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Protection from pulmonary tissue damage associated with infection of cynomolgus macaques by highly pathogenic avian influenza virus (H5N1) by low dose natural human IFN-α administered to the buccal mucosa

Using an established nonhuman primate model for H5N1 highly pathogenic influenza virus infection in humans, we have been able to demonstrate the prophylactic mitigation of the pulmonary damage characteristic of human fatal cases from primary influenza virus pneumonia with a low dose oral formulation...

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Autores principales: Strayer, David R., Carter, William A., Stouch, Bruce C., Stittelaar, Koert J., Thoolen, Robert J.M.M., Osterhaus, Albert D.M.E., Mitchell, William M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier B.V. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113766/
https://www.ncbi.nlm.nih.gov/pubmed/25111905
http://dx.doi.org/10.1016/j.antiviral.2014.07.010
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author Strayer, David R.
Carter, William A.
Stouch, Bruce C.
Stittelaar, Koert J.
Thoolen, Robert J.M.M.
Osterhaus, Albert D.M.E.
Mitchell, William M.
author_facet Strayer, David R.
Carter, William A.
Stouch, Bruce C.
Stittelaar, Koert J.
Thoolen, Robert J.M.M.
Osterhaus, Albert D.M.E.
Mitchell, William M.
author_sort Strayer, David R.
collection PubMed
description Using an established nonhuman primate model for H5N1 highly pathogenic influenza virus infection in humans, we have been able to demonstrate the prophylactic mitigation of the pulmonary damage characteristic of human fatal cases from primary influenza virus pneumonia with a low dose oral formulation of a commercially available parenteral natural human interferon alpha (Alferon N Injection®). At the highest oral dose (62.5 IU/kg body weight) used there was a marked reduction in the alveolar inflammatory response with minor evidence of alveolar and interstitial edema in contrast to the hemorrhage and inflammatory response observed in the alveoli of control animals. The mitigation of severe damage to the lower pulmonary airway was observed without a parallel reduction in viral titers. Clinical trial data will be necessary to establish its prophylactic human efficacy for highly pathogenic influenza viruses.
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spelling pubmed-71137662020-04-02 Protection from pulmonary tissue damage associated with infection of cynomolgus macaques by highly pathogenic avian influenza virus (H5N1) by low dose natural human IFN-α administered to the buccal mucosa Strayer, David R. Carter, William A. Stouch, Bruce C. Stittelaar, Koert J. Thoolen, Robert J.M.M. Osterhaus, Albert D.M.E. Mitchell, William M. Antiviral Res Article Using an established nonhuman primate model for H5N1 highly pathogenic influenza virus infection in humans, we have been able to demonstrate the prophylactic mitigation of the pulmonary damage characteristic of human fatal cases from primary influenza virus pneumonia with a low dose oral formulation of a commercially available parenteral natural human interferon alpha (Alferon N Injection®). At the highest oral dose (62.5 IU/kg body weight) used there was a marked reduction in the alveolar inflammatory response with minor evidence of alveolar and interstitial edema in contrast to the hemorrhage and inflammatory response observed in the alveoli of control animals. The mitigation of severe damage to the lower pulmonary airway was observed without a parallel reduction in viral titers. Clinical trial data will be necessary to establish its prophylactic human efficacy for highly pathogenic influenza viruses. Published by Elsevier B.V. 2014-10 2014-08-09 /pmc/articles/PMC7113766/ /pubmed/25111905 http://dx.doi.org/10.1016/j.antiviral.2014.07.010 Text en Copyright © 2014 Published by Elsevier B.V. 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
Strayer, David R.
Carter, William A.
Stouch, Bruce C.
Stittelaar, Koert J.
Thoolen, Robert J.M.M.
Osterhaus, Albert D.M.E.
Mitchell, William M.
Protection from pulmonary tissue damage associated with infection of cynomolgus macaques by highly pathogenic avian influenza virus (H5N1) by low dose natural human IFN-α administered to the buccal mucosa
title Protection from pulmonary tissue damage associated with infection of cynomolgus macaques by highly pathogenic avian influenza virus (H5N1) by low dose natural human IFN-α administered to the buccal mucosa
title_full Protection from pulmonary tissue damage associated with infection of cynomolgus macaques by highly pathogenic avian influenza virus (H5N1) by low dose natural human IFN-α administered to the buccal mucosa
title_fullStr Protection from pulmonary tissue damage associated with infection of cynomolgus macaques by highly pathogenic avian influenza virus (H5N1) by low dose natural human IFN-α administered to the buccal mucosa
title_full_unstemmed Protection from pulmonary tissue damage associated with infection of cynomolgus macaques by highly pathogenic avian influenza virus (H5N1) by low dose natural human IFN-α administered to the buccal mucosa
title_short Protection from pulmonary tissue damage associated with infection of cynomolgus macaques by highly pathogenic avian influenza virus (H5N1) by low dose natural human IFN-α administered to the buccal mucosa
title_sort protection from pulmonary tissue damage associated with infection of cynomolgus macaques by highly pathogenic avian influenza virus (h5n1) by low dose natural human ifn-α administered to the buccal mucosa
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113766/
https://www.ncbi.nlm.nih.gov/pubmed/25111905
http://dx.doi.org/10.1016/j.antiviral.2014.07.010
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