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Mesenchymal stem cell use in acute respiratory distress syndrome: a potential therapeutic application
Acute respiratory distress syndrome (ARDS) is a condition of acute respiratory failure resulting from noncardiogenic pulmonary edema. It may occur as a consequence of lung infection, sepsis, trauma, aspiration or drug reaction. The pathogenesis of ARDS is understood to be an unregulated inflammatory...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Future Science Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351095/ https://www.ncbi.nlm.nih.gov/pubmed/32670609 http://dx.doi.org/10.2144/fsoa-2020-0048 |
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author | Freitag, Julien Wickham, James Shah, Kiran Tenen, Abi |
author_facet | Freitag, Julien Wickham, James Shah, Kiran Tenen, Abi |
author_sort | Freitag, Julien |
collection | PubMed |
description | Acute respiratory distress syndrome (ARDS) is a condition of acute respiratory failure resulting from noncardiogenic pulmonary edema. It may occur as a consequence of lung infection, sepsis, trauma, aspiration or drug reaction. The pathogenesis of ARDS is understood to be an unregulated inflammatory cascade with both endothelial and epithelial layer damage leading to alveolar fluid collection and pulmonary edema. Despite improved understanding of the cause of ARDS, treatment remains supportive with a mortality rate ranging from 25–40%. Preclinical and early phase clinical trials have highlighted the potential role of mesenchymal stem cells in combating the inflammatory cascade through immunomodulatory mechanisms and assisting in tissue repair. |
format | Online Article Text |
id | pubmed-7351095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Future Science Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-73510952020-07-14 Mesenchymal stem cell use in acute respiratory distress syndrome: a potential therapeutic application Freitag, Julien Wickham, James Shah, Kiran Tenen, Abi Future Sci OA Review Acute respiratory distress syndrome (ARDS) is a condition of acute respiratory failure resulting from noncardiogenic pulmonary edema. It may occur as a consequence of lung infection, sepsis, trauma, aspiration or drug reaction. The pathogenesis of ARDS is understood to be an unregulated inflammatory cascade with both endothelial and epithelial layer damage leading to alveolar fluid collection and pulmonary edema. Despite improved understanding of the cause of ARDS, treatment remains supportive with a mortality rate ranging from 25–40%. Preclinical and early phase clinical trials have highlighted the potential role of mesenchymal stem cells in combating the inflammatory cascade through immunomodulatory mechanisms and assisting in tissue repair. Future Science Ltd 2020-05-12 /pmc/articles/PMC7351095/ /pubmed/32670609 http://dx.doi.org/10.2144/fsoa-2020-0048 Text en © 2020 Julien Freitag This work is licensed under the Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Review Freitag, Julien Wickham, James Shah, Kiran Tenen, Abi Mesenchymal stem cell use in acute respiratory distress syndrome: a potential therapeutic application |
title | Mesenchymal stem cell use in acute respiratory distress syndrome: a potential therapeutic application |
title_full | Mesenchymal stem cell use in acute respiratory distress syndrome: a potential therapeutic application |
title_fullStr | Mesenchymal stem cell use in acute respiratory distress syndrome: a potential therapeutic application |
title_full_unstemmed | Mesenchymal stem cell use in acute respiratory distress syndrome: a potential therapeutic application |
title_short | Mesenchymal stem cell use in acute respiratory distress syndrome: a potential therapeutic application |
title_sort | mesenchymal stem cell use in acute respiratory distress syndrome: a potential therapeutic application |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351095/ https://www.ncbi.nlm.nih.gov/pubmed/32670609 http://dx.doi.org/10.2144/fsoa-2020-0048 |
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