A Role for IL-27 in Limiting T Regulatory Cell Populations
Author(s) -
Elia D. Tait Wojno,
Nancy Hosken,
Jason S. Stumhofer,
Aisling O’Hara,
Elizabeth A. Mauldin,
Qun Fang,
Laurence A. Turka,
Steven D. Levin,
Christopher A. Hunter
Publication year - 2011
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1004182
Subject(s) - downregulation and upregulation , immunology , biology , immune system , cytokine , transgene , in vivo , immune tolerance , population , microbiology and biotechnology , inflammation , bone marrow , medicine , gene , genetics , environmental health
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.
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