In vitro inhibition of severe acute respiratory syndrome coronavirus by chloroquine

By E. Keyaerts, L. Vijgen, Piet Maes, J. Neyts, M. Ranst. Biochemical and Biophysical Research Communications - BBRC, 2004

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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 μM) was significantly lower than its cytostatic activity; CC50 (261.3 ± 14.5 μM), 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.

Subfields: Computational Theory and Mathematics, Infectious Diseases

View Paper: https://www.semanticscholar.org/paper/1854d80a095c32aaa524e50d07756a51493d5917

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