Ward Peter A
Department of Pathology, University of Michigan Medical School, 1301 Catherine Road, Ann Arbor, Michigan 48109, USA.
Nat Rev Immunol. 2004 Feb;4(2):133-42. doi: 10.1038/nri1269.
Sepsis is a major clinical problem for which therapeutic interventions have been largely unsuccessful, in spite of promising strategies that were successful in animals, especially rodents. There is new evidence that sepsis causes excessive activation of the complement system and that this induces paralysis of innate immune functions in phagocytic cells due to effects of the powerful complement-activation product, C5a. This review describes our present understanding of how and why sepsis is a life-threatening condition and how it might be more effectively treated.
脓毒症是一个主要的临床问题,尽管在动物尤其是啮齿动物身上取得成功的有前景的策略,但针对它的治疗干预在很大程度上并不成功。有新证据表明,脓毒症会导致补体系统过度激活,并且由于强大的补体激活产物C5a的作用,这会诱导吞噬细胞的固有免疫功能麻痹。这篇综述描述了我们目前对脓毒症如何以及为何是一种危及生命的病症的理解,以及它如何能够得到更有效的治疗。