败血症
发病机制
免疫学
免疫系统
病理生理学
医学
炎症
下调和上调
主机响应
细胞凋亡
淋巴细胞
生物
病理
生物化学
基因
作者
Deborah J. Stearns-Kurosawa,Marcin F. Osuchowski,Catherine Valentine,Shinichiro Kurosawa,Daniel G. Remick
出处
期刊:Annual Review of Pathology-mechanisms of Disease
[Annual Reviews]
日期:2011-01-24
卷期号:6 (1): 19-48
被引量:509
标识
DOI:10.1146/annurev-pathol-011110-130327
摘要
Sepsis is a serious clinical condition that represents a patient's response to a severe infection and has a very high mortality rate. Normal immune and physiologic responses eradicate pathogens, and the pathophysiology of sepsis is due to the inappropriate regulation of these normal reactions. In an ideal scenario, the first pathogen contact with the inflammatory system should eliminate the microbe and quickly return the host to homeostasis. The septic response may accelerate due to continued activation of neutrophils and macrophages/monocytes. Upregulation of lymphocyte costimulatory molecules and rapid lymphocyte apoptosis, delayed apoptosis of neutrophils, and enhanced necrosis of cells/tissues also contribute to the pathogenesis of sepsis. The coagulation system is closely tied to the inflammatory response, with cross talk between the two systems driving the dysregulated response. Biomarkers may be used to help diagnose patients with sepsis, and they may also help to identify patients who would benefit from immunomodulatory therapies.
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