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Treatment of SARS with human interferons

Effective antiviral agents are needed to treat severe acute respiratory syndrome-associated coronavirus (SARS-CoV) infection. We assessed the antiviral potential of recombinant interferons against two clinical isolates of SARS-CoV—FFM-1, from Frankfurt patients, and Hong Kong—replicated in Vero and...

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Autores principales: Cinatl, J, Morgenstern, B, Bauer, G, Chandra, P, Rabenau, H, Doerr, HW
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112413/
https://www.ncbi.nlm.nih.gov/pubmed/12892961
http://dx.doi.org/10.1016/S0140-6736(03)13973-6
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author Cinatl, J
Morgenstern, B
Bauer, G
Chandra, P
Rabenau, H
Doerr, HW
author_facet Cinatl, J
Morgenstern, B
Bauer, G
Chandra, P
Rabenau, H
Doerr, HW
author_sort Cinatl, J
collection PubMed
description Effective antiviral agents are needed to treat severe acute respiratory syndrome-associated coronavirus (SARS-CoV) infection. We assessed the antiviral potential of recombinant interferons against two clinical isolates of SARS-CoV—FFM-1, from Frankfurt patients, and Hong Kong—replicated in Vero and Caco2 cells. Interferon β was five to ten times more effective in Caco2 cells. Interferon α effectively inhibited SARS-CoV replication, but with a selectivity index 50–90 times lower than that for interferon β. Interferon γ was slightly better than interferon α in Vero cell cultures, but was completely ineffective in Caco2 cell cultures. Interferon β could be useful alone or in combination with other antiviral drugs for the treatment of SARS.
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spelling pubmed-71124132020-04-02 Treatment of SARS with human interferons Cinatl, J Morgenstern, B Bauer, G Chandra, P Rabenau, H Doerr, HW Lancet Fast track — Research Letters Effective antiviral agents are needed to treat severe acute respiratory syndrome-associated coronavirus (SARS-CoV) infection. We assessed the antiviral potential of recombinant interferons against two clinical isolates of SARS-CoV—FFM-1, from Frankfurt patients, and Hong Kong—replicated in Vero and Caco2 cells. Interferon β was five to ten times more effective in Caco2 cells. Interferon α effectively inhibited SARS-CoV replication, but with a selectivity index 50–90 times lower than that for interferon β. Interferon γ was slightly better than interferon α in Vero cell cultures, but was completely ineffective in Caco2 cell cultures. Interferon β could be useful alone or in combination with other antiviral drugs for the treatment of SARS. Elsevier Ltd. 2003-07-26 2003-07-24 /pmc/articles/PMC7112413/ /pubmed/12892961 http://dx.doi.org/10.1016/S0140-6736(03)13973-6 Text en Copyright © 2003 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Fast track — Research Letters
Cinatl, J
Morgenstern, B
Bauer, G
Chandra, P
Rabenau, H
Doerr, HW
Treatment of SARS with human interferons
title Treatment of SARS with human interferons
title_full Treatment of SARS with human interferons
title_fullStr Treatment of SARS with human interferons
title_full_unstemmed Treatment of SARS with human interferons
title_short Treatment of SARS with human interferons
title_sort treatment of sars with human interferons
topic Fast track — Research Letters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112413/
https://www.ncbi.nlm.nih.gov/pubmed/12892961
http://dx.doi.org/10.1016/S0140-6736(03)13973-6
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