钙蛋白酶
S100A9型
炎症
S100A8型
炎症性肠病
发病机制
免疫学
疾病
模式识别受体
溃疡性结肠炎
医学
肠粘膜
生物
病理
内科学
免疫系统
免疫
作者
Dirk Foell,Helmut Wittkowski,Johannes Roth
出处
期刊:Gut
[BMJ]
日期:2009-01-09
卷期号:58 (6): 859-868
被引量:209
标识
DOI:10.1136/gut.2008.170019
摘要
It is a common experience that gastrointestinal symptoms urge us to differentiate inflammatory bowel disease (IBD) from functional disorders. Furthermore, in patients with proven IBD the disease activity has to be accurately monitored. Faecal markers of neutrophil influx into the mucosa are promising indicators of intestinal inflammation. Some neutrophil-derived proteins may be linked to the pathogenesis of IBD due to their functions as damage-associated molecular pattern molecules (DAMPs). Phagocyte-specific DAMPs of the S100 family are released from neutrophils or monocytes, followed by pro-inflammatory activation of pattern recognition receptors. The complex of S100A8/S100A9 was termed “calprotectin” and has been in use as a faecal marker for 10 years. More recently, faecal S100A12 has been reported to be an even more accurate faecal marker of inflammation. We review the biology of this novel group of molecules which can be used as surrogate markers directly linked to the molecular mechanisms of gut inflammation.
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