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补体系统激活:连接生理学、病理生理学和治疗学。

Complement system activation: bridging physiology, pathophysiology, and therapy.

机构信息

Intensive Care Unit, Saint-Louis University Hospital, AP-HP, Paris Cité University, Paris, France.

Department of Kidney and Metabolic Diseases, Transplantation and Clinical Immunology, Necker University Hospital, AP-HP, Paris, France.

出版信息

Intensive Care Med. 2024 Nov;50(11):1791-1803. doi: 10.1007/s00134-024-07611-4. Epub 2024 Sep 10.

Abstract

The complement system is a set of over 50 proteins that constitutes an essential part of the innate immune system. Complement system activation involves an organized proteolytic cascade. Overactivation of complement system activation is the main pathogenic mechanism of several diseases and contributes to the manifestations of many other conditions. This review describes the normal complement system and the role for complement dysregulation in critical illnesses, notably sepsis and acute respiratory distress syndrome. Complement activation is involved in the immune system response to pathogens but, when excessive, can contribute to tissue damage, runaway inflammation, and capillary leakage syndrome. Complement overactivation may play a key role in severe forms of coronavirus disease 2019 (COVID-19). Two diseases whose manifestations are mainly caused by complement overactivation, namely, atypical hemolytic and uremic syndrome (aHUS) and myasthenia gravis, are discussed. A diagnostic algorithm for aHUS is provided. Early complement-inhibiting therapy has been proven effective. When renal transplantation is required, complement-inhibiting drugs can be used prophylactically to prevent aHUS recurrence. Similarly, acetylcholine-receptor autoantibody-positive generalized myasthenia gravis involves complement system overactivation and responds to complement inhibition. The two main complement inhibitors used in to date routine are eculizumab and ravulizumab. The main adverse event is Neisseria infection, which is rare and preventable, but can be fatal. The complement system is crucial to health but, when overactivated, can cause or contribute to disease. Effective complement inhibitors are now available, although additional data are required to determine optimal regimens. Further research is also needed to better understand the complement system, develop advanced diagnostic tools, and identify markers that allow the personalization of treatment strategies.

摘要

补体系统是一组超过 50 种蛋白质,构成固有免疫系统的重要组成部分。补体系统的激活涉及有序的蛋白水解级联反应。补体系统的过度激活是几种疾病的主要发病机制,并导致许多其他疾病的表现。本综述描述了正常的补体系统以及补体失调在危重病中的作用,特别是脓毒症和急性呼吸窘迫综合征。补体激活参与了免疫系统对病原体的反应,但当过度激活时,可导致组织损伤、炎症失控和毛细血管渗漏综合征。补体过度激活可能在严重的 2019 年冠状病毒病(COVID-19)中发挥关键作用。讨论了两种主要由补体过度激活引起的疾病,即非典型溶血尿毒症综合征(aHUS)和重症肌无力。提供了 aHUS 的诊断算法。已证明早期的补体抑制治疗有效。当需要肾移植时,可以使用补体抑制药物进行预防性治疗以防止 aHUS 复发。同样,乙酰胆碱受体自身抗体阳性的全身性重症肌无力也涉及补体系统的过度激活,并对补体抑制有反应。迄今为止常规使用的两种主要补体抑制剂是依库珠单抗和拉维珠单抗。主要的不良反应是奈瑟菌感染,虽然罕见且可预防,但可能致命。补体系统对健康至关重要,但过度激活时可引起或导致疾病。现在已经有有效的补体抑制剂,但需要更多的数据来确定最佳方案。还需要进一步研究以更好地了解补体系统,开发先进的诊断工具,并确定允许个性化治疗策略的标志物。

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