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The role of adjuvant immunomodulatory agents for treatment of severe influenza

A severe inflammatory immune response with hypercytokinemia occurs in patients hospitalized with severe influenza, such as avian influenza A(H5N1), A(H7N9), and seasonal A(H1N1)pdm09 virus infections. The role of immunomodulatory therapy is unclear as there have been limited published data based on...

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Autores principales: Hui, David S., Lee, Nelson, Chan, Paul K., Beigel, John H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801167/
https://www.ncbi.nlm.nih.gov/pubmed/29325970
http://dx.doi.org/10.1016/j.antiviral.2018.01.002
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author Hui, David S.
Lee, Nelson
Chan, Paul K.
Beigel, John H.
author_facet Hui, David S.
Lee, Nelson
Chan, Paul K.
Beigel, John H.
author_sort Hui, David S.
collection PubMed
description A severe inflammatory immune response with hypercytokinemia occurs in patients hospitalized with severe influenza, such as avian influenza A(H5N1), A(H7N9), and seasonal A(H1N1)pdm09 virus infections. The role of immunomodulatory therapy is unclear as there have been limited published data based on randomized controlled trials (RCTs). Passive immunotherapy such as convalescent plasma and hyperimmune globulin have some studies demonstrating benefit when administered as an adjunctive therapy for severe influenza. Triple combination of oseltamivir, clarithromycin, and naproxen for severe influenza has one study supporting its use, and confirmatory studies would be of great interest. Likewise, confirmatory studies of sirolimus without concomitant corticosteroid therapy should be explored as a research priority. Other agents with potential immunomodulating effects, including non-immune intravenous immunoglobulin, N-acetylcysteine, acute use of statins, macrolides, pamidronate, nitazoxanide, chloroquine, antiC5a antibody, interferons, human mesenchymal stromal cells, mycophenolic acid, peroxisome proliferator-activated receptors agonists, non-steroidal anti-inflammatory agents, mesalazine, herbal medicine, and the role of plasmapheresis and hemoperfusion as rescue therapy have supportive preclinical or observational clinical data, and deserve more investigation preferably by RCTs. Systemic corticosteroids administered in high dose may increase the risk of mortality and morbidity in patients with severe influenza and should not be used, while the clinical utility of low dose systemic corticosteroids requires further investigation.
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spelling pubmed-58011672019-02-01 The role of adjuvant immunomodulatory agents for treatment of severe influenza Hui, David S. Lee, Nelson Chan, Paul K. Beigel, John H. Antiviral Res Review Article A severe inflammatory immune response with hypercytokinemia occurs in patients hospitalized with severe influenza, such as avian influenza A(H5N1), A(H7N9), and seasonal A(H1N1)pdm09 virus infections. The role of immunomodulatory therapy is unclear as there have been limited published data based on randomized controlled trials (RCTs). Passive immunotherapy such as convalescent plasma and hyperimmune globulin have some studies demonstrating benefit when administered as an adjunctive therapy for severe influenza. Triple combination of oseltamivir, clarithromycin, and naproxen for severe influenza has one study supporting its use, and confirmatory studies would be of great interest. Likewise, confirmatory studies of sirolimus without concomitant corticosteroid therapy should be explored as a research priority. Other agents with potential immunomodulating effects, including non-immune intravenous immunoglobulin, N-acetylcysteine, acute use of statins, macrolides, pamidronate, nitazoxanide, chloroquine, antiC5a antibody, interferons, human mesenchymal stromal cells, mycophenolic acid, peroxisome proliferator-activated receptors agonists, non-steroidal anti-inflammatory agents, mesalazine, herbal medicine, and the role of plasmapheresis and hemoperfusion as rescue therapy have supportive preclinical or observational clinical data, and deserve more investigation preferably by RCTs. Systemic corticosteroids administered in high dose may increase the risk of mortality and morbidity in patients with severe influenza and should not be used, while the clinical utility of low dose systemic corticosteroids requires further investigation. Elsevier B.V. 2018-02 2018-01-08 /pmc/articles/PMC5801167/ /pubmed/29325970 http://dx.doi.org/10.1016/j.antiviral.2018.01.002 Text en © 2018 Elsevier B.V. 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 Review Article
Hui, David S.
Lee, Nelson
Chan, Paul K.
Beigel, John H.
The role of adjuvant immunomodulatory agents for treatment of severe influenza
title The role of adjuvant immunomodulatory agents for treatment of severe influenza
title_full The role of adjuvant immunomodulatory agents for treatment of severe influenza
title_fullStr The role of adjuvant immunomodulatory agents for treatment of severe influenza
title_full_unstemmed The role of adjuvant immunomodulatory agents for treatment of severe influenza
title_short The role of adjuvant immunomodulatory agents for treatment of severe influenza
title_sort role of adjuvant immunomodulatory agents for treatment of severe influenza
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801167/
https://www.ncbi.nlm.nih.gov/pubmed/29325970
http://dx.doi.org/10.1016/j.antiviral.2018.01.002
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