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Immunotherapy of multisystem inflammatory syndrome in children (MIS-C) following COVID-19 through mesenchymal stem cells

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a new type of coronavirus causing coronavirus 2019 (COVID-19) that was first observed in Wuhan, China, in Dec. 2019. An inflammatory immune response targeting children appeared during the pandemic, which was associated with COVID-19 nam...

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Autores principales: Suksatan, Wanich, Chupradit, Supat, Yumashev, Alexei Valerievich, Ravali, Sahithya, Shalaby, Mohammed Nader, Mustafa, Yasser Fakri, Kurochkin, Anatoley, Siahmansouri, Homayoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487784/
https://www.ncbi.nlm.nih.gov/pubmed/34627083
http://dx.doi.org/10.1016/j.intimp.2021.108217
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author Suksatan, Wanich
Chupradit, Supat
Yumashev, Alexei Valerievich
Ravali, Sahithya
Shalaby, Mohammed Nader
Mustafa, Yasser Fakri
Kurochkin, Anatoley
Siahmansouri, Homayoon
author_facet Suksatan, Wanich
Chupradit, Supat
Yumashev, Alexei Valerievich
Ravali, Sahithya
Shalaby, Mohammed Nader
Mustafa, Yasser Fakri
Kurochkin, Anatoley
Siahmansouri, Homayoon
author_sort Suksatan, Wanich
collection PubMed
description Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a new type of coronavirus causing coronavirus 2019 (COVID-19) that was first observed in Wuhan, China, in Dec. 2019. An inflammatory immune response targeting children appeared during the pandemic, which was associated with COVID-19 named multisystem inflammatory syndrome in children (MIS-C). Characteristics of MIS-C include the classic inflammation findings, multi-organ dysfunction, and fever as the cardinal feature. Up to now, no specific therapy has been identified for MIS-C. Currently, considerable progress has been obtained in the MIS-C treatment by cell therapy, specially Mesenchymal stem cells (MSCs). Unique properties have been reported for MSCs, such as various resources for purification of cell, high proliferation, self-renewal, non-invasive procedure, tissue regenerator, multidirectional differentiation, and immunosuppression. As indicated by a recent clinical research, MSCs have the ability of reducing disease inflammation and severity in children with MIS-C. In the present review study, the benefits and characteristics of MSCs and exosomes are discussed for treating patients with MIS-C.
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spelling pubmed-84877842021-10-04 Immunotherapy of multisystem inflammatory syndrome in children (MIS-C) following COVID-19 through mesenchymal stem cells Suksatan, Wanich Chupradit, Supat Yumashev, Alexei Valerievich Ravali, Sahithya Shalaby, Mohammed Nader Mustafa, Yasser Fakri Kurochkin, Anatoley Siahmansouri, Homayoon Int Immunopharmacol Article Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a new type of coronavirus causing coronavirus 2019 (COVID-19) that was first observed in Wuhan, China, in Dec. 2019. An inflammatory immune response targeting children appeared during the pandemic, which was associated with COVID-19 named multisystem inflammatory syndrome in children (MIS-C). Characteristics of MIS-C include the classic inflammation findings, multi-organ dysfunction, and fever as the cardinal feature. Up to now, no specific therapy has been identified for MIS-C. Currently, considerable progress has been obtained in the MIS-C treatment by cell therapy, specially Mesenchymal stem cells (MSCs). Unique properties have been reported for MSCs, such as various resources for purification of cell, high proliferation, self-renewal, non-invasive procedure, tissue regenerator, multidirectional differentiation, and immunosuppression. As indicated by a recent clinical research, MSCs have the ability of reducing disease inflammation and severity in children with MIS-C. In the present review study, the benefits and characteristics of MSCs and exosomes are discussed for treating patients with MIS-C. Elsevier B.V. 2021-12 2021-10-04 /pmc/articles/PMC8487784/ /pubmed/34627083 http://dx.doi.org/10.1016/j.intimp.2021.108217 Text en © 2021 Elsevier B.V. All rights reserved. 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
Suksatan, Wanich
Chupradit, Supat
Yumashev, Alexei Valerievich
Ravali, Sahithya
Shalaby, Mohammed Nader
Mustafa, Yasser Fakri
Kurochkin, Anatoley
Siahmansouri, Homayoon
Immunotherapy of multisystem inflammatory syndrome in children (MIS-C) following COVID-19 through mesenchymal stem cells
title Immunotherapy of multisystem inflammatory syndrome in children (MIS-C) following COVID-19 through mesenchymal stem cells
title_full Immunotherapy of multisystem inflammatory syndrome in children (MIS-C) following COVID-19 through mesenchymal stem cells
title_fullStr Immunotherapy of multisystem inflammatory syndrome in children (MIS-C) following COVID-19 through mesenchymal stem cells
title_full_unstemmed Immunotherapy of multisystem inflammatory syndrome in children (MIS-C) following COVID-19 through mesenchymal stem cells
title_short Immunotherapy of multisystem inflammatory syndrome in children (MIS-C) following COVID-19 through mesenchymal stem cells
title_sort immunotherapy of multisystem inflammatory syndrome in children (mis-c) following covid-19 through mesenchymal stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487784/
https://www.ncbi.nlm.nih.gov/pubmed/34627083
http://dx.doi.org/10.1016/j.intimp.2021.108217
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