TY - JOUR
T1 - In vitro efficacy of artemisinin-based treatments against SARS-CoV-2
AU - Zhou, Yuyong
AU - Gilmore, Kerry
AU - Ramirez, Santseharay
AU - Settels, Eva
AU - Gammeltoft, Karen A
AU - Pham, Long V
AU - Fahnøe, Ulrik
AU - Feng, Shan
AU - Offersgaard, Anna
AU - Trimpert, Jakob
AU - Bukh, Jens
AU - Osterrieder, Klaus
AU - Gottwein, Judith M
AU - Seeberger, Peter H
N1 - © 2021. The Author(s).
PY - 2021/12
Y1 - 2021/12
N2 - Effective and affordable treatments for patients suffering from coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), are needed. We report in vitro efficacy of Artemisia annua extracts as well as artemisinin, artesunate, and artemether against SARS-CoV-2. The latter two are approved active pharmaceutical ingredients of anti-malarial drugs. Concentration-response antiviral treatment assays, based on immunostaining of SARS-CoV-2 spike glycoprotein, revealed that treatment with all studied extracts and compounds inhibited SARS-CoV-2 infection of VeroE6 cells, human hepatoma Huh7.5 cells and human lung cancer A549-hACE2 cells, without obvious influence of the cell type on antiviral efficacy. In treatment assays, artesunate proved most potent (range of 50% effective concentrations (EC50) in different cell types: 7-12 µg/mL), followed by artemether (53-98 µg/mL), A. annua extracts (83-260 µg/mL) and artemisinin (151 to at least 208 µg/mL). The selectivity indices (SI), calculated based on treatment and cell viability assays, were mostly below 10 (range 2 to 54), suggesting a small therapeutic window. Time-of-addition experiments in A549-hACE2 cells revealed that artesunate targeted SARS-CoV-2 at the post-entry level. Peak plasma concentrations of artesunate exceeding EC50 values can be achieved. Clinical studies are required to further evaluate the utility of these compounds as COVID-19 treatment.
AB - Effective and affordable treatments for patients suffering from coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), are needed. We report in vitro efficacy of Artemisia annua extracts as well as artemisinin, artesunate, and artemether against SARS-CoV-2. The latter two are approved active pharmaceutical ingredients of anti-malarial drugs. Concentration-response antiviral treatment assays, based on immunostaining of SARS-CoV-2 spike glycoprotein, revealed that treatment with all studied extracts and compounds inhibited SARS-CoV-2 infection of VeroE6 cells, human hepatoma Huh7.5 cells and human lung cancer A549-hACE2 cells, without obvious influence of the cell type on antiviral efficacy. In treatment assays, artesunate proved most potent (range of 50% effective concentrations (EC50) in different cell types: 7-12 µg/mL), followed by artemether (53-98 µg/mL), A. annua extracts (83-260 µg/mL) and artemisinin (151 to at least 208 µg/mL). The selectivity indices (SI), calculated based on treatment and cell viability assays, were mostly below 10 (range 2 to 54), suggesting a small therapeutic window. Time-of-addition experiments in A549-hACE2 cells revealed that artesunate targeted SARS-CoV-2 at the post-entry level. Peak plasma concentrations of artesunate exceeding EC50 values can be achieved. Clinical studies are required to further evaluate the utility of these compounds as COVID-19 treatment.
KW - A549 Cells
KW - Animals
KW - Artemisia annua/chemistry
KW - Artemisinins/pharmacology
KW - COVID-19/drug therapy
KW - Chlorocebus aethiops
KW - Humans
KW - Plant Extracts/pharmacology
KW - SARS-CoV-2/drug effects
KW - Vero Cells
UR - https://www.scopus.com/pages/publications/85109999065
U2 - 10.1038/s41598-021-93361-y
DO - 10.1038/s41598-021-93361-y
M3 - Journal article
C2 - 34272426
SN - 2045-2322
VL - 11
SP - 1
EP - 14
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 14571
ER -