Cytokine Networks in the Pathophysiology of Inflammatory Bowel Disease

被引:595
作者
Friedrich, Matthias [1 ]
Pohin, Mathilde [1 ]
Powrie, Fiona [1 ,2 ]
机构
[1] Univ Oxford, Kennedy Inst Rheumatol, Nuffield Dept Orthopaed Rheumatol & Musculoskelet, Roosevelt Dr, Oxford OX3 7FY, England
[2] Univ Oxford, John Radcliffe Hosp, Expt Med Div, Nuffield Dept Med,Translat Gastroenterol Unit, Oxford OX3 9DU, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
INNATE LYMPHOID-CELLS; CHRONIC INTESTINAL INFLAMMATION; SEVERE CROHNS-DISEASE; ANTIINTERFERON-GAMMA ANTIBODY; GENOME-WIDE ASSOCIATION; GROWTH-FACTOR-BETA; CD4(+) T-CELLS; DOUBLE-BLIND; MONOCLONAL-ANTIBODY; ULCERATIVE-COLITIS;
D O I
10.1016/j.immuni.2019.03.017
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Inflammatory bowel disease (IBD) is a chronic inflammatory disease of the gastrointestinal tract. Cytokine-targeted therapies have transformed the treatment of IBD, providing control of symptoms and longer relapse-free periods. However, many patients fail to respond, highlighting the need for therapies tailored to the underlying cell and molecular disease drivers. Here we discuss the progression of IBD from the perspective of remodeling of cytokine networks. We place well-established and under-studied cytokine modules in the context of cellular interactions, their dynamic regulation in early and late stages of disease (i.e., fibrosis), and their current and potential use in the clinic. Examining how particular cytokine networks drive distinct features and phases of IBD will shed light on the etiology of IBD and provide a basis for more effective treatments.
引用
收藏
页码:992 / 1006
页数:15
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