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SARS-CoV-2 infection and stem cells: Interaction and intervention

The emergence of the novel severe acute respiratory coronavirus 2 (SARS-CoV-2) in China and its rapid national and international spread have created a global health emergency. The resemblance with SARS-CoV in spike protein suggests that SARS-CoV-2 employs spike–driven entry into angiotensin-converti...

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Autores principales: Yu, Fenggang, Jia, Rufu, Tang, Yongyong, Liu, Jin, Wei, Benjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier B.V. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7263221/
https://www.ncbi.nlm.nih.gov/pubmed/32570174
http://dx.doi.org/10.1016/j.scr.2020.101859
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author Yu, Fenggang
Jia, Rufu
Tang, Yongyong
Liu, Jin
Wei, Benjie
author_facet Yu, Fenggang
Jia, Rufu
Tang, Yongyong
Liu, Jin
Wei, Benjie
author_sort Yu, Fenggang
collection PubMed
description The emergence of the novel severe acute respiratory coronavirus 2 (SARS-CoV-2) in China and its rapid national and international spread have created a global health emergency. The resemblance with SARS-CoV in spike protein suggests that SARS-CoV-2 employs spike–driven entry into angiotensin-converting enzyme 2 (ACE2)-expressing cells. From a stem cell perspective, this review focuses on the possible involvement of ACE2(+) stem/progenitor cells from both the upper and lower respiratory tracts in coronavirus infection. Viral infection-associated acute respiratory distress syndrome and acute lung injury occur because of dysregulation of the immune response. Mesenchymal stem cells appear to be a promising cell therapy given that they favorably modulate the immune response to reduce lung injury. The use of exogenous stem cells may lead to lung repair. Therefore, intervention by transplantation of exogenous stem cells may be required to replace, repair, remodel, and regenerate lung tissue in survivors infected with coronavirus. Ultimately, vaccines, natural killer cells and induced-pluripotent stem cell-derived virus-specific cytotoxic T lymphocytes may offer off-the-shelf therapeutics for preventing coronavirus reemergence.
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spelling pubmed-72632212020-06-02 SARS-CoV-2 infection and stem cells: Interaction and intervention Yu, Fenggang Jia, Rufu Tang, Yongyong Liu, Jin Wei, Benjie Stem Cell Res Article The emergence of the novel severe acute respiratory coronavirus 2 (SARS-CoV-2) in China and its rapid national and international spread have created a global health emergency. The resemblance with SARS-CoV in spike protein suggests that SARS-CoV-2 employs spike–driven entry into angiotensin-converting enzyme 2 (ACE2)-expressing cells. From a stem cell perspective, this review focuses on the possible involvement of ACE2(+) stem/progenitor cells from both the upper and lower respiratory tracts in coronavirus infection. Viral infection-associated acute respiratory distress syndrome and acute lung injury occur because of dysregulation of the immune response. Mesenchymal stem cells appear to be a promising cell therapy given that they favorably modulate the immune response to reduce lung injury. The use of exogenous stem cells may lead to lung repair. Therefore, intervention by transplantation of exogenous stem cells may be required to replace, repair, remodel, and regenerate lung tissue in survivors infected with coronavirus. Ultimately, vaccines, natural killer cells and induced-pluripotent stem cell-derived virus-specific cytotoxic T lymphocytes may offer off-the-shelf therapeutics for preventing coronavirus reemergence. Published by Elsevier B.V. 2020-07 2020-06-01 /pmc/articles/PMC7263221/ /pubmed/32570174 http://dx.doi.org/10.1016/j.scr.2020.101859 Text en © 2020 Published by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Yu, Fenggang
Jia, Rufu
Tang, Yongyong
Liu, Jin
Wei, Benjie
SARS-CoV-2 infection and stem cells: Interaction and intervention
title SARS-CoV-2 infection and stem cells: Interaction and intervention
title_full SARS-CoV-2 infection and stem cells: Interaction and intervention
title_fullStr SARS-CoV-2 infection and stem cells: Interaction and intervention
title_full_unstemmed SARS-CoV-2 infection and stem cells: Interaction and intervention
title_short SARS-CoV-2 infection and stem cells: Interaction and intervention
title_sort sars-cov-2 infection and stem cells: interaction and intervention
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7263221/
https://www.ncbi.nlm.nih.gov/pubmed/32570174
http://dx.doi.org/10.1016/j.scr.2020.101859
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