Cargando…

Exploring the Immunomodulatory Aspect of Mesenchymal Stem Cells for Treatment of Severe Coronavirus Disease 19

Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is an enveloped, positive sense, single stranded RNA (+ssRNA) virus, belonging to the genus Betacoronavirus and family Coronaviridae. It is primarily transmitted from infected persons to healthy ones through inhalation of virus-laden respi...

Descripción completa

Detalles Bibliográficos
Autores principales: Chaudhary, Jitendra Kumar, Saini, Deepika, Chaudhary, Pankaj Kumar, Maurya, Anurag, Verma, Ganesh Kumar, Gupta, Akhilesh Kumar, Roshan, Rakesh, Vats, Tarun Kumar, Garg, Nidhi, Yadav, Deepika, Kant, Nimita, Meena, Anil Kumar, Mirza-Shariff, Anissa Atif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322532/
https://www.ncbi.nlm.nih.gov/pubmed/35883618
http://dx.doi.org/10.3390/cells11142175
_version_ 1784756328053342208
author Chaudhary, Jitendra Kumar
Saini, Deepika
Chaudhary, Pankaj Kumar
Maurya, Anurag
Verma, Ganesh Kumar
Gupta, Akhilesh Kumar
Roshan, Rakesh
Vats, Tarun Kumar
Garg, Nidhi
Yadav, Deepika
Kant, Nimita
Meena, Anil Kumar
Mirza-Shariff, Anissa Atif
author_facet Chaudhary, Jitendra Kumar
Saini, Deepika
Chaudhary, Pankaj Kumar
Maurya, Anurag
Verma, Ganesh Kumar
Gupta, Akhilesh Kumar
Roshan, Rakesh
Vats, Tarun Kumar
Garg, Nidhi
Yadav, Deepika
Kant, Nimita
Meena, Anil Kumar
Mirza-Shariff, Anissa Atif
author_sort Chaudhary, Jitendra Kumar
collection PubMed
description Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is an enveloped, positive sense, single stranded RNA (+ssRNA) virus, belonging to the genus Betacoronavirus and family Coronaviridae. It is primarily transmitted from infected persons to healthy ones through inhalation of virus-laden respiratory droplets. After an average incubation period of 2–14 days, the majority of infected individuals remain asymptomatic and/or mildly symptomatic, whereas the remaining individuals manifest a myriad of clinical symptoms, including fever, sore throat, dry cough, fatigue, chest pain, and breathlessness. SARS-CoV-2 exploits the angiotensin converting enzyme 2 (ACE-2) receptor for cellular invasion, and lungs are amongst the most adversely affected organs in the body. Thereupon, immune responses are elicited, which may devolve into a cytokine storm characterized by enhanced secretion of multitude of inflammatory cytokines/chemokines and growth factors, such as interleukin (IL)-2, IL-6, IL-7, IL-8, IL-9, tumor necrosis factor alpha (TNF-α), granulocyte colony-stimulating factor (GCSF), basic fibroblast growth factor 2 (bFGF2), monocyte chemotactic protein-1 (MCP1), interferon-inducible protein 10 (IP10), macrophage inflammatory protein 1A (MIP1A), platelet-derived growth factor subunit B (PDGFB), and vascular endothelial factor (VEGF)-A. The systemic persistence of inflammatory molecules causes widespread histological injury, leading to functional deterioration of the infected organ(s). Although multiple treatment modalities with varying effectiveness are being employed, nevertheless, there is no curative COVID-19 therapy available to date. In this regard, one plausible supportive therapeutic modality may involve administration of mesenchymal stem cells (MSCs) and/or MSC-derived bioactive factors-based secretome to critically ill COVID-19 patients with the intention of accomplishing better clinical outcome owing to their empirically established beneficial effects. MSCs are well established adult stem cells (ASCs) with respect to their immunomodulatory, anti-inflammatory, anti-oxidative, anti-apoptotic, pro-angiogenic, and pro-regenerative properties. The immunomodulatory capabilities of MSCs are not constitutive but rather are highly dependent on a holistic niche. Following intravenous infusion, MSCs are known to undergo considerable histological trapping in the lungs and, therefore, become well positioned to directly engage with lung infiltrating immune cells, and thereby mitigate excessive inflammation and reverse/regenerate damaged alveolar epithelial cells and associated tissue post SARS-CoV-2 infection. Considering the myriad of abovementioned biologically beneficial properties and emerging translational insights, MSCs may be used as potential supportive therapy to counteract cytokine storms and reduce disease severity, thereby facilitating speedy recovery and health restoration.
format Online
Article
Text
id pubmed-9322532
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-93225322022-07-27 Exploring the Immunomodulatory Aspect of Mesenchymal Stem Cells for Treatment of Severe Coronavirus Disease 19 Chaudhary, Jitendra Kumar Saini, Deepika Chaudhary, Pankaj Kumar Maurya, Anurag Verma, Ganesh Kumar Gupta, Akhilesh Kumar Roshan, Rakesh Vats, Tarun Kumar Garg, Nidhi Yadav, Deepika Kant, Nimita Meena, Anil Kumar Mirza-Shariff, Anissa Atif Cells Review Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is an enveloped, positive sense, single stranded RNA (+ssRNA) virus, belonging to the genus Betacoronavirus and family Coronaviridae. It is primarily transmitted from infected persons to healthy ones through inhalation of virus-laden respiratory droplets. After an average incubation period of 2–14 days, the majority of infected individuals remain asymptomatic and/or mildly symptomatic, whereas the remaining individuals