Liu Mengyuan, Wang Ting, Zhou Yun, Zhao Yutong, Zhang Yan, Li Jianping
Department of Cardiology, Peking University First Hospital, Beijing, China.
NHC Key Laboratory of Cardiovascular Molecular Biology and Regulatory Peptides, Beijing, China.
J Transl Int Med. 2020 May 9;8(1):9-19. doi: 10.2478/jtim-2020-0003. eCollection 2020 Mar.
COVID-19 is the current public health threat all over the world. Unfortunately, there is no specific prevention and treatment strategy for this disease. We aim to explore the potential role of angiotensin-converting enzyme 2 (ACE2) in this regard through this literature review. As a crucial enzyme of renin-angiotensin-aldosterone system (RAAS), ACE2 not only mediates the virus entry but also affects the pathophysiological process of virus-induced acute lung injury (ALI), as well as other organs' damage. As interaction of COVID-19 virus spike and ACE2 is essential for virus infection, COVID-19-specific vaccine based on spike protein, small molecule compound interrupting their interaction, human monoclonal antibody based on receptor-binding domain, and recombinant human ACE2 protein (rhuACE2) have aroused the interests of researchers. Meanwhile, ACE2 could catalyze angiotensin II (Ang II) to form angiotensin 1-7 (Ang 1-7), thus alleviates the harmful effect of Ang II and amplifies the protection effect of Ang1-7. ACE inhibitor and angiotensin II receptor blocker (ARB) have been shown to increase the level of expression of ACE2 and could be potential strategies in protecting lungs, heart, and kidneys. ACE2 plays a very important role in the pathogenesis and pathophysiology of COVID-19 infection. Strategies targeting ACE2 and its ligand, COVID-19 virus spike protein, may provide novel method in the prevention and management of novel coronavirus pneumonia.
2019冠状病毒病是当前全球公共卫生威胁。不幸的是,针对这种疾病尚无具体的预防和治疗策略。我们旨在通过这篇文献综述探讨血管紧张素转换酶2(ACE2)在这方面的潜在作用。作为肾素-血管紧张素-醛固酮系统(RAAS)的关键酶,ACE2不仅介导病毒进入,还影响病毒诱导的急性肺损伤(ALI)的病理生理过程以及其他器官的损伤。由于2019冠状病毒病病毒刺突蛋白与ACE2的相互作用对病毒感染至关重要,基于刺突蛋白的2019冠状病毒病特异性疫苗、阻断它们相互作用的小分子化合物、基于受体结合域的人单克隆抗体以及重组人ACE2蛋白(rhuACE2)引起了研究人员的兴趣。同时,ACE2可催化血管紧张素II(Ang II)形成血管紧张素1-7(Ang 1-7),从而减轻Ang II的有害作用并增强Ang1-7的保护作用。已证明血管紧张素转换酶抑制剂和血管紧张素II受体阻滞剂(ARB)可增加ACE2的表达水平,可能是保护肺、心脏和肾脏的潜在策略。ACE2在2019冠状病毒病感染的发病机制和病理生理学中起着非常重要的作用。针对ACE2及其配体(2019冠状病毒病病毒刺突蛋白)的策略可能为新型冠状病毒肺炎的预防和管理提供新方法。