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

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作者
Iman Razeghian-Jahromi
Anthony G. Matta
Ronan Canitrot
Mohammad Javad Zibaeenezhad
Mahboobeh Razmkhah
Anahid Safari
Vanessa Nader
Jerome Roncalli
机构
[1] Shiraz University of Medical Sciences,Cardiovascular Research Center
[2] University Hospital of Toulouse,Department of Cardiology, Institute CARDIOMET
[3] Holy Spirit University of Kaslik,Faculty of medicine
[4] Shiraz University of Medical Sciences,Shiraz Institute for Cancer Research, School of Medicine
[5] Shiraz University of Medical Sciences,Stem Cells Technology Research Center
[6] Lebanese University,Faculty of Pharmacy
[7] Service de Cardiologie A,undefined
[8] CHU de Toulouse,undefined
[9] Hôpital de Rangueil,undefined
关键词
Mesenchymal stem cells; Ischemic cardiomyopathy; Clinical trials;
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摘要
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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