Jiang Honghong, Guo Yiming, Wang Qihang, Wang Yiran, Peng Dingchuan, Fang Yigong, Yan Lei, Ruan Zhuolin, Zhang Sheng, Zhao Yong, Zhang Wendan, Shang Wei, Feng Zhichun
Faculty of Pediatrics, the Seventh Medical Center of Chinese PLA General Hospital National Engineering Laboratory for Birth Defects Prevention and Control of Key Technology, Beijing Key Laboratory of Pediatric Organ Failure Beijing China.
Department of Biological Science, The Dietrich School of Arts and Sciences University of Pittsburgh Pittsburgh Pennsylvania USA.
MedComm (2020). 2024 Oct 23;5(11):e785. doi: 10.1002/mco2.785. eCollection 2024 Nov.
The complement system, comprising over 30 proteins, is integral to the immune system, and the coagulation system is critical for vascular homeostasis. The activation of the complement and coagulation systems involves an organized proteolytic cascade, and the overactivation of these systems is a central pathogenic mechanism in several diseases. This review describes the role of complement and coagulation system activation in critical illness, particularly sepsis. The complexities of sepsis reveal significant knowledge gaps that can be compared to a profound abyss, highlighting the urgent need for further investigation and exploration. It is well recognized that the inflammatory network, coagulation, and complement systems are integral mechanisms through which multiple factors contribute to increased susceptibility to infection and may result in a disordered immune response during septic events in patients. Given the overlapping pathogenic mechanisms in sepsis, immunomodulatory therapies currently under development may be particularly beneficial for patients with sepsis who have concurrent infections. Herein, we present recent findings regarding the molecular relationships between the coagulation and complement pathways in the advancement of sepsis, and propose potential intervention targets related to the crosstalk between coagulation and complement, aiming to provide more valuable treatment of sepsis.
补体系统由30多种蛋白质组成,是免疫系统不可或缺的一部分,而凝血系统对血管稳态至关重要。补体系统和凝血系统的激活涉及一个有组织的蛋白水解级联反应,这些系统的过度激活是多种疾病的核心致病机制。本综述描述了补体和凝血系统激活在危重病,尤其是脓毒症中的作用。脓毒症的复杂性揭示了巨大的知识空白,堪比深邃的深渊,凸显了进一步研究和探索的迫切需求。众所周知,炎症网络、凝血和补体系统是多种因素导致感染易感性增加并可能在患者脓毒症事件期间导致免疫反应紊乱的不可或缺的机制。鉴于脓毒症中存在重叠的致病机制,目前正在研发的免疫调节疗法可能对同时发生感染的脓毒症患者特别有益。在此,我们介绍了脓毒症进展过程中凝血和补体途径之间分子关系的最新研究结果,并提出了与凝血和补体之间相互作用相关的潜在干预靶点,旨在为脓毒症提供更有价值的治疗方法。