Nonresolving Inflammation

被引:1723
作者
Nathan, Carl [1 ,2 ]
Ding, Aihao [1 ,2 ]
机构
[1] Cornell Univ, Weill Cornell Med Coll, Dept Microbiol & Immunol, New York, NY 10065 USA
[2] Cornell Univ, Weill Grad Sch Med Sci, Program Immunol & Microbial Pathogenesis, New York, NY 10065 USA
关键词
CHRONIC GRANULOMATOUS-DISEASE; ACUTE LUNG INJURY; APOPTOTIC CELLS; IMMUNE-SYSTEM; NITRIC-OXIDE; ANTIINFLAMMATORY PROPERTIES; MEDIATED INFLAMMATION; AIRWAY INFLAMMATION; DEPENDENT CLEARANCE; PULMONARY-FIBROSIS;
D O I
10.1016/j.cell.2010.02.029
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nonresolving inflammation is a major driver of disease. Perpetuation of inflammation is an inherent risk because inflammation can damage tissue and necrosis can provoke inflammation. Nonetheless, multiple mechanisms normally ensure resolution. Cells like macrophages switch phenotypes, secreted molecules like reactive oxygen intermediates switch impact from pro- to anti-inflammatory, and additional mediators of resolution arise, including proteins, lipids, and gasses. Aside from persistence of initiating stimuli, nonresolution may result from deficiencies in these mechanisms when an inflammatory response begins either excessively or subnormally. This greatly complicates the development of anti-inflammatory therapies. The problem calls for conceptual, organizational, and statistical innovations.
引用
收藏
页码:871 / 882
页数:12
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