4.7 Review

New approaches to the study of sepsis

Journal

EMBO MOLECULAR MEDICINE
Volume 4, Issue 12, Pages 1234-1243

Publisher

WILEY
DOI: 10.1002/emmm.201201375

Keywords

clinical trials; complement; interventions; mediators; sepsis

Funding

  1. National Institutes of Health [GM-29507, GM-61656]

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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.

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