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Antiviral combinations for severe influenza
Observational data suggest that the treatment of influenza infection with neuraminidase inhibitors decreases progression to more severe illness, especially when treatment is started soon after symptom onset. However, even early treatment might fail to prevent complications in some patients, particul...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164787/ https://www.ncbi.nlm.nih.gov/pubmed/25213733 http://dx.doi.org/10.1016/S1473-3099(14)70821-7 |
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author | Dunning, Jake Baillie, J Kenneth Cao, Bin Hayden, Frederick G |
author_facet | Dunning, Jake Baillie, J Kenneth Cao, Bin Hayden, Frederick G |
author_sort | Dunning, Jake |
collection | PubMed |
description | Observational data suggest that the treatment of influenza infection with neuraminidase inhibitors decreases progression to more severe illness, especially when treatment is started soon after symptom onset. However, even early treatment might fail to prevent complications in some patients, particularly those infected with novel viruses such as the 2009 pandemic influenza A H1N1, avian influenza A H5N1 virus subtype, or the avian influenza A H7N9 virus subtype. Furthermore, treatment with one antiviral drug might promote the development of antiviral resistance, especially in immunocompromised hosts and critically ill patients. An obvious strategy to optimise antiviral therapy is to combine drugs with different modes of action. Because host immune responses to infection might also contribute to illness pathogenesis, improved outcomes might be gained from the combination of antiviral therapy with drugs that modulate the immune response in an infected individual. We review available data from preclinical and clinical studies of combination antiviral therapy and of combined antiviral-immunomodulator therapy for influenza. Early-stage data draw attention to several promising antiviral combinations with therapeutic potential in severe infections, but there remains a need to substantiate clinical benefit. Combination therapies with favourable experimental data need to be tested in carefully designed aclinical trials to assess their efficacy. |
format | Online Article Text |
id | pubmed-7164787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71647872020-04-20 Antiviral combinations for severe influenza Dunning, Jake Baillie, J Kenneth Cao, Bin Hayden, Frederick G Lancet Infect Dis Article Observational data suggest that the treatment of influenza infection with neuraminidase inhibitors decreases progression to more severe illness, especially when treatment is started soon after symptom onset. However, even early treatment might fail to prevent complications in some patients, particularly those infected with novel viruses such as the 2009 pandemic influenza A H1N1, avian influenza A H5N1 virus subtype, or the avian influenza A H7N9 virus subtype. Furthermore, treatment with one antiviral drug might promote the development of antiviral resistance, especially in immunocompromised hosts and critically ill patients. An obvious strategy to optimise antiviral therapy is to combine drugs with different modes of action. Because host immune responses to infection might also contribute to illness pathogenesis, improved outcomes might be gained from the combination of antiviral therapy with drugs that modulate the immune response in an infected individual. We review available data from preclinical and clinical studies of combination antiviral therapy and of combined antiviral-immunomodulator therapy for influenza. Early-stage data draw attention to several promising antiviral combinations with therapeutic potential in severe infections, but there remains a need to substantiate clinical benefit. Combination therapies with favourable experimental data need to be tested in carefully designed aclinical trials to assess their efficacy. Elsevier Ltd. 2014-12 2014-09-08 /pmc/articles/PMC7164787/ /pubmed/25213733 http://dx.doi.org/10.1016/S1473-3099(14)70821-7 Text en Copyright © 2014 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 | Article Dunning, Jake Baillie, J Kenneth Cao, Bin Hayden, Frederick G Antiviral combinations for severe influenza |
title | Antiviral combinations for severe influenza |
title_full | Antiviral combinations for severe influenza |
title_fullStr | Antiviral combinations for severe influenza |
title_full_unstemmed | Antiviral combinations for severe influenza |
title_short | Antiviral combinations for severe influenza |
title_sort | antiviral combinations for severe influenza |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164787/ https://www.ncbi.nlm.nih.gov/pubmed/25213733 http://dx.doi.org/10.1016/S1473-3099(14)70821-7 |
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