IL-4 inhibits TGF-β-induced Foxp3+ T cells and, together with TGF-β, generates IL-9+ IL-10+ Foxp3- effector T cells

被引:862
作者
Dardalhon, Valerie [1 ]
Awasthi, Amit [1 ]
Kwon, Hyoung [1 ]
Galileos, George [1 ]
Gao, Wenda [2 ]
Sobel, Raymond A. [3 ,4 ]
Mitsdoerffer, Meike [1 ]
Strom, Terry B. [2 ]
Elyaman, Wassim [1 ]
Ho, I-Cheng [5 ]
Khoury, Samia [1 ]
Oukka, Mohamed [1 ]
Kuchroo, Vijay K. [1 ]
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Ctr Neurol Dis, Cambridge, MA 02139 USA
[2] Harvard Univ, Sch Med, Beth Israel Hosp, Transplant Res Ctr, Boston, MA 02115 USA
[3] Stanford Univ, Sch Med, Dept Pathol, Palo Alto, CA 94304 USA
[4] Stanford Univ, Sch Med, Palo Alto Vet Adm Hlth Care Syst, Palo Alto, CA 94304 USA
[5] Harvard Univ, Sch Med, Dept Pediat Oncol, Div Pediat Hematol Oncol,Childrens Hosp, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/ni.1677
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Transcription factor Foxp3 is critical for generating regulatory T cells (T-reg cells). Transforming growth factor-beta (TGF-beta) induces Foxp3 and suppressive T-reg cells from naive T cells, whereas interleukin 6 (IL-6) inhibits the generation of inducible Treg cells. Here we show that IL-4 blocked the generation of TGF-beta-induced Foxp3(+) T-reg cells and instead induced a population of T helper cells that produced IL-9 and IL-10. The IL-9(+)IL-10(+) T cells demonstrated no regulatory properties despite producing abundant IL-10. Adoptive transfer of IL-9(+)IL-10(+) T cells into recombination-activating gene 1-deficient mice induced colitis and peripheral neuritis, the severity of which was aggravated if the IL-9(+)IL-10(+) T cells were transferred with CD45RB(hi) CD4(+) effector T cells. Thus IL-9(+)IL-10(+) T cells lack suppressive function and constitute a distinct population of helper-effector T cells that promote tissue inflammation.
引用
收藏
页码:1347 / 1355
页数:9
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