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The role of mesenchymal stromal cells in immune modulation of COVID-19: focus on cytokine storm

The outbreak of coronavirus disease 2019 (COVID-19) pandemic is quickly spreading all over the world. This virus, which is called SARS-CoV-2, has infected tens of thousands of people. Based on symptoms, the pathogenesis of acute respiratory illness is responsible for highly homogenous coronaviruses...

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Autores principales: Kavianpour, Maria, Saleh, Mahshid, Verdi, Javad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499002/
https://www.ncbi.nlm.nih.gov/pubmed/32948252
http://dx.doi.org/10.1186/s13287-020-01849-7
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author Kavianpour, Maria
Saleh, Mahshid
Verdi, Javad
author_facet Kavianpour, Maria
Saleh, Mahshid
Verdi, Javad
author_sort Kavianpour, Maria
collection PubMed
description The outbreak of coronavirus disease 2019 (COVID-19) pandemic is quickly spreading all over the world. This virus, which is called SARS-CoV-2, has infected tens of thousands of people. Based on symptoms, the pathogenesis of acute respiratory illness is responsible for highly homogenous coronaviruses as well as other pathogens. Evidence suggests that high inflammation rates, oxidation, and overwhelming immune response probably contribute to pathology of COVID-19. COVID-19 causes cytokine storm, which subsequently leads to acute respiratory distress syndrome (ARDS), often ending up in the death of patients. Mesenchymal stem cells (MSCs) are multipotential stem cells that are recognized via self-renewal capacity, generation of clonal populations, and multilineage differentiation. MSCs are present in nearly all tissues of the body, playing an essential role in repair and generation of tissues. Furthermore, MSCs have broad immunoregulatory properties through the interaction of immune cells in both innate and adaptive immune systems, leading to immunosuppression of many effector activities. MSCs can reduce the cytokine storm produced by coronavirus infection. In a number of studies, the administration of these cells has been beneficial for COVID-19 patients. Also, MSCs may be able to improve pulmonary fibrosis and lung function. In this review, we will review the newest research findings regarding MSC-based immunomodulation in patients with COVID-19.
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spelling pubmed-74990022020-09-18 The role of mesenchymal stromal cells in immune modulation of COVID-19: focus on cytokine storm Kavianpour, Maria Saleh, Mahshid Verdi, Javad Stem Cell Res Ther Review The outbreak of coronavirus disease 2019 (COVID-19) pandemic is quickly spreading all over the world. This virus, which is called SARS-CoV-2, has infected tens of thousands of people. Based on symptoms, the pathogenesis of acute respiratory illness is responsible for highly homogenous coronaviruses as well as other pathogens. Evidence suggests that high inflammation rates, oxidation, and overwhelming immune response probably contribute to pathology of COVID-19. COVID-19 causes cytokine storm, which subsequently leads to acute respiratory distress syndrome (ARDS), often ending up in the death of patients. Mesenchymal stem cells (MSCs) are multipotential stem cells that are recognized via self-renewal capacity, generation of clonal populations, and multilineage differentiation. MSCs are present in nearly all tissues of the body, playing an essential role in repair and generation of tissues. Furthermore, MSCs have broad immunoregulatory properties through the interaction of immune cells in both innate and adaptive immune systems, leading to immunosuppression of many effector activities. MSCs can reduce the cytokine storm produced by coronavirus infection. In a number of studies, the administration of these cells has been beneficial for COVID-19 patients. Also, MSCs may be able to improve pulmonary fibrosis and lung function. In this review, we will review the newest research findings regarding MSC-based immunomodulation in patients with COVID-19. BioMed Central 2020-09-18 /pmc/articles/PMC7499002/ /pubmed/32948252 http://dx.doi.org/10.1186/s13287-020-01849-7 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
Kavianpour, Maria
Saleh, Mahshid
Verdi, Javad
The role of mesenchymal stromal cells in immune modulation of COVID-19: focus on cytokine storm
title The role of mesenchymal stromal cells in immune modulation of COVID-19: focus on cytokine storm
title_full The role of mesenchymal stromal cells in immune modulation of COVID-19: focus on cytokine storm
title_fullStr The role of mesenchymal stromal cells in immune modulation of COVID-19: focus on cytokine storm
title_full_unstemmed The role of mesenchymal stromal cells in immune modulation of COVID-19: focus on cytokine storm
title_short The role of mesenchymal stromal cells in immune modulation of COVID-19: focus on cytokine storm
title_sort role of mesenchymal stromal cells in immune modulation of covid-19: focus on cytokine storm
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499002/
https://www.ncbi.nlm.nih.gov/pubmed/32948252
http://dx.doi.org/10.1186/s13287-020-01849-7
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