Cellular Therapy for Heart Failure
Peter J Psaltis1, Nisha Schwarz, Deborah Toledo-Flores
1Co-Director of Vascular Research Centre, Heart Health Theme, South Australian Health and Medical Research Institute, North Terrace, Adelaide, South Australia, Australia 5000. peter.psaltis@sahmri.com.
Insights
Cellular transplantation shows promise for heart failure (HF) by facilitating cardiac repair through stem cell paracrine effects. Further research is needed to overcome challenges and optimize cell therapy for managing HF.
Area of Science:
- Cardiology
- Regenerative Medicine
- Stem Cell Biology
Background:
- Heart failure (HF) pathogenesis involves complex myocardial changes, with conventional treatments inadequately addressing cardiomyocyte loss.
- Cellular transplantation has evolved over two decades to address HF, utilizing various cell types and delivery routes.
Purpose of the Study:
- To review preclinical and clinical evidence of stem cell therapy for cardiomyopathy and HF.
- To outline lessons learned and identify challenges for realizing cell therapy's full potential in HF management.
Main Methods:
- Review of preclinical models and early-phase human studies on cell transplantation for HF.
- Analysis of stem cell types, delivery routes, and observed therapeutic effects.
Main Results:
- Preclinical studies show pleiotropic benefits of cell transplantation, including improved myocardial remodeling, function, perfusion, and reduced fibrosis/inflammation.
- Observed benefits are largely attributed to the paracrine effects of transplanted stem cells promoting endogenous repair.
- Early human studies show modest and inconsistent, yet promising, results.
Conclusions:
- Cellular transplantation, particularly via stem cell paracrine mechanisms, offers a promising avenue for HF treatment.
- Key challenges and research questions remain to optimize cell therapy and integrate it into the HF management armamentarium.
Abstract:
The pathogenesis of cardiomyopathy and heart failure (HF) is underpinned by complex changes at subcellular, cellular and extracellular levels in the ventricular myocardium. For all of the gains that conventional treatments for HF have brought to mortality and morbidity, they do not adequately address the loss of cardiomyocyte numbers in the remodeling ventricle. Originally conceived to address this problem, cellular transplantation for HF has already gone through several stages of evolution over the past two decades. Various cell types and delivery routes have been implemented to positive effect in preclinical models of ischemic and nonischemic cardiomyopathy, with pleiotropic benefits observed in terms of myocardial remodeling, systolic and diastolic performance, perfusion, fibrosis, inflammation, metabolism and electrophysiology. To a large extent, these salubrious effects are now attributed to the indirect, paracrine capacity of transplanted stem cells to facilitate endogenous cardiac repair processes. Promising results have also followed in early phase human studies, although these have been relatively modest and somewhat inconsistent. This review details the preclinical and clinical evidence currently available regarding the use of pluripotent stem cells and adult-derived progenitor cells for cardiomyopathy and HF. It outlines the important lessons that have been learned to this point in time, and balances the promise of this exciting field against the key challenges and questions that still need to be addressed at all levels of research, to ensure that cell therapy realizes its full potential by adding to the armamentarium of HF management.
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