TH9 cells that express the transcription factor PU.1 drive T cell-mediated colitis via IL-9 receptor signaling in intestinal epithelial cells

被引:362
作者
Gerlach, Katharina [1 ]
Hwang, YouYi [2 ]
Nikolaev, Alexej [3 ]
Atreya, Raja [1 ]
Dornhoff, Heike [1 ]
Steiner, Stefanie [1 ]
Lehr, Hans-Anton [4 ]
Wirtz, Stefan [1 ]
Vieth, Michael [5 ]
Waisinan, Ari [3 ]
Rosenbauer, Frank [6 ]
McKenzie, Andrew N. J. [2 ]
Weigmann, Benno [1 ]
Neurath, Markus F. [1 ]
机构
[1] Univ Erlangen Nurnberg, Dept Med 1, D-91054 Erlangen, Germany
[2] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
[3] Univ Med Ctr Mainz, Inst Mol Med, Mainz, Germany
[4] Inst Pathol, Friedrichshafen, Germany
[5] Bayreuth Clin, Inst Pathol, Bayreuth, Germany
[6] Univ Munster, Lab Mol Stem Cell Biol, D-48149 Munster, Germany
基金
英国医学研究理事会; 英国惠康基金;
关键词
INFLAMMATORY-BOWEL-DISEASE; ULCERATIVE-COLITIS; TIGHT JUNCTIONS; TH2; CYTOKINE; TGF-BETA; DIFFERENTIATION; OVEREXPRESSION; INDUCTION; IMMUNITY; PROMOTES;
D O I
10.1038/ni.2920
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The molecular checkpoints that drive inflammatory bowel diseases are incompletely understood. Here we found more T cells expressing the transcription factor PU.1 and interleukin 9 (IL-9) in patients with ulcerative colitis. In an animal model, citrine reporter mice had more IL-9-expressing mucosal T cells in experimental oxazolone-induced colitis. IL-9 deficiency suppressed acute and chronic colitis. Mice with PU.1 deficiency in T cells were protected from colitis, whereas treatment with antibody to IL-9 suppressed colitis. Functionally, IL-9 impaired intestinal barrier function and prevented mucosal wound healing in vivo. Thus, our findings suggest that the T(H)9 subset of helper T cells serves an important role in driving ulcerative colitis by regulating intestinal epithelial cells and that T(H)9 cells represent a likely target for the treatment of chronic intestinal inflammation.
引用
收藏
页码:676 / 686
页数:11
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