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Combination Chemotherapy for Influenza

The emergence of pandemic H1N1 influenza viruses in April 2009 and the continuous evolution of highly pathogenic H5N1 influenza viruses underscore the urgency of novel approaches to chemotherapy for human influenza infection. Anti-influenza drugs are currently limited to the neuraminidase inhibitors...

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Detalles Bibliográficos
Autores principales: Govorkova, Elena A., Webster, Robert G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185732/
https://www.ncbi.nlm.nih.gov/pubmed/21994692
http://dx.doi.org/10.3390/v2081510
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author Govorkova, Elena A.
Webster, Robert G.
author_facet Govorkova, Elena A.
Webster, Robert G.
author_sort Govorkova, Elena A.
collection PubMed
description The emergence of pandemic H1N1 influenza viruses in April 2009 and the continuous evolution of highly pathogenic H5N1 influenza viruses underscore the urgency of novel approaches to chemotherapy for human influenza infection. Anti-influenza drugs are currently limited to the neuraminidase inhibitors (oseltamivir and zanamivir) and to M2 ion channel blockers (amantadine and rimantadine), although resistance to the latter class develops rapidly. Potential targets for the development of new anti-influenza agents include the viral polymerase (and endonuclease), the hemagglutinin, and the non-structural protein NS1. The limitations of monotherapy and the emergence of drug-resistant variants make combination chemotherapy the logical therapeutic option. Here we review the experimental data on combination chemotherapy with currently available agents and the development of new agents and therapy targets.
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spelling pubmed-31857322011-10-12 Combination Chemotherapy for Influenza Govorkova, Elena A. Webster, Robert G. Viruses Review The emergence of pandemic H1N1 influenza viruses in April 2009 and the continuous evolution of highly pathogenic H5N1 influenza viruses underscore the urgency of novel approaches to chemotherapy for human influenza infection. Anti-influenza drugs are currently limited to the neuraminidase inhibitors (oseltamivir and zanamivir) and to M2 ion channel blockers (amantadine and rimantadine), although resistance to the latter class develops rapidly. Potential targets for the development of new anti-influenza agents include the viral polymerase (and endonuclease), the hemagglutinin, and the non-structural protein NS1. The limitations of monotherapy and the emergence of drug-resistant variants make combination chemotherapy the logical therapeutic option. Here we review the experimental data on combination chemotherapy with currently available agents and the development of new agents and therapy targets. Molecular Diversity Preservation International (MDPI) 2010-07-27 /pmc/articles/PMC3185732/ /pubmed/21994692 http://dx.doi.org/10.3390/v2081510 Text en © 2010 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Govorkova, Elena A.
Webster, Robert G.
Combination Chemotherapy for Influenza
title Combination Chemotherapy for Influenza
title_full Combination Chemotherapy for Influenza
title_fullStr Combination Chemotherapy for Influenza
title_full_unstemmed Combination Chemotherapy for Influenza
title_short Combination Chemotherapy for Influenza
title_sort combination chemotherapy for influenza
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185732/
https://www.ncbi.nlm.nih.gov/pubmed/21994692
http://dx.doi.org/10.3390/v2081510
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