Perspectives for antivirals to limit SARS-CoV-2 infection (COVID-19)

Compared with vaccines, antivirals for curbing COVID-19 (SARS-CoV-2 infection) have been developed at a much lower pace. Favipiravir has proven efficacious (in hamsters) but only at a very high dose which may not be feasible in humans. Remdesivir is the sole antiviral approved by the US FDA, but it...

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Main Author: Erik De Clercq
Format: Article
Language:English
Published: CSIRO Publishing 2021-01-01
Series:Microbiology Australia
Online Access:https://www.publish.csiro.au/ma/pdf/MA21013
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spelling doaj-d6e01acb52cc471eb72634dd93ada1c92021-05-26T03:34:04ZengCSIRO PublishingMicrobiology Australia1324-42722201-91892021-01-014214753MA21013Perspectives for antivirals to limit SARS-CoV-2 infection (COVID-19)Erik De Clercq0KU Leuven, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, Herestraat 49, 3000 Leuven, Belgium. Tel.: + 32 16 37 90 20; Email: erik.declercq@kuleuven.beCompared with vaccines, antivirals for curbing COVID-19 (SARS-CoV-2 infection) have been developed at a much lower pace. Favipiravir has proven efficacious (in hamsters) but only at a very high dose which may not be feasible in humans. Remdesivir is the sole antiviral approved by the US FDA, but it has not been extensively evaluated for its safety. EIDD-1931 and EIDD-2801 have not been evaluated clinically. Mpro (protease) inhibitors likewise need to be subjected to clinical efficacy and safety studies. Remdesivir is a C-nucleoside and this class of compounds should be further evaluated. Polyanionic substances interfering with virus adsorption to the host cells have not been explored. They may possibly be administered by inhalation. Corticosteroids (such as dexamethasone), while virus-stimulating rather than inhibitory, may counteract the ‘cytokine storm’. Combination of (two or more of) the compounds mentioned above may offer an increased benefit through a synergistic interaction.https://www.publish.csiro.au/ma/pdf/MA21013
collection DOAJ
language English
format Article
sources DOAJ
author Erik De Clercq
spellingShingle Erik De Clercq
Perspectives for antivirals to limit SARS-CoV-2 infection (COVID-19)
Microbiology Australia
author_facet Erik De Clercq
author_sort Erik De Clercq
title Perspectives for antivirals to limit SARS-CoV-2 infection (COVID-19)
title_short Perspectives for antivirals to limit SARS-CoV-2 infection (COVID-19)
title_full Perspectives for antivirals to limit SARS-CoV-2 infection (COVID-19)
title_fullStr Perspectives for antivirals to limit SARS-CoV-2 infection (COVID-19)
title_full_unstemmed Perspectives for antivirals to limit SARS-CoV-2 infection (COVID-19)
title_sort perspectives for antivirals to limit sars-cov-2 infection (covid-19)
publisher CSIRO Publishing
series Microbiology Australia
issn 1324-4272
2201-9189
publishDate 2021-01-01
description Compared with vaccines, antivirals for curbing COVID-19 (SARS-CoV-2 infection) have been developed at a much lower pace. Favipiravir has proven efficacious (in hamsters) but only at a very high dose which may not be feasible in humans. Remdesivir is the sole antiviral approved by the US FDA, but it has not been extensively evaluated for its safety. EIDD-1931 and EIDD-2801 have not been evaluated clinically. Mpro (protease) inhibitors likewise need to be subjected to clinical efficacy and safety studies. Remdesivir is a C-nucleoside and this class of compounds should be further evaluated. Polyanionic substances interfering with virus adsorption to the host cells have not been explored. They may possibly be administered by inhalation. Corticosteroids (such as dexamethasone), while virus-stimulating rather than inhibitory, may counteract the ‘cytokine storm’. Combination of (two or more of) the compounds mentioned above may offer an increased benefit through a synergistic interaction.
url https://www.publish.csiro.au/ma/pdf/MA21013
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