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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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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