Abstract:
:Recent work has identified a new subset of effector T cells that produces interleukin (IL)-17 known as T helper 17 (Th17) cells, which is involved in the pathophysiology of inflammatory diseases and is thought to be developmentally related to regulatory T (Treg) cells. Because of its importance for Treg cells, we examined the role of IL-2 in Th17 generation and demonstrate that a previously unrecognized aspect of IL-2 function is to constrain IL-17 production. Genetic deletion or antibody blockade of IL-2 promoted differentiation of the Th17 cell subset. Whereas STAT3 appeared to be a key positive regulator of RORgammat and IL-17 expression, absence of IL-2 or disruption of its signaling by deletion of the transcription factor STAT5 resulted in enhanced Th17 cell development. We conclude that in addition to the promotion of activation-induced cell death of lymphocytes and the generation of Treg cells, inhibition of Th17 polarization appears to be an important function of IL-2.
journal_name
Immunityjournal_title
Immunityauthors
Laurence A,Tato CM,Davidson TS,Kanno Y,Chen Z,Yao Z,Blank RB,Meylan F,Siegel R,Hennighausen L,Shevach EM,O'shea JJdoi
10.1016/j.immuni.2007.02.009subject
Has Abstractpub_date
2007-03-01 00:00:00pages
371-81issue
3eissn
1074-7613issn
1097-4180pii
S1074-7613(07)00176-8journal_volume
26pub_type
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