- Author:
Yong-Zheng GUO
1
;
Kai-Jin XU
1
;
Yong-Tao LI
1
;
Jia-Dan FU
1
;
Min XU
1
;
Ling YU
1
;
Ji-Fang SHENG
1
;
Biao ZHU
1
Author Information
- Publication Type:Journal Article
- Keywords: SARS-CoV; Lopinavir; Darunavir; Pneumonia; Lipid metabolism
- MeSH: Adult; COVID-19/drug therapy*; China; Darunavir; Drug Combinations; Female; Humans; Indoles/therapeutic use*; Lipid Metabolism; Lopinavir; Male; Middle Aged; Protease Inhibitors/therapeutic use*; Retrospective Studies; Ritonavir; SARS-CoV-2/genetics*
- From: Journal of Zhejiang University. Science. B 2020;21(12):948-954
- CountryChina
- Language:English
- Abstract: The aim of this study was to evaluate the safety of an antiviral regimen of protease inhibitors combined with Arbidol (umifenovir) for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pneumonia patients. The genomic sequence of SARS-CoV-2 is highly homologous to that of SARS-CoV (Zhou et al., 2020). Previously published basic and clinical research on anti-SARS-CoV treatment found that lopinavir/ritonavir (LPV/r) could improve the prognosis of SARS patients (Chan et al., 2003; Chu et al., 2004). Darunavir (DRV) is another protease inhibitor that blocks the binding of SARS-CoV-2 to human angiotensin-converting enzyme 2 (Omotuyi et al., 2020). The broad-spectrum antiviral drug Arbidol (umifenovir) also shows in vitro anti-SARS-CoV activity (Khamitov et al., 2008).