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Surfing the clinical trials of mesenchymal stem cell therapy in ischemic cardiomyopathy

While existing remedies failed to fully address the consequences of heart failure, stem cell therapy has been introduced as a promising approach. The present review is a comprehensive appraisal of the impacts of using mesenchymal stem cells (MSCs) in clinical trials mainly conducted on ischemic card...

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Autores principales: Razeghian-Jahromi, Iman, Matta, Anthony G., Canitrot, Ronan, Zibaeenezhad, Mohammad Javad, Razmkhah, Mahboobeh, Safari, Anahid, Nader, Vanessa, Roncalli, Jerome
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220796/
https://www.ncbi.nlm.nih.gov/pubmed/34162424
http://dx.doi.org/10.1186/s13287-021-02443-1
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author Razeghian-Jahromi, Iman
Matta, Anthony G.
Canitrot, Ronan
Zibaeenezhad, Mohammad Javad
Razmkhah, Mahboobeh
Safari, Anahid
Nader, Vanessa
Roncalli, Jerome
author_facet Razeghian-Jahromi, Iman
Matta, Anthony G.
Canitrot, Ronan
Zibaeenezhad, Mohammad Javad
Razmkhah, Mahboobeh
Safari, Anahid
Nader, Vanessa
Roncalli, Jerome
author_sort Razeghian-Jahromi, Iman
collection PubMed
description While existing remedies failed to fully address the consequences of heart failure, stem cell therapy has been introduced as a promising approach. The present review is a comprehensive appraisal of the impacts of using mesenchymal stem cells (MSCs) in clinical trials mainly conducted on ischemic cardiomyopathy. The benefits of MSC therapy for dysfunctional myocardium are likely attributed to numerous secreted paracrine factors and immunomodulatory effects. The positive outcomes associated with MSC therapy are scar size reduction, reverse remodeling, and angiogenesis. Also, a decreasing in the level of chronic inflammatory markers of heart failure progression like TNF-α is observed. The intense inflammatory reaction in the injured myocardial micro-environment predicts a poor response of scar tissue to MSC therapy. Subsequently, the interval delay between myocardial injury and MSC therapy is not yet determined. The optimal requested dose of cells ranges between 100 to 150 million cells. Allogenic MSCs have different advantages compared to autogenic cells and intra-myocardial injection is the preferred delivery route. The safety and efficacy of MSCs-based therapy have been confirmed in numerous studies, however several undefined parameters like route of administration, optimal timing, source of stem cells, and necessary dose are limiting the routine use of MSCs therapeutic approach in clinical practice. Lastly, pre-conditioning of MSCs and using of exosomes mediated MSCs or genetically modified MSCs may improve the overall therapeutic effect. Future prospective studies establishing a constant procedure for MSCs transplantation are required in order to apply MSC therapy in our daily clinical practice and subsequently improving the overall prognosis of ischemic heart failure patients.
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spelling pubmed-82207962021-06-24 Surfing the clinical trials of mesenchymal stem cell therapy in ischemic cardiomyopathy Razeghian-Jahromi, Iman Matta, Anthony G. Canitrot, Ronan Zibaeenezhad, Mohammad Javad Razmkhah, Mahboobeh Safari, Anahid Nader, Vanessa Roncalli, Jerome Stem Cell Res Ther Review While existing remedies failed to fully address the consequences of heart failure, stem cell therapy has been introduced as a promising approach. The present review is a comprehensive appraisal of the impacts of using mesenchymal stem cells (MSCs) in clinical trials mainly conducted on ischemic cardiomyopathy. The benefits of MSC therapy for dysfunctional myocardium are likely attributed to numerous secreted paracrine factors and immunomodulatory effects. The positive outcomes associated with MSC therapy are scar size reduction, reverse remodeling, and angiogenesis. Also, a decreasing in the level of chronic inflammatory markers of heart failure progression like TNF-α is observed. The intense inflammatory reaction in the injured myocardial micro-environment predicts a poor response of scar tissue to MSC therapy. Subsequently, the interval delay between myocardial injury and MSC therapy is not yet determined. The optimal requested dose of cells ranges between 100 to 150 million cells. Allogenic MSCs have different advantages compared to autogenic cells and intra-myocardial injection is the preferred delivery route. The safety and efficacy of MSCs-based therapy have been confirmed in numerous studies, however several undefined parameters like route of administration, optimal timing, source of stem cells, and necessary dose are limiting the routine use of MSCs therapeutic approach in clinical practice. Lastly, pre-conditioning of MSCs and using of exosomes mediated MSCs or genetically modified MSCs may improve the overall therapeutic effect. Future prospective studies establishing a constant procedure for MSCs transplantation are required in order to apply MSC therapy in our daily clinical practice and subsequently improving the overall prognosis of ischemic heart failure patients. BioMed Central 2021-06-23 /pmc/articles/PMC8220796/ /pubmed/34162424 http://dx.doi.org/10.1186/s13287-021-02443-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Razeghian-Jahromi, Iman
Matta, Anthony G.
Canitrot, Ronan
Zibaeenezhad, Mohammad Javad
Razmkhah, Mahboobeh
Safari, Anahid
Nader, Vanessa
Roncalli, Jerome
Surfing the clinical trials of mesenchymal stem cell therapy in ischemic cardiomyopathy
title Surfing the clinical trials of mesenchymal stem cell therapy in ischemic cardiomyopathy
title_full Surfing the clinical trials of mesenchymal stem cell therapy in ischemic cardiomyopathy
title_fullStr Surfing the clinical trials of mesenchymal stem cell therapy in ischemic cardiomyopathy
title_full_unstemmed Surfing the clinical trials of mesenchymal stem cell therapy in ischemic cardiomyopathy
title_short Surfing the clinical trials of mesenchymal stem cell therapy in ischemic cardiomyopathy
title_sort surfing the clinical trials of mesenchymal stem cell therapy in ischemic cardiomyopathy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220796/
https://www.ncbi.nlm.nih.gov/pubmed/34162424
http://dx.doi.org/10.1186/s13287-021-02443-1
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