manifest a myriad of clinical symptoms, including fever, sore throat, dry cough, fatigue, chest pain, and breathlessness. SARS-CoV-2 exploits the angiotensin converting enzyme 2 (ACE-2) receptor for cellular invasion, and lungs are amongst the most adversely affected organs in the body. Thereupon, immune responses are elicited, which may devolve into a cytokine storm characterized by enhanced secretion of multitude of inflammatory cytokines/chemokines and growth factors, such as interleukin (IL)-2, IL-6, IL-7, IL-8, IL-9, tumor necrosis factor alpha (TNF-α), granulocyte colony-stimulating factor (GCSF), basic fibroblast growth factor 2 (bFGF2), monocyte chemotactic protein-1 (MCP1), interferon-inducible protein 10 (IP10), macrophage inflammatory protein 1A (MIP1A), platelet-derived growth factor subunit B (PDGFB), and vascular endothelial factor (VEGF)-A. The systemic persistence of inflammatory molecules causes widespread histological injury, leading to functional deterioration of the infected organ(s). Although multiple treatment modalities with varying effectiveness are being employed, nevertheless, there is no curative COVID-19 therapy available to date. In this regard, one plausible supportive therapeutic modality may involve administration of mesenchymal stem cells (MSCs) and/or MSC-derived bioactive factors-based secretome to critically ill COVID-19 patients with the intention of accomplishing better clinical outcome owing to their empirically established beneficial effects. MSCs are well established adult stem cells (ASCs) with respect to their immunomodulatory, anti-inflammatory, anti-oxidative, anti-apoptotic, pro-angiogenic, and pro-regenerative properties. The immunomodulatory capabilities of MSCs are not constitutive but rather are highly dependent on a holistic niche. Following intravenous infusion, MSCs are known to undergo considerable histological trapping in the lungs and, therefore, become well positioned to directly engage with lung infiltrating immune cells, and thereby mitigate excessive inflammation and reverse/regenerate damaged alveolar epithelial cells and associated tissue post SARS-CoV-2 infection. Considering the myriad of abovementioned biologically beneficial properties and emerging translational insights, MSCs may be used as potential supportive therapy to counteract cytokine storms and reduce disease severity, thereby facilitating speedy recovery and health restoration. MDPI 2022-07-12 /pmc/articles/PMC9322532/ /pubmed/35883618 http://dx.doi.org/10.3390/cells11142175 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Chaudhary, Jitendra Kumar
Saini, Deepika
Chaudhary, Pankaj Kumar
Maurya, Anurag
Verma, Ganesh Kumar
Gupta, Akhilesh Kumar
Roshan, Rakesh
Vats, Tarun Kumar
Garg, Nidhi
Yadav, Deepika
Kant, Nimita
Meena, Anil Kumar
Mirza-Shariff, Anissa Atif
Exploring the Immunomodulatory Aspect of Mesenchymal Stem Cells for Treatment of Severe Coronavirus Disease 19
title Exploring the Immunomodulatory Aspect of Mesenchymal Stem Cells for Treatment of Severe Coronavirus Disease 19
title_full Exploring the Immunomodulatory Aspect of Mesenchymal Stem Cells for Treatment of Severe Coronavirus Disease 19
title_fullStr Exploring the Immunomodulatory Aspect of Mesenchymal Stem Cells for Treatment of Severe Coronavirus Disease 19
title_full_unstemmed Exploring the Immunomodulatory Aspect of Mesenchymal Stem Cells for Treatment of Severe Coronavirus Disease 19
title_short Exploring the Immunomodulatory Aspect of Mesenchymal Stem Cells for Treatment of Severe Coronavirus Disease 19
title_sort exploring the immunomodulatory aspect of mesenchymal stem cells for treatment of severe coronavirus disease 19
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322532/
https://www.ncbi.nlm.nih.gov/pubmed/35883618
http://dx.doi.org/10.3390/cells11142175
work_keys_str_mv AT chaudharyjitendrakumar exploringtheimmunomodulatoryaspectofmesenchymalstemcellsfortreatmentofseverecoronavirusdisease19
AT sainideepika exploringtheimmunomodulatoryaspectofmesenchymalstemcellsfortreatmentofseverecoronavirusdisease19
AT chaudharypankajkumar exploringtheimmunomodulatoryaspectofmesenchymalstemcellsfortreatmentofseverecoronavirusdisease19
AT mauryaanurag exploringtheimmunomodulatoryaspectofmesenchymalstemcellsfortreatmentofseverecoronavirusdisease19
AT vermaganeshkumar exploringtheimmunomodulatoryaspectofmesenchymalstemcellsfortreatmentofseverecoronavirusdisease19
AT guptaakhileshkumar exploringtheimmunomodulatoryaspectofmesenchymalstemcellsfortreatmentofseverecoronavirusdisease19
AT roshanrakesh exploringtheimmunomodulatoryaspectofmesenchymalstemcellsfortreatmentofseverecoronavirusdisease19
AT vatstarunkumar exploringtheimmunomodulatoryaspectofmesenchymalstemcellsfortreatmentofseverecoronavirusdisease19
AT gargnidhi exploringtheimmunomodulatoryaspectofmesenchymalstemcellsfortreatmentofseverecoronavirusdisease19
AT yadavdeepika exploringtheimmunomodulatoryaspectofmesenchymalstemcellsfortreatmentofseverecoronavirusdisease19
AT kantnimita exploringtheimmunomodulatoryaspectofmesenchymalstemcellsfortreatmentofseverecoronavirusdisease19
AT meenaanilkumar exploringtheimmunomodulatoryaspectofmesenchymalstemcellsfortreatmentofseverecoronavirusdisease19
AT mirzashariffanissaatif exploringtheimmunomodulatoryaspectofmesenchymalstemcellsfortreatmentofseverecoronavirusdisease19