A role for IL-27 in limiting T regulatory cell populations

IL-27 is a cytokine that regulates Th function during autoimmune and pathogen-induced immune responses. Although previous studies have shown that regulatory T cells (Tregs) express the IL-27R, and that IL-27 inhibits forkhead box P3 upregulation in vitro, little is known about how IL-27 influences T...

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Veröffentlicht in:The Journal of immunology (1950) 2011-07, Vol.187 (1), p.266-273
Hauptverfasser: Wojno, Elia D Tait, Hosken, Nancy, Stumhofer, Jason S, O'Hara, Aisling C, Mauldin, Elizabeth, Fang, Qun, Turka, Laurence A, Levin, Steven D, Hunter, Christopher A
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Sprache:eng
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Zusammenfassung:IL-27 is a cytokine that regulates Th function during autoimmune and pathogen-induced immune responses. Although previous studies have shown that regulatory T cells (Tregs) express the IL-27R, and that IL-27 inhibits forkhead box P3 upregulation in vitro, little is known about how IL-27 influences Tregs in vivo. The studies presented in this article show that mice that overexpress IL-27 had decreased Treg frequencies and developed spontaneous inflammation. Although IL-27 did not cause mature Tregs to downregulate forkhead box P3, transgenic overexpression in vivo limited the size of a differentiating Treg population in a bone marrow chimera model, which correlated with reduced production of IL-2, a vital cytokine for Treg maintenance. These data identify an indirect role for IL-27 in shaping the Treg pool.
ISSN:0022-1767
1550-6606
DOI:10.4049/jimmunol.1004182