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Elucidating novel disease mechanisms in severe asthma
Corticosteroids are broadly active and potent anti-inflammatory agents that, despite the introduction of biologics, remain as the mainstay therapy for many chronic inflammatory diseases, including inflammatory bowel diseases, nephrotic syndrome, rheumatoid arthritis, chronic obstructive pulmonary di...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973321/ https://www.ncbi.nlm.nih.gov/pubmed/27525064 http://dx.doi.org/10.1038/cti.2016.37 |
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author | Kim, Richard Y Rae, Brittany Neal, Rachel Donovan, Chantal Pinkerton, James Balachandran, Lohis Starkey, Malcolm R Knight, Darryl A Horvat, Jay C Hansbro, Philip M |
author_facet | Kim, Richard Y Rae, Brittany Neal, Rachel Donovan, Chantal Pinkerton, James Balachandran, Lohis Starkey, Malcolm R Knight, Darryl A Horvat, Jay C Hansbro, Philip M |
author_sort | Kim, Richard Y |
collection | PubMed |
description | Corticosteroids are broadly active and potent anti-inflammatory agents that, despite the introduction of biologics, remain as the mainstay therapy for many chronic inflammatory diseases, including inflammatory bowel diseases, nephrotic syndrome, rheumatoid arthritis, chronic obstructive pulmonary disease and asthma. Significantly, there are cohorts of these patients with poor sensitivity to steroid treatment even with high doses, which can lead to many iatrogenic side effects. The dose-limiting toxicity of corticosteroids, and the lack of effective therapeutic alternatives, leads to substantial excess morbidity and healthcare expenditure. We have developed novel murine models of respiratory infection-induced, severe, steroid-resistant asthma that recapitulate the hallmark features of the human disease. These models can be used to elucidate novel disease mechanisms and identify new therapeutic targets in severe asthma. Hypothesis-driven studies can elucidate the roles of specific factors and pathways. Alternatively, 'Omics approaches can be used to rapidly generate new targets. Similar approaches can be used in other diseases. |
format | Online Article Text |
id | pubmed-4973321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49733212016-08-12 Elucidating novel disease mechanisms in severe asthma Kim, Richard Y Rae, Brittany Neal, Rachel Donovan, Chantal Pinkerton, James Balachandran, Lohis Starkey, Malcolm R Knight, Darryl A Horvat, Jay C Hansbro, Philip M Clin Transl Immunology Review Corticosteroids are broadly active and potent anti-inflammatory agents that, despite the introduction of biologics, remain as the mainstay therapy for many chronic inflammatory diseases, including inflammatory bowel diseases, nephrotic syndrome, rheumatoid arthritis, chronic obstructive pulmonary disease and asthma. Significantly, there are cohorts of these patients with poor sensitivity to steroid treatment even with high doses, which can lead to many iatrogenic side effects. The dose-limiting toxicity of corticosteroids, and the lack of effective therapeutic alternatives, leads to substantial excess morbidity and healthcare expenditure. We have developed novel murine models of respiratory infection-induced, severe, steroid-resistant asthma that recapitulate the hallmark features of the human disease. These models can be used to elucidate novel disease mechanisms and identify new therapeutic targets in severe asthma. Hypothesis-driven studies can elucidate the roles of specific factors and pathways. Alternatively, 'Omics approaches can be used to rapidly generate new targets. Similar approaches can be used in other diseases. Nature Publishing Group 2016-07-15 /pmc/articles/PMC4973321/ /pubmed/27525064 http://dx.doi.org/10.1038/cti.2016.37 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Review Kim, Richard Y Rae, Brittany Neal, Rachel Donovan, Chantal Pinkerton, James Balachandran, Lohis Starkey, Malcolm R Knight, Darryl A Horvat, Jay C Hansbro, Philip M Elucidating novel disease mechanisms in severe asthma |
title | Elucidating novel disease mechanisms in severe asthma |
title_full | Elucidating novel disease mechanisms in severe asthma |
title_fullStr | Elucidating novel disease mechanisms in severe asthma |
title_full_unstemmed | Elucidating novel disease mechanisms in severe asthma |
title_short | Elucidating novel disease mechanisms in severe asthma |
title_sort | elucidating novel disease mechanisms in severe asthma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973321/ https://www.ncbi.nlm.nih.gov/pubmed/27525064 http://dx.doi.org/10.1038/cti.2016.37 |
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