Control of regulatory T cell lineage commitment and maintenance.

TitleControl of regulatory T cell lineage commitment and maintenance.
Publication TypeJournal Article
Year of Publication2009
AuthorsJosefowicz SZ, Rudensky A
JournalImmunity
Volume30
Issue5
Pagination616-25
Date Published2009 May
ISSN1097-4180
KeywordsAnimals, Cell Differentiation, Cell Lineage, Cytokines, Forkhead Transcription Factors, Humans, Protein Kinases, Receptors, Antigen, T-Cell, T-Lymphocyte Subsets, T-Lymphocytes, Regulatory, Thymus Gland
Abstract

Foxp3-expressing regulatory T (Treg) cells suppress pathology mediated by immune responses against self and foreign antigens and commensal microorganisms. Sustained expression of the transcription factor Foxp3, a key distinguishing feature of Treg cells, is required for their differentiation and suppressor function. In addition, Foxp3 expression prevents deviation of Treg cells into effector T cell lineages and confers dependence of Treg cell survival and expansion on growth factors, foremost interleukin-2, provided by activated effector T cells. In this review we discuss Treg cell differentiation and maintenance with a particular emphasis on molecular regulation of Foxp3 expression, arguably a key to mechanistic understanding of biology of regulatory T cells.

DOI10.1016/j.immuni.2009.04.009
Alternate JournalImmunity
PubMed ID19464984
PubMed Central IDPMC4410181
Grant ListR01 AI061816 / AI / NIAID NIH HHS / United States
AI061816 / AI / NIAID NIH HHS / United States
Related Faculty: 
Steven Josefowicz, Ph.D.

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