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Mesenchymal stem cell therapy for acute respiratory distress syndrome: from basic to clinics
The 2019 novel coronavirus disease (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has occurred in China and around the world. SARS-CoV-2-infected patients with severe pneumonia rapidly develop acute respiratory distress syndrome (ARDS) and die of multiple org...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Higher Education Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282699/ https://www.ncbi.nlm.nih.gov/pubmed/32519302 http://dx.doi.org/10.1007/s13238-020-00738-2 |
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author | Qin, Hua Zhao, Andong |
author_facet | Qin, Hua Zhao, Andong |
author_sort | Qin, Hua |
collection | PubMed |
description | The 2019 novel coronavirus disease (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has occurred in China and around the world. SARS-CoV-2-infected patients with severe pneumonia rapidly develop acute respiratory distress syndrome (ARDS) and die of multiple organ failure. Despite advances in supportive care approaches, ARDS is still associated with high mortality and morbidity. Mesenchymal stem cell (MSC)-based therapy may be an potential alternative strategy for treating ARDS by targeting the various pathophysiological events of ARDS. By releasing a variety of paracrine factors and extracellular vesicles, MSC can exert anti-inflammatory, anti-apoptotic, anti-microbial, and pro-angiogenic effects, promote bacterial and alveolar fluid clearance, disrupt the pulmonary endothelial and epithelial cell damage, eventually avoiding the lung and distal organ injuries to rescue patients with ARDS. An increasing number of experimental animal studies and early clinical studies verify the safety and efficacy of MSC therapy in ARDS. Since low cell engraftment and survival in lung limit MSC therapeutic potentials, several strategies have been developed to enhance their engraftment in the lung and their intrinsic, therapeutic properties. Here, we provide a comprehensive review of the mechanisms and optimization of MSC therapy in ARDS and highlighted the potentials and possible barriers of MSC therapy for COVID-19 patients with ARDS. |
format | Online Article Text |
id | pubmed-7282699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Higher Education Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-72826992020-06-10 Mesenchymal stem cell therapy for acute respiratory distress syndrome: from basic to clinics Qin, Hua Zhao, Andong Protein Cell Review The 2019 novel coronavirus disease (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has occurred in China and around the world. SARS-CoV-2-infected patients with severe pneumonia rapidly develop acute respiratory distress syndrome (ARDS) and die of multiple organ failure. Despite advances in supportive care approaches, ARDS is still associated with high mortality and morbidity. Mesenchymal stem cell (MSC)-based therapy may be an potential alternative strategy for treating ARDS by targeting the various pathophysiological events of ARDS. By releasing a variety of paracrine factors and extracellular vesicles, MSC can exert anti-inflammatory, anti-apoptotic, anti-microbial, and pro-angiogenic effects, promote bacterial and alveolar fluid clearance, disrupt the pulmonary endothelial and epithelial cell damage, eventually avoiding the lung and distal organ injuries to rescue patients with ARDS. An increasing number of experimental animal studies and early clinical studies verify the safety and efficacy of MSC therapy in ARDS. Since low cell engraftment and survival in lung limit MSC therapeutic potentials, several strategies have been developed to enhance their engraftment in the lung and their intrinsic, therapeutic properties. Here, we provide a comprehensive review of the mechanisms and optimization of MSC therapy in ARDS and highlighted the potentials and possible barriers of MSC therapy for COVID-19 patients with ARDS. Higher Education Press 2020-06-09 2020-10 /pmc/articles/PMC7282699/ /pubmed/32519302 http://dx.doi.org/10.1007/s13238-020-00738-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Review Qin, Hua Zhao, Andong Mesenchymal stem cell therapy for acute respiratory distress syndrome: from basic to clinics |
title | Mesenchymal stem cell therapy for acute respiratory distress syndrome: from basic to clinics |
title_full | Mesenchymal stem cell therapy for acute respiratory distress syndrome: from basic to clinics |
title_fullStr | Mesenchymal stem cell therapy for acute respiratory distress syndrome: from basic to clinics |
title_full_unstemmed | Mesenchymal stem cell therapy for acute respiratory distress syndrome: from basic to clinics |
title_short | Mesenchymal stem cell therapy for acute respiratory distress syndrome: from basic to clinics |
title_sort | mesenchymal stem cell therapy for acute respiratory distress syndrome: from basic to clinics |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282699/ https://www.ncbi.nlm.nih.gov/pubmed/32519302 http://dx.doi.org/10.1007/s13238-020-00738-2 |
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