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Antimalarial drugs inhibit the replication of SARS-CoV-2: An in vitro evaluation.

Identifieur interne : 000C42 ( Main/Corpus ); précédent : 000C41; suivant : 000C43

Antimalarial drugs inhibit the replication of SARS-CoV-2: An in vitro evaluation.

Auteurs : Mathieu Gendrot ; Julien Andreani ; Manon Boxberger ; Priscilla Jardot ; Isabelle Fonta ; Marion Le Bideau ; Isabelle Duflot ; Joel Mosnier ; Clara Rolland ; Hervé Bogreau ; Sébastien Hutter ; Bernard La Scola ; Bruno Pradines

Source :

RBID : pubmed:32916297

English descriptors

Abstract

In December 2019, a new severe acute respiratory syndrome coronavirus (SARS-CoV-2) causing coronavirus diseases 2019 (COVID-19) emerged in Wuhan, China. African countries see slower dynamic of COVID-19 cases and deaths. One of the assumptions that may explain this later emergence in Africa, and more particularly in malaria endemic areas, would be the use of antimalarial drugs. We investigated the in vitro antiviral activity against SARS-CoV-2 of several antimalarial drugs. Chloroquine (EC50 = 2.1 μM and EC90 = 3.8 μM), hydroxychloroquine (EC50 = 1.5 μM and EC90 = 3.0 μM), ferroquine (EC50 = 1.5 μM and EC90 = 2.4 μM), desethylamodiaquine (EC50 = 0.52 μM and EC90 = 1.9 μM), mefloquine (EC50 = 1.8 μM and EC90 = 8.1 μM), pyronaridine (EC50 = 0.72 μM and EC90 = 0.75 μM) and quinine (EC50 = 10.7 μM and EC90 = 38.8 μM) showed in vitro antiviral effective activity with IC50 and IC90 compatible with drug oral uptake at doses commonly administered in malaria treatment. The ratio Clung/EC90 ranged from 5 to 59. Lumefantrine, piperaquine and dihydroartemisinin had IC50 and IC90 too high to be compatible with expected plasma concentrations (ratio Cmax/EC90 < 0.05). Based on our results, we would expect that countries which commonly use artesunate-amodiaquine or artesunate-mefloquine report fewer cases and deaths than those using artemether-lumefantrine or dihydroartemisinin-piperaquine. It could be necessary now to compare the antimalarial use and the dynamics of COVID-19 country by country to confirm this hypothesis.

