炎症体
托法替尼
溃疡性结肠炎
干扰素
程序性细胞死亡
Ⅰ型干扰素
免疫学
结肠炎
类有机物
信号转导
JAK-STAT信号通路
贾纳斯激酶
癌症研究
生物
医学
炎症
细胞因子
细胞凋亡
细胞生物学
内科学
酪氨酸激酶
遗传学
类风湿性关节炎
疾病
作者
Peter F. Flood,Á Fanning,Jerzy A. Woznicki,Tadhg Crowley,Andrea S. Christopher,Alessandra Vaccaro,Aileen Houston,Sheila M. McSweeney,Sarah A. Ross,Aileen Hogan,Elizabeth Brint,Agnieszka Skowyra,Milán Bustamante,Monica Ambrose,Gerard M. Moloney,John MacSharry,Marie‐Louise Hammarström,Margot Hurley,Christine Fitzgibbons,Eamonn M.M. Quigley
出处
期刊:American Journal of Physiology-gastrointestinal and Liver Physiology
[American Physiological Society]
日期:2022-09-27
卷期号:323 (5): G439-G460
被引量:34
标识
DOI:10.1152/ajpgi.00104.2022
摘要
This study found that patients with active UC have significantly increased colonic gene expression of cytosolic DNA sensor, inflammasome, STING, and type I IFN signaling pathways. The type I IFN, IFN-β, in combination with TNF-α induced JAK-dependent but NLRP3 and inflammasome-independent inflammatory cell death of colonic organoids. This novel inflammatory cell death phenotype is relevant to UC immunopathology and may partially explain the efficacy of the JAKinibs tofacitinib and upadacitinib in patients with UC.
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