New approaches to the study of sepsis

被引:116
作者
Ward, Peter A. [1 ]
机构
[1] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
clinical trials; complement; interventions; mediators; sepsis; ANIMAL-MODELS; CECAL LIGATION; CYTOKINE REMOVAL; SEPTIC SHOCK; C5A; GENDER; THERAPY; ANTIBODIES; ENDOTOXIN; GUT;
D O I
10.1002/emmm.201201375
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Models of sepsis have been instructive in understanding the sequence of events in animals and, to an extent, in humans with sepsis. Events developing early in sepsis suggest that a hyperinflammatory state exists, accompanied by a buildup of oxidants in tissues reflective of a redox imbalance. Development of immunosuppression and degraded innate and adaptive immune responses are well-established complications of sepsis. In addition, there is robust activation of the complement system, which contributes to the harmful effects of sepsis. These events appear to be associated with development of multiorgan failure. The relevance of animal models of sepsis to human sepsis and the failure of human clinical trials are discussed, together with suggestions as to how clinical trial design might be improved.
引用
收藏
页码:1234 / 1243
页数:10
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