Sepsis-induced immunosuppression: from cellular dysfunctions to immunotherapy

被引:2263
作者
Hotchkiss, Richard S. [1 ]
Monneret, Guillaume [2 ]
Payen, Didier [3 ,4 ]
机构
[1] Washington Univ, Sch Med, Dept Anesthesiol Med & Surg, St Louis, MO 63110 USA
[2] Hop Edouard Herriot, Hosp Civils Lyon, Immunol Lab, F-69003 Lyon, France
[3] Hop Lariboisiere, AP HP, Dept Anesthesiol & Crit & Serv Mobile Urgence Rap, F-75010 Paris, France
[4] Univ Paris 07, F-75010 Paris, France
基金
美国国家卫生研究院;
关键词
REGULATORY T-CELLS; ANTIINFLAMMATORY CYTOKINE PROFILE; RECOMBINANT HUMAN INTERLEUKIN-7; INTERFERON-GAMMA PRODUCTION; INTENSIVE-CARE PATIENTS; ANTIGEN-DR EXPRESSION; BLOOD DENDRITIC CELLS; SEPTIC SHOCK PATIENTS; IMPROVES SURVIVAL; IMMUNE DYSFUNCTION;
D O I
10.1038/nri3552
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Sepsis-which is a severe life-threatening infection with organ dysfunction-initiates a complex interplay of host pro-inflammatory and anti-inflammatory processes. Sepsis can be considered a race to the death between the pathogens and the host immune system, and it is the proper balance between the often competing pro-and anti-inflammatory pathways that determines the fate of the individual. Although the field of sepsis research has witnessed the failure of many highly touted clinical trials, a better understanding of the pathophysiological basis of the disorder and the mechanisms responsible for the associated pro-and anti-inflammatory responses provides a novel approach for treating this highly lethal condition. Biomarker-guided immunotherapy that is administered to patients at the proper immune phase of sepsis is potentially a major advance in the treatment of sepsis and in the field of infectious disease.
引用
收藏
页码:862 / 874
页数:13
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