Golestan Hospital Clinical Research Development Unit, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Department of Microbiology, Sciences, and Research Branch, Islamic Azad University, Fars, Iran.
Iran J Immunol. 2023 Sep 1;20(3):247-261. doi: 10.22034/iji.2023.97585.2522.
Two central questions in COVID-19 treatment which should be considered are: "How does the imbalance of the complement system affect the therapeutic approaches?" and "Do we consider complement inhibitors in therapeutic protocols?". The complement system is a double-edged sword since it may either promote immune responses against COVID-19 or contribute to destructive inflammation in the host. Therefore, it is crucial to regulate this system with complement inhibitors. In this manuscript, we discuss the molecular mechanisms of complement and complement inhibitors in COVID-19 patients. We searched the terms "COVID-19", "Complement", "Complement inhibitor", "SARS-CoV-2", and all complement fragments and inhibitors from 2000 to 2022 in PubMed and google scholar and checked the pathways in "KEGG pathway database". Complement is not well-appreciated in the treatment protocols despite its multiple roles in the disease, and most of the preventive anti-inflammatory therapeutic approaches did not include a complement inhibitor in COVID-19 therapeutic protocols. In this review article, we discussed the most recent studies regarding complement components mediated interventions and the mechanism of these interventions in COVID-19 patients. Since the control of the complement system overactivation is associated with a better prognosis in the initial stages of COVID-19, heparin, anti-thrombin, C1-inhibitor, montelukast, and hydralazine can be effective in the initial stages of this viral infection. Recombinant complement activation (RCA) proteins are more effective in regulating complement compared to terminal pathway therapeutic approaches such as the C3a and C5a inhibitors.
在 COVID-19 治疗中,有两个核心问题需要考虑:“补体系统失衡如何影响治疗方法?”和“我们是否考虑在治疗方案中使用补体抑制剂?”。补体系统是一把双刃剑,因为它既可以促进针对 COVID-19 的免疫反应,也可以导致宿主的破坏性炎症。因此,用补体抑制剂来调节这个系统是至关重要的。在本文中,我们讨论了补体系统和补体抑制剂在 COVID-19 患者中的分子机制。我们在 PubMed 和谷歌学术上以“COVID-19”、“补体”、“补体抑制剂”、“SARS-CoV-2”和所有补体片段和抑制剂为关键词进行了 2000 年至 2022 年的搜索,并检查了“KEGG 途径数据库”中的途径。尽管补体在疾病中有多种作用,但它在治疗方案中并没有得到很好的应用,而且大多数预防性抗炎治疗方法都没有在 COVID-19 治疗方案中包括补体抑制剂。在这篇综述文章中,我们讨论了关于补体成分介导的干预措施的最新研究以及这些干预措施在 COVID-19 患者中的作用机制。由于控制补体系统的过度激活与 COVID-19 患者的早期预后相关,肝素、抗凝血酶、C1 抑制剂、孟鲁司特和肼屈嗪在这种病毒感染的早期可能是有效的。与末端途径治疗方法(如 C3a 和 C5a 抑制剂)相比,重组补体激活(RCA)蛋白在调节补体方面更有效。