| Literature DB >> 21622862 |
Elia D Tait Wojno1, Nancy Hosken, Jason S Stumhofer, Aisling C O'Hara, Elizabeth Mauldin, Qun Fang, Laurence A Turka, Steven D Levin, Christopher A Hunter.
Abstract
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.Entities:
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Year: 2011 PMID: 21622862 PMCID: PMC3119737 DOI: 10.4049/jimmunol.1004182
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422