In vitro inhibition of severe acute respiratory syndrome coronavirus by chloroquine

被引:516
作者
Keyaerts, E [1 ]
Vijgen, L [1 ]
Maes, P [1 ]
Neyts, J [1 ]
Van Ranst, M [1 ]
机构
[1] Katholieke Univ Leuven, Rega Inst Med Res, B-3000 Louvain, Belgium
关键词
SARS-CoV; severe acute respiratory syndrome; coronavirus; chloroquine; antiviral activity;
D O I
10.1016/j.bbrc.2004.08.085
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report on chloroquine, a 4-amino-quinoline, as an effective inhibitor of the replication of the severe acute respiratory syndrome coronavirus (SARS-CoV) in vitro. Chloroquine is a clinically approved drug effective against malaria. We tested chloroquine phosphate for its antiviral potential against SARS-CoV-induced cytopathicity in Vero E6 cell culture. Results indicate that the IC50 of chloroquine for antiviral activity (8.8 +/- 1.2 muM) was significantly lower than its cytostatic activity; CC50 (261.3 +/- 14.5 muM), yielding a selectivity index of 30. The IC50 of chloroquine for inhibition of SARS-CoV in vitro approximates the plasma concentrations of chloroquine reached during treatment of acute malaria. Addition of chloroquine to infected cultures could be delayed for up to 5 h postinfection, without an important drop in antiviral activity. Chloroquine, an old antimalarial drug, may be considered for immediate use in the prevention and treatment of SARS-CoV infections. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:264 / 268
页数:5
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