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J Immunol. 2010 Jan 1;184(1):30-4. doi: 10.4049/jimmunol.0903412. Epub 2009 Nov 30.

Cutting edge: the Th1 response inhibits the generation of peripheral regulatory T cells.

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1
Department of Pathology, University of California, San Francisco, San Francisco, CA 94143-0511, USA.

Abstract

The possibility that effector T cells can be converted into forkhead box P3(+) regulatory T cells (Tregs) has potential therapeutic implications. To analyze the relationship between Th1 effectors and Tregs, we have used a model of systemic autoimmunity in which both effector and Tregs arise from a single population specific for a transgene-encoded systemic protein. In vitro, the presence of IFN-gamma inhibits Treg generation during activation. Using IFN-gamma reporter mice, we demonstrate that IFN-gamma-producing cells tend not to develop into Tregs, and Th1 priming of T cells prior to cell transfer limits the number of forkhead box P3(+) T cells generated in vivo. Moreover, transfer of IFN-gamma(-/-) or STAT1(-/-) T cells resulted in an increase in the number of Tregs. These data support a role for Th1 effector molecules and transcription factors in the control of peripheral Treg generation and demonstrates the limited plasticity of Th1 populations.

PMID:
19949064
PMCID:
PMC2908389
DOI:
10.4049/jimmunol.0903412
[Indexed for MEDLINE]
Free PMC Article
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