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Mefloquine, a Potent Anti-severe Acute Respiratory Syndrome-Related Coronavirus 2 (SARS-CoV-2) Drug as an Entry Inhibitor in vitro
Coronavirus disease 2019 (COVID-19) has caused serious public health, social, and economic damage worldwide and effective drugs that prevent or cure COVID-19 are urgently needed. Approved drugs including Hydroxychloroquine, Remdesivir or Interferon were reported to inhibit the infection or propagati...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119653/ https://www.ncbi.nlm.nih.gov/pubmed/33995308 http://dx.doi.org/10.3389/fmicb.2021.651403 |
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author | Shionoya, Kaho Yamasaki, Masako Iwanami, Shoya Ito, Yusuke Fukushi, Shuetsu Ohashi, Hirofumi Saso, Wakana Tanaka, Tomohiro Aoki, Shin Kuramochi, Kouji Iwami, Shingo Takahashi, Yoshimasa Suzuki, Tadaki Muramatsu, Masamichi Takeda, Makoto Wakita, Takaji Watashi, Koichi |
author_facet | Shionoya, Kaho Yamasaki, Masako Iwanami, Shoya Ito, Yusuke Fukushi, Shuetsu Ohashi, Hirofumi Saso, Wakana Tanaka, Tomohiro Aoki, Shin Kuramochi, Kouji Iwami, Shingo Takahashi, Yoshimasa Suzuki, Tadaki Muramatsu, Masamichi Takeda, Makoto Wakita, Takaji Watashi, Koichi |
author_sort | Shionoya, Kaho |
collection | PubMed |
description | Coronavirus disease 2019 (COVID-19) has caused serious public health, social, and economic damage worldwide and effective drugs that prevent or cure COVID-19 are urgently needed. Approved drugs including Hydroxychloroquine, Remdesivir or Interferon were reported to inhibit the infection or propagation of severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2), however, their clinical efficacies have not yet been well demonstrated. To identify drugs with higher antiviral potency, we screened approved anti-parasitic/anti-protozoal drugs and identified an anti-malarial drug, Mefloquine, which showed the highest anti-SARS-CoV-2 activity among the tested compounds. Mefloquine showed higher anti-SARS-CoV-2 activity than Hydroxychloroquine in VeroE6/TMPRSS2 and Calu-3 cells, with IC(50) = 1.28 μM, IC(90) = 2.31 μM, and IC(99) = 4.39 μM in VeroE6/TMPRSS2 cells. Mefloquine inhibited viral entry after viral attachment to the target cell. Combined treatment with Mefloquine and Nelfinavir, a replication inhibitor, showed synergistic antiviral activity. Our mathematical modeling based on the drug concentration in the lung predicted that Mefloquine administration at a standard treatment dosage could decline viral dynamics in patients, reduce cumulative viral load to 7% and shorten the time until virus elimination by 6.1 days. These data cumulatively underscore Mefloquine as an anti-SARS-CoV-2 entry inhibitor. |
format | Online Article Text |
id | pubmed-8119653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81196532021-05-15 Mefloquine, a Potent Anti-severe Acute Respiratory Syndrome-Related Coronavirus 2 (SARS-CoV-2) Drug as an Entry Inhibitor in vitro Shionoya, Kaho Yamasaki, Masako Iwanami, Shoya Ito, Yusuke Fukushi, Shuetsu Ohashi, Hirofumi Saso, Wakana Tanaka, Tomohiro Aoki, Shin Kuramochi, Kouji Iwami, Shingo Takahashi, Yoshimasa Suzuki, Tadaki Muramatsu, Masamichi Takeda, Makoto Wakita, Takaji Watashi, Koichi Front Microbiol Microbiology Coronavirus disease 2019 (COVID-19) has caused serious public health, social, and economic damage worldwide and effective drugs that prevent or cure COVID-19 are urgently needed. Approved drugs including Hydroxychloroquine, Remdesivir or Interferon were reported to inhibit the infection or propagation of severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2), however, their clinical efficacies have not yet been well demonstrated. To identify drugs with higher antiviral potency, we screened approved anti-parasitic/anti-protozoal drugs and identified an anti-malarial drug, Mefloquine, which showed the highest anti-SARS-CoV-2 activity among the tested compounds. Mefloquine showed higher anti-SARS-CoV-2 activity than Hydroxychloroquine in VeroE6/TMPRSS2 and Calu-3 cells, with IC(50) = 1.28 μM, IC(90) = 2.31 μM, and IC(99) = 4.39 μM in VeroE6/TMPRSS2 cells. Mefloquine inhibited viral entry after viral attachment to the target cell. Combined treatment with Mefloquine and Nelfinavir, a replication inhibitor, showed synergistic antiviral activity. Our mathematical modeling based on the drug concentration in the lung predicted that Mefloquine administration at a standard treatment dosage could decline viral dynamics in patients, reduce cumulative viral load to 7% and shorten the time until virus elimination by 6.1 days. These data cumulatively underscore Mefloquine as an anti-SARS-CoV-2 entry inhibitor. Frontiers Media S.A. 2021-04-30 /pmc/articles/PMC8119653/ /pubmed/33995308 http://dx.doi.org/10.3389/fmicb.2021.651403 Text en Copyright © 2021 Shionoya, Yamasaki, Iwanami, Ito, Fukushi, Ohashi, Saso, Tanaka, Aoki, Kuramochi, Iwami, Takahashi, Suzuki, Muramatsu, Takeda, Wakita and Watashi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Shionoya, Kaho Yamasaki, Masako Iwanami, Shoya Ito, Yusuke Fukushi, Shuetsu Ohashi, Hirofumi Saso, Wakana Tanaka, Tomohiro Aoki, Shin Kuramochi, Kouji Iwami, Shingo Takahashi, Yoshimasa Suzuki, Tadaki Muramatsu, Masamichi Takeda, Makoto Wakita, Takaji Watashi, Koichi Mefloquine, a Potent Anti-severe Acute Respiratory Syndrome-Related Coronavirus 2 (SARS-CoV-2) Drug as an Entry Inhibitor in vitro |
title | Mefloquine, a Potent Anti-severe Acute Respiratory Syndrome-Related Coronavirus 2 (SARS-CoV-2) Drug as an Entry Inhibitor in vitro |
title_full | Mefloquine, a Potent Anti-severe Acute Respiratory Syndrome-Related Coronavirus 2 (SARS-CoV-2) Drug as an Entry Inhibitor in vitro |
title_fullStr | Mefloquine, a Potent Anti-severe Acute Respiratory Syndrome-Related Coronavirus 2 (SARS-CoV-2) Drug as an Entry Inhibitor in vitro |
title_full_unstemmed | Mefloquine, a Potent Anti-severe Acute Respiratory Syndrome-Related Coronavirus 2 (SARS-CoV-2) Drug as an Entry Inhibitor in vitro |
title_short | Mefloquine, a Potent Anti-severe Acute Respiratory Syndrome-Related Coronavirus 2 (SARS-CoV-2) Drug as an Entry Inhibitor in vitro |
title_sort | mefloquine, a potent anti-severe acute respiratory syndrome-related coronavirus 2 (sars-cov-2) drug as an entry inhibitor in vitro |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119653/ https://www.ncbi.nlm.nih.gov/pubmed/33995308 http://dx.doi.org/10.3389/fmicb.2021.651403 |
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