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Interleukins 27 and 6 induce STAT3-mediated T cell production of interleukin 10
被引:653
作者:

Stumhofer, Jason S.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA

Silver, Jonathan S.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA

Laurence, Arian
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA

Porrett, Paige M.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA

Harris, Tajie H.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA

Turka, Laurence A.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA

Ernst, Matthias
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA

Saris, Christiaan J. M.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA

O'Shea, John J.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA

Hunter, Christopher A.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA Univ Penn, Sch Vet Med, Dept Pathobiol, Philadelphia, PA 19104 USA
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.
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页码:1363 / U5
页数:10
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