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Suppressor of cytokine signaling (SOCS)5 ameliorates influenza infection via inhibition of EGFR signaling
Influenza virus infections have a significant impact on global human health. Individuals with suppressed immunity, or suffering from chronic inflammatory conditions such as COPD, are particularly susceptible to influenza. Here we show that suppressor of cytokine signaling (SOCS) five has a pivotal r...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354519/ https://www.ncbi.nlm.nih.gov/pubmed/28195529 http://dx.doi.org/10.7554/eLife.20444 |
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author | Kedzierski, Lukasz Tate, Michelle D Hsu, Alan C Kolesnik, Tatiana B Linossi, Edmond M Dagley, Laura Dong, Zhaoguang Freeman, Sarah Infusini, Giuseppe Starkey, Malcolm R Bird, Nicola L Chatfield, Simon M Babon, Jeffrey J Huntington, Nicholas Belz, Gabrielle Webb, Andrew Wark, Peter AB Nicola, Nicos A Xu, Jianqing Kedzierska, Katherine Hansbro, Philip M Nicholson, Sandra E |
author_facet | Kedzierski, Lukasz Tate, Michelle D Hsu, Alan C Kolesnik, Tatiana B Linossi, Edmond M Dagley, Laura Dong, Zhaoguang Freeman, Sarah Infusini, Giuseppe Starkey, Malcolm R Bird, Nicola L Chatfield, Simon M Babon, Jeffrey J Huntington, Nicholas Belz, Gabrielle Webb, Andrew Wark, Peter AB Nicola, Nicos A Xu, Jianqing Kedzierska, Katherine Hansbro, Philip M Nicholson, Sandra E |
author_sort | Kedzierski, Lukasz |
collection | PubMed |
description | Influenza virus infections have a significant impact on global human health. Individuals with suppressed immunity, or suffering from chronic inflammatory conditions such as COPD, are particularly susceptible to influenza. Here we show that suppressor of cytokine signaling (SOCS) five has a pivotal role in restricting influenza A virus in the airway epithelium, through the regulation of epidermal growth factor receptor (EGFR). Socs5-deficient mice exhibit heightened disease severity, with increased viral titres and weight loss. Socs5 levels were differentially regulated in response to distinct influenza viruses (H1N1, H3N2, H5N1 and H11N9) and were reduced in primary epithelial cells from COPD patients, again correlating with increased susceptibility to influenza. Importantly, restoration of SOCS5 levels restricted influenza virus infection, suggesting that manipulating SOCS5 expression and/or SOCS5 targets might be a novel therapeutic approach to influenza. DOI: http://dx.doi.org/10.7554/eLife.20444.001 |
format | Online Article Text |
id | pubmed-5354519 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53545192017-03-17 Suppressor of cytokine signaling (SOCS)5 ameliorates influenza infection via inhibition of EGFR signaling Kedzierski, Lukasz Tate, Michelle D Hsu, Alan C Kolesnik, Tatiana B Linossi, Edmond M Dagley, Laura Dong, Zhaoguang Freeman, Sarah Infusini, Giuseppe Starkey, Malcolm R Bird, Nicola L Chatfield, Simon M Babon, Jeffrey J Huntington, Nicholas Belz, Gabrielle Webb, Andrew Wark, Peter AB Nicola, Nicos A Xu, Jianqing Kedzierska, Katherine Hansbro, Philip M Nicholson, Sandra E eLife Cell Biology Influenza virus infections have a significant impact on global human health. Individuals with suppressed immunity, or suffering from chronic inflammatory conditions such as COPD, are particularly susceptible to influenza. Here we show that suppressor of cytokine signaling (SOCS) five has a pivotal role in restricting influenza A virus in the airway epithelium, through the regulation of epidermal growth factor receptor (EGFR). Socs5-deficient mice exhibit heightened disease severity, with increased viral titres and weight loss. Socs5 levels were differentially regulated in response to distinct influenza viruses (H1N1, H3N2, H5N1 and H11N9) and were reduced in primary epithelial cells from COPD patients, again correlating with increased susceptibility to influenza. Importantly, restoration of SOCS5 levels restricted influenza virus infection, suggesting that manipulating SOCS5 expression and/or SOCS5 targets might be a novel therapeutic approach to influenza. DOI: http://dx.doi.org/10.7554/eLife.20444.001 eLife Sciences Publications, Ltd 2017-02-14 /pmc/articles/PMC5354519/ /pubmed/28195529 http://dx.doi.org/10.7554/eLife.20444 Text en © 2017, Kedzierski et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Kedzierski, Lukasz Tate, Michelle D Hsu, Alan C Kolesnik, Tatiana B Linossi, Edmond M Dagley, Laura Dong, Zhaoguang Freeman, Sarah Infusini, Giuseppe Starkey, Malcolm R Bird, Nicola L Chatfield, Simon M Babon, Jeffrey J Huntington, Nicholas Belz, Gabrielle Webb, Andrew Wark, Peter AB Nicola, Nicos A Xu, Jianqing Kedzierska, Katherine Hansbro, Philip M Nicholson, Sandra E Suppressor of cytokine signaling (SOCS)5 ameliorates influenza infection via inhibition of EGFR signaling |
title | Suppressor of cytokine signaling (SOCS)5 ameliorates influenza infection via inhibition of EGFR signaling |
title_full | Suppressor of cytokine signaling (SOCS)5 ameliorates influenza infection via inhibition of EGFR signaling |
title_fullStr | Suppressor of cytokine signaling (SOCS)5 ameliorates influenza infection via inhibition of EGFR signaling |
title_full_unstemmed | Suppressor of cytokine signaling (SOCS)5 ameliorates influenza infection via inhibition of EGFR signaling |
title_short | Suppressor of cytokine signaling (SOCS)5 ameliorates influenza infection via inhibition of EGFR signaling |
title_sort | suppressor of cytokine signaling (socs)5 ameliorates influenza infection via inhibition of egfr signaling |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354519/ https://www.ncbi.nlm.nih.gov/pubmed/28195529 http://dx.doi.org/10.7554/eLife.20444 |
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