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[手术创伤相关多器官功能障碍综合征发病机制中的细胞因子风暴]

[Cytokine storm in the pathogenesis of multiple organ dysfunction syndrome associated with surgical insults].

作者信息

Aikawa N

机构信息

Department of Emergency and Critical Care Medicine, School of Medicine, Keio University, Tokyo, Japan.

出版信息

Nihon Geka Gakkai Zasshi. 1996 Sep;97(9):771-7.

PMID:8940690
Abstract

Multiple organ dysfunction syndrome (MODS) is a critical condition developing in the patients under overwhelming surgical insults such as a major surgery, severe trauma, extensive burn, and systemic sepsis. The host response to those surgical insults is the main pathogenetic factor contributing to the development of shock and MODS seen in surgical patients. The proinflammatory cytokines, TNF-alpha (TNF) and interleukin-1 beta (IL-1), are known to play a pivotal role in the pathogenetic mechanisms of MODS. In response to surgical insults, macrophages produce and release TNF and IL-1 which subsequently induce the production of other cytokines (IL-6, IL-8, etc.) and other endogenous chemical mediators (growth factors, adhesion molecules, complement cleavage products, thrombin, eicosanoids, PAF, nitric oxides, oxygen-free radicals, granulocyte elastase, etc.) The resultant systemic inflammation may develop into shock and MODS when the primary insults are overwhelming (early MODS) or a second inflammatory insult such as sepsis triggers an exaggerated inflammation. In the patients suffering from MODS, a systemic release of various cytokines is not properly regulated, and the high blood levels of the proinflammatory cytokines induce an autodestructive generalized inflammatory reaction. This condition is termed "Cytokine Storm" by the author. In the cytokine storm, not only proinflammatory cytokines but also anti-inflammatory cytokines are elevated in the blood stream. With the recent understanding of the biological and pathological roles of cytokines and other mediators, a new therapeutic strategy has been developed. In addition to the reduction of the surgical insults, a variety of anti-cytokine therapy and anti-mediator therapy has been tested in an attempt to prevent or treat the life-threatening MODS.

摘要

多器官功能障碍综合征(MODS)是在经历诸如大手术、严重创伤、大面积烧伤和全身性脓毒症等严重外科创伤的患者中发生的一种危急病症。宿主对这些外科创伤的反应是导致外科患者发生休克和MODS的主要致病因素。已知促炎细胞因子肿瘤坏死因子-α(TNF)和白细胞介素-1β(IL-1)在MODS的发病机制中起关键作用。针对外科创伤,巨噬细胞产生并释放TNF和IL-1,随后诱导其他细胞因子(IL-6、IL-8等)以及其他内源性化学介质(生长因子、黏附分子、补体裂解产物、凝血酶、类花生酸、血小板活化因子、一氧化氮、氧自由基、粒细胞弹性蛋白酶等)的产生。当原发性创伤严重(早期MODS)或诸如脓毒症等二次炎症性创伤引发过度炎症时,由此产生的全身性炎症可能发展为休克和MODS。在患有MODS的患者中,各种细胞因子的全身性释放未得到适当调节,促炎细胞因子的高血水平会引发自毁性全身性炎症反应。作者将这种情况称为“细胞因子风暴”。在细胞因子风暴中,不仅促炎细胞因子,抗炎细胞因子在血流中也会升高。随着对细胞因子和其他介质的生物学及病理作用的最新认识,已开发出一种新的治疗策略。除了减少外科创伤外,还对多种抗细胞因子疗法和抗介质疗法进行了测试,试图预防或治疗危及生命的MODS。

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