Interleukins 27 and 6 induce STAT3-mediated T cell production of interleukin 10

被引:653
作者
Stumhofer, Jason S.
Silver, Jonathan S.
Laurence, Arian
Porrett, Paige M.
Harris, Tajie H.
Turka, Laurence A.
Ernst, Matthias
Saris, Christiaan J. M.
O'Shea, John J.
Hunter, Christopher A. [1 ]
机构
[1] Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA
[2] NIAMSD, Mol Immunol & Inflammat Branch, NIH, Bethesda, MD 20892 USA
[3] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[4] Ludwig Inst Canc Res, Parkville, Vic 3050, Australia
[5] Amgen Inc, Dept Inflammat Res, Thousand Oaks, CA 91320 USA
关键词
D O I
10.1038/ni1537
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interleukin 10 (IL-10) has a prominent function in regulating the balance between protective and pathological T cell responses. Consistent with that activity, many sources of this cytokine are found in vivo, including from myeloid cells and a variety of T cell subsets. However, although there are many pathways that regulate innate production of IL-10, the factors that govern its synthesis by the adaptive response are poorly understood. Here we report that IL-27 and IL-6 induced T helper type 1 and type 2 cells, as well as T helper cells that produce IL-17, to secrete IL-10. This effect was dependent on the transcription factors STAT1 and STAT3 for IL-27 and on STAT3 for IL-6. Our studies identify a previously unknown pathway that allows the immune system to temper inflammatory responses.
引用
收藏
页码:1363 / U5
页数:10
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