DOI: 10.1016/j.tmaid.2020.101873
PubMed: 32916297
PubMed Central: PMC7477610

Links to Exploration step

pubmed:32916297

Le document en format XML

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<name sortKey="Le Bideau, Marion" sort="Le Bideau, Marion" uniqKey="Le Bideau M" first="Marion" last="Le Bideau">Marion Le Bideau</name>
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<nlm:affiliation>IHU Méditerranée Infection, Marseille, France; Aix Marseille Univ, IRD, AP-HM, MEPHI, Marseille, France.</nlm:affiliation>
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<name sortKey="Rolland, Clara" sort="Rolland, Clara" uniqKey="Rolland C" first="Clara" last="Rolland">Clara Rolland</name>
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<nlm:affiliation>Unité Parasitologie et Entomologie, Département Microbiologie et Maladies Infectieuses, Institut de Recherche Biomédicale des Armées, Marseille, France; Aix Marseille Univ, IRD, SSA, AP-HM, VITROME, Marseille, France; IHU Méditerranée Infection, Marseille, France; Centre National de Référence Du Paludisme, Marseille, France.</nlm:affiliation>
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<name sortKey="Hutter, Sebastien" sort="Hutter, Sebastien" uniqKey="Hutter S" first="Sébastien" last="Hutter">Sébastien Hutter</name>
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<nlm:affiliation>Aix Marseille Univ, IRD, SSA, AP-HM, VITROME, Marseille, France; IHU Méditerranée Infection, Marseille, France.</nlm:affiliation>
</affiliation>
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<name sortKey="La Scola, Bernard" sort="La Scola, Bernard" uniqKey="La Scola B" first="Bernard" last="La Scola">Bernard La Scola</name>
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<nlm:affiliation>IHU Méditerranée Infection, Marseille, France; Aix Marseille Univ, IRD, AP-HM, MEPHI, Marseille, France. Electronic address: bruno.pradines@gmail.com.</nlm:affiliation>
</affiliation>
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<nlm:affiliation>Unité Parasitologie et Entomologie, Département Microbiologie et Maladies Infectieuses, Institut de Recherche Biomédicale des Armées, Marseille, France; Aix Marseille Univ, IRD, SSA, AP-HM, VITROME, Marseille, France; IHU Méditerranée Infection, Marseille, France; Centre National de Référence Du Paludisme, Marseille, France. Electronic address: bernard.la-scola@univ-amu.fr.</nlm:affiliation>
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<term>Betacoronavirus (drug effects)</term>
<term>Cell Survival (drug effects)</term>
<term>Chlorocebus aethiops (MeSH)</term>
<term>SARS-CoV-2 (MeSH)</term>
<term>Vero Cells (MeSH)</term>
<term>Virus Replication (drug effects)</term>
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<term>Antimalarials</term>
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<term>Betacoronavirus</term>
<term>Cell Survival</term>
<term>Virus Replication</term>
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<div type="abstract" xml:lang="en">In December 2019, a new severe acute respiratory syndrome coronavirus (SARS-CoV-2) causing coronavirus diseases 2019 (COVID-19) emerged in Wuhan, China. African countries see slower dynamic of COVID-19 cases and deaths. One of the assumptions that may explain this later emergence in Africa, and more particularly in malaria endemic areas, would be the use of antimalarial drugs. We investigated the in vitro antiviral activity against SARS-CoV-2 of several antimalarial drugs. Chloroquine (EC
<sub>50</sub>
 = 2.1 μM and EC
<sub>90</sub>
 = 3.8 μM), hydroxychloroquine (EC
<sub>50</sub>
 = 1.5 μM and EC
<sub>90</sub>
 = 3.0 μM), ferroquine (EC
<sub>50</sub>
 = 1.5 μM and EC
<sub>90</sub>
 = 2.4 μM), desethylamodiaquine (EC
<sub>50</sub>
 = 0.52 μM and EC
<sub>90</sub>
 = 1.9 μM), mefloquine (EC
<sub>50</sub>
 = 1.8 μM and EC
<sub>90</sub>
 = 8.1 μM), pyronaridine (EC
<sub>50</sub>
 = 0.72 μM and EC
<sub>90</sub>
 = 0.75 μM) and quinine (EC
<sub>50</sub>
 = 10.7 μM and EC
<sub>90</sub>
 = 38.8 μM) showed in vitro antiviral effective activity with IC
<sub>50</sub>
and IC
<sub>90</sub>
compatible with drug oral uptake at doses commonly administered in malaria treatment. The ratio C
<sub>lung</sub>
/EC
<sub>90</sub>
ranged from 5 to 59. Lumefantrine, piperaquine and dihydroartemisinin had IC
<sub>50</sub>
and IC
<sub>90</sub>
too high to be compatible with expected plasma concentrations (ratio C
<sub>max</sub>
/EC
<sub>90</sub>
 < 0.05). Based on our results, we would expect that countries which commonly use artesunate-amodiaquine or artesunate-mefloquine report fewer cases and deaths than those using artemether-lumefantrine or dihydroartemisinin-piperaquine. It could be necessary now to compare the antimalarial use and the dynamics of COVID-19 country by country to confirm this hypothesis.</div>
</front>
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<AbstractText>In December 2019, a new severe acute respiratory syndrome coronavirus (SARS-CoV-2) causing coronavirus diseases 2019 (COVID-19) emerged in Wuhan, China. African countries see slower dynamic of COVID-19 cases and deaths. One of the assumptions that may explain this later emergence in Africa, and more particularly in malaria endemic areas, would be the use of antimalarial drugs. We investigated the in vitro antiviral activity against SARS-CoV-2 of several antimalarial drugs. Chloroquine (EC
<sub>50</sub>
 = 2.1 μM and EC
<sub>90</sub>
 = 3.8 μM), hydroxychloroquine (EC
<sub>50</sub>
 = 1.5 μM and EC
<sub>90</sub>
 = 3.0 μM), ferroquine (EC
<sub>50</sub>
 = 1.5 μM and EC
<sub>90</sub>
 = 2.4 μM), desethylamodiaquine (EC
<sub>50</sub>
 = 0.52 μM and EC
<sub>90</sub>
 = 1.9 μM), mefloquine (EC
<sub>50</sub>
 = 1.8 μM and EC
<sub>90</sub>
 = 8.1 μM), pyronaridine (EC
<sub>50</sub>
 = 0.72 μM and EC
<sub>90</sub>
 = 0.75 μM) and quinine (EC
<sub>50</sub>
 = 10.7 μM and EC
<sub>90</sub>
 = 38.8 μM) showed in vitro antiviral effective activity with IC
<sub>50</sub>
and IC
<sub>90</sub>
compatible with drug oral uptake at doses commonly administered in malaria treatment. The ratio C
<sub>lung</sub>
/EC
<sub>90</sub>
ranged from 5 to 59. Lumefantrine, piperaquine and dihydroartemisinin had IC
<sub>50</sub>
and IC
<sub>90</sub>
too high to be compatible with expected plasma concentrations (ratio C
<sub>max</sub>
/EC
<sub>90</sub>
 < 0.05). Based on our results, we would expect that countries which commonly use artesunate-amodiaquine or artesunate-mefloquine report fewer cases and deaths than those using artemether-lumefantrine or dihydroartemisinin-piperaquine. It could be necessary now to compare the antimalarial use and the dynamics of COVID-19 country by country to confirm this hypothesis.</AbstractText>
<CopyrightInformation>Copyright © 2020 Elsevier Ltd. All rights reserved.</CopyrightInformation>
</Abstract>
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<Affiliation>Unité Parasitologie et Entomologie, Département Microbiologie et Maladies Infectieuses, Institut de Recherche Biomédicale des Armées, Marseille, France; Aix Marseille Univ, IRD, SSA, AP-HM, VITROME, Marseille, France; IHU Méditerranée Infection, Marseille, France; Centre National de Référence Du Paludisme, Marseille, France.</Affiliation>
</AffiliationInfo>
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</AffiliationInfo>
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