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Pluripotent Stem Cell Derived Cardiac Cells for Myocardial Repair
Published on: February 3, 2017
Concise Review: Optimized Strategies for Stem Cell-Based Therapy in Myocardial Repair: Clinical Translatability and
Rongrong Wu1,2, Xinyang Hu1,2, Jian'an Wang1,2
1Department of Cardiology, Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, People's Republic of China.
Insights
Stem cell therapy shows promise for repairing heart damage from ischemic heart diseases (IHDs). This review compares cell types, delivery methods, and optimization strategies for successful clinical translation.
Area of Science:
- Regenerative Medicine
- Cardiovascular Research
- Stem Cell Biology
Background:
- Ischemic heart diseases (IHDs) cause significant cardiomyocyte loss, with current treatments limited in reversing damage.
- Stem cell therapy has emerged as a potential strategy for cardiac repair and functional recovery following IHDs.
- Despite promising preclinical data, clinical translation of stem cell therapy for IHDs faces skepticism due to inconsistent trial outcomes.
Purpose of the Study:
- To review and compare the efficacy of different stem cell types, dosages, delivery routes, and timing in preclinical and clinical settings for IHDs.
- To discuss the mechanisms of action of stem cells in myocardial repair, including the role of stem cell-derived secretomes and exosomes.
- To critically evaluate strategies for optimizing stem cells and cardiac microenvironments to improve engraftment and therapeutic efficacy for clinical application.
Main Methods:
- Comprehensive review of preclinical animal studies and clinical trials on stem cell therapy for IHDs.
- Analysis of stem cell types, including dose, delivery routes, and timing.
- Exploration of stem cell mechanisms, secretomes, and exosomes in myocardial repair.
- Evaluation of strategies to enhance stem cell engraftment and efficacy.
Main Results:
- Varied outcomes reported for different stem cell types, doses, and delivery methods in IHD treatment.
- Stem cell secretomes and exosomes play a significant role in mediating myocardial repair.
- Optimization of donor cells and cardiac microenvironments can enhance stem cell efficacy.
Conclusions:
- Stem cell therapy holds potential for treating IHDs, but further research is needed to address clinical translation challenges.
- Understanding stem cell mechanisms and optimizing delivery strategies are crucial for improving therapeutic outcomes.
- Future efforts should focus on enhancing stem cell engraftