative syndrome resulting from Foxp3 deficiency identifies T(reg) cells as vital mediators of immunological tolerance to self and Foxp3 as the mediator of the genetic mechanism of dominant tolerance.

MeSH Terms
Animals Antigens, CD/immunology DNA-Binding Proteins/immunology Forkhead Transcription Factors Humans Mice Receptors, Antigen, T-Cell/immunology Self Tolerance/immunology T-Lymphocytes/immunology Thymus Gland/immunology
Chemicals
Antigens, CD DNA-Binding Proteins FOXP3 protein, human Forkhead Transcription Factors Foxp3 protein, mouse Receptors, Antigen, T-Cell
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Fontenot Jason D
Department of Immunology, University of Washington School of Medicine, Seattle, Washington 98195, USA. [email protected]
Rudensky Alexander Y
Article Info
Journal
Nature immunology
Abbr.
Nat Immunol
ISSN
1529-2908
Published
2005-04-00
Pages
331-7
Language
English
Region
United States
NLM ID
100941354
Subset
IM
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