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确定预防和治疗的可用策略:从ACE2的角度探索2019冠状病毒病(综述)

Determining available strategies for prevention and therapy: Exploring COVID‑19 from the perspective of ACE2 (Review).

作者信息

Cai Liyang, Guo Xi, Cao Yuchen, Ying Peixi, Hong Libing, Zhang Yuxi, Yi Guoguo, Fu Min

机构信息

The Second Clinical School, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China.

Medical College of Rehabilitation, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China.

出版信息

Int J Mol Med. 2021 Apr;47(4). doi: 10.3892/ijmm.2021.4876. Epub 2021 Feb 12.

DOI:10.3892/ijmm.2021.4876
PMID:33576441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7891831/
Abstract

Coronavirus disease 2019 (COVID‑19) is an acute infectious pneumonia caused by a novel type of coronavirus infection. There are currently no clinically available specific drugs for the treatment of this virus. The process of host invasion is the key to viral infection, and it is a mechanism that needs to be considered when exploring antiviral drugs. At present, studies have confirmed that angiotensin‑converting enzyme II (ACE2) is the main functional receptor through which severe acute respiratory syndrome coronavirus (SARS‑CoV‑2) invades host cells. Therefore, a number of studies have focused on this field. However, as ACE2 may play a dual role in mediating susceptibility and immunity to SARS‑CoV‑2 infection, the role of ACE2 in viral infection is controversial. Beginning with the physiological function of ACE2, the present review article summarizes the influence of the ACE2 content on the susceptibility to the virus and acute lung injury. Drug mechanisms were taken as the starting point, combined with the results of clinical trials, specifically elaborating upon and analyzing the efficacy of several ACE2‑centered therapeutic drugs and their potential effects. In addition, the current status of ACE2 as a targeted therapy for COVID‑19 is discussed in order to provide new insight into the clinical prevention and treatment of COVID‑19.

摘要

2019冠状病毒病(COVID-19)是由一种新型冠状病毒感染引起的急性感染性肺炎。目前临床上尚无治疗该病毒的特效药物。宿主入侵过程是病毒感染的关键,也是探索抗病毒药物时需要考虑的一种机制。目前,研究已证实血管紧张素转换酶II(ACE2)是严重急性呼吸综合征冠状病毒(SARS-CoV-2)入侵宿主细胞的主要功能性受体。因此,许多研究都聚焦于这一领域。然而,由于ACE2在介导对SARS-CoV-2感染的易感性和免疫方面可能发挥双重作用,其在病毒感染中的作用存在争议。本文从ACE2的生理功能入手,总结了ACE2含量对病毒易感性和急性肺损伤的影响。以药物机制为出发点,结合临床试验结果,具体阐述并分析了几种以ACE2为中心的治疗药物的疗效及其潜在作用。此外,还讨论了ACE2作为COVID-19靶向治疗的现状,以期为COVID-19的临床防治提供新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4725/7891831/f07e42aa590c/IJMM-47-04-04876-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4725/7891831/5adc2ba7eb30/IJMM-47-04-04876-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4725/7891831/9c77fb741ddd/IJMM-47-04-04876-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4725/7891831/05e8ad439b8a/IJMM-47-04-04876-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4725/7891831/f07e42aa590c/IJMM-47-04-04876-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4725/7891831/5adc2ba7eb30/IJMM-47-04-04876-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4725/7891831/9c77fb741ddd/IJMM-47-04-04876-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4725/7891831/05e8ad439b8a/IJMM-47-04-04876-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4725/7891831/f07e42aa590c/IJMM-47-04-04876-g03.jpg

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