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The use of mesenchymal stromal cells in the treatment of coronavirus disease 2019
More than seven months into the coronavirus disease -19 (COVID-19) pandemic, infection from the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has led to over 21.2 million cases and resulted in over 760,000 deaths worldwide so far. As a result, COVID-19 has changed all our lives as we...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503434/ https://www.ncbi.nlm.nih.gov/pubmed/32958009 http://dx.doi.org/10.1186/s12967-020-02532-4 |
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author | Canham, Maurice A. Campbell, John D. M. Mountford, Joanne C. |
author_facet | Canham, Maurice A. Campbell, John D. M. Mountford, Joanne C. |
author_sort | Canham, Maurice A. |
collection | PubMed |
description | More than seven months into the coronavirus disease -19 (COVID-19) pandemic, infection from the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has led to over 21.2 million cases and resulted in over 760,000 deaths worldwide so far. As a result, COVID-19 has changed all our lives as we battle to curtail the spread of the infection in the absence of specific therapies against coronaviruses and in anticipation of a proven safe and efficacious vaccine. Common with previous outbreaks of coronavirus infections, SARS and Middle East respiratory syndrome, COVID-19 can lead to acute respiratory distress syndrome (ARDS) that arises due to an imbalanced immune response. While several repurposed antiviral and host-response drugs are under examination as potential treatments, other novel therapeutics are also being explored to alleviate the effects on critically ill patients. The use of mesenchymal stromal cells (MSCs) for COVID-19 has become an attractive avenue down which almost 70 different clinical trial teams have ventured. Successfully trialled for the treatment of other conditions such as multiple sclerosis, osteoarthritis and graft versus host disease, MSCs possess both regenerative and immunomodulatory properties, the latter of which can be harnessed to reduce the severity and longevity of ARDS in patients under intensive care due to SARS-CoV-2 infection. |
format | Online Article Text |
id | pubmed-7503434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75034342020-09-21 The use of mesenchymal stromal cells in the treatment of coronavirus disease 2019 Canham, Maurice A. Campbell, John D. M. Mountford, Joanne C. J Transl Med Review More than seven months into the coronavirus disease -19 (COVID-19) pandemic, infection from the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has led to over 21.2 million cases and resulted in over 760,000 deaths worldwide so far. As a result, COVID-19 has changed all our lives as we battle to curtail the spread of the infection in the absence of specific therapies against coronaviruses and in anticipation of a proven safe and efficacious vaccine. Common with previous outbreaks of coronavirus infections, SARS and Middle East respiratory syndrome, COVID-19 can lead to acute respiratory distress syndrome (ARDS) that arises due to an imbalanced immune response. While several repurposed antiviral and host-response drugs are under examination as potential treatments, other novel therapeutics are also being explored to alleviate the effects on critically ill patients. The use of mesenchymal stromal cells (MSCs) for COVID-19 has become an attractive avenue down which almost 70 different clinical trial teams have ventured. Successfully trialled for the treatment of other conditions such as multiple sclerosis, osteoarthritis and graft versus host disease, MSCs possess both regenerative and immunomodulatory properties, the latter of which can be harnessed to reduce the severity and longevity of ARDS in patients under intensive care due to SARS-CoV-2 infection. BioMed Central 2020-09-21 /pmc/articles/PMC7503434/ /pubmed/32958009 http://dx.doi.org/10.1186/s12967-020-02532-4 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Canham, Maurice A. Campbell, John D. M. Mountford, Joanne C. The use of mesenchymal stromal cells in the treatment of coronavirus disease 2019 |
title | The use of mesenchymal stromal cells in the treatment of coronavirus disease 2019 |
title_full | The use of mesenchymal stromal cells in the treatment of coronavirus disease 2019 |
title_fullStr | The use of mesenchymal stromal cells in the treatment of coronavirus disease 2019 |
title_full_unstemmed | The use of mesenchymal stromal cells in the treatment of coronavirus disease 2019 |
title_short | The use of mesenchymal stromal cells in the treatment of coronavirus disease 2019 |
title_sort | use of mesenchymal stromal cells in the treatment of coronavirus disease 2019 |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503434/ https://www.ncbi.nlm.nih.gov/pubmed/32958009 http://dx.doi.org/10.1186/s12967-020-02532-4 |
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