结肠炎
免疫学
转录因子
溃疡性结肠炎
白细胞介素9
炎症
T辅助细胞
癌症研究
白细胞介素23
生物
白细胞介素
医学
细胞生物学
白细胞介素17
T细胞
免疫系统
细胞因子
病理
基因
疾病
生物化学
作者
Katharina Gerlach,Youyi Hwang,Alexej Nikolaev,Raja Atreya,Heike Dornhoff,Stefanie Steiner,Hans‐Anton Lehr,Stefan Wirtz,Michael Vieth,Ari Waisman,Frank Rosenbauer,Andrew N. J. McKenzie,Benno Weigmann,Markus F. Neurath
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 TH9 subset of helper T cells serves an important role in driving ulcerative colitis by regulating intestinal epithelial cells and that TH9 cells represent a likely target for the treatment of chronic intestinal inflammation.
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