Potential therapeutic effects of dipyridamole in the severely ill patients with COVID-19

被引:151
|
作者
Liu, Xiaoyan [1 ]
Li, Zhe [2 ]
Liu, Shuai [1 ,3 ]
Sun, Jing [4 ]
Chen, Zhanghua [5 ,6 ]
Jiang, Min [7 ,8 ]
Zhang, Qingling [4 ]
Wei, Yinghua [7 ,8 ]
Wang, Xin [9 ]
Huang, Yi-You [2 ]
Shi, Yinyi [3 ]
Xu, Yanhui [5 ]
Xian, Huifang [5 ]
Bai, Fan [6 ]
Ou, Changxing [4 ]
Xiong, Bei [1 ]
Lew, Andrew M. [10 ,11 ]
Cui, Jun [12 ]
Fang, Rongli [5 ]
Huang, Hui [13 ]
Zhao, Jincun [4 ]
Hong, Xuechuan [14 ,15 ]
Zhang, Yuxia [5 ]
Zhou, Fuling [1 ]
Luo, Hai-Bin [2 ]
机构
[1] Wuhan Univ, Dept Hematol, Zhongnan Hosp, Wuhan 430071, Peoples R China
[2] Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangdong Prov Key Lab New Drug Design & Evaluat, Guangzhou 510006, Peoples R China
[3] Dawu Cty Peoples Hosp, Xiaogan 432826, Peoples R China
[4] Guangzhou Med Univ, Affiliated Hosp 1, Guangzhou Inst Resp Hlth, State Key Lab Resp Dis,Natl Clin Res Ctr Resp Dis, Guangzhou 510120, Peoples R China
[5] Guangzhou Med Univ, State Key Lab Resp Dis, Guangzhou Women & Childrens Med Ctr, Guangzhou Inst Pediat, Guangzhou 510623, Peoples R China
[6] Peking Univ, Sch Life Sci, Biomed Pioneering Innovat Ctr BIOPIC, Beijing 100871, Peoples R China
[7] Guangxi Med Univ, Affiliated Hosp 1, Dept Infect Dis, Nanning 530021, Peoples R China
[8] Guangxi Med Univ, Affiliated Hosp 1, Dept Pediat, Nanning 530021, Peoples R China
[9] Ocean Univ China, Sch Med & Pharm, Ctr Innovat Marine Drug Screening & Evaluat QNLM, Qingdao 266100, Peoples R China
[10] Univ Melbourne, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3052, Australia
[11] Univ Melbourne, Dept Microbiol & Immunol, Parkville, Vic 3052, Australia
[12] Sun Yat Sen Univ, Sch Life Sci, Guangzhou 510006, Peoples R China
[13] Sun Yat Sen Univ, Affiliated Hosp 8, Cardiovasc Dept, Shenzhen 518000, Peoples R China
[14] Tibet Univ, Coll Med, State Key Lab Virol,Coll Sci, Innovat Ctr Tradit Tibetan Med Modernizat & Qual, Lhasa 850000, Peoples R China
[15] Wuhan Univ, Sch Pharmaceut Sci, Key Lab Combinatorial Biosynth & Drug Discovery, MOE,Hubei Prov Engn & Technol Res Ctr Fluorinated, Wuhan 430071, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Dipyridamole; SARS-CoV-2; COVID-19; Treatment; D-dimer; Severe cases; ANGIOTENSIN-CONVERTING ENZYME-2; CLINICAL CHARACTERISTICS; CORONAVIRUS; ACE2; INHIBITION; PNEUMONIA;
D O I
10.1016/j.apsb.2020.04.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection can cause acute respiratory distress syndrome, hypercoagulability, hypertension, and multiorgan dysfunction. Effective antivirals with safe clinical profile are urgently needed to improve the overall prognosis. In an analysis of a randomly collected cohort of 124 patients with COVID-19, we found that hypercoagulability as indicated by elevated concentrations of D-dimers was associated with disease severity. By virtual screening of a U.S. FDA approved drug library, we identified an anticoagulation agent dipyridamole (DIP) in silico, which suppressed SARS-CoV-2 replication in vitro. In a proof-of-concept trial involving 31 patients with COVID-19, DIP supplementation was associated with significantly decreased concentrations of D-dimers (P < 0.05), increased lymphocyte and platelet recovery in the circulation, and markedly improved clinical outcomes in comparison to the control patients. In particular, all 8 of the DIP-treated severely ill patients showed remarkable improvement: 7 patients (87.5%) achieved clinical cure and were discharged from the hospitals while the remaining 1 patient (12.5%) was in clinical remission. (C) 2020 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.
引用
收藏
页码:1205 / 1215
页数:11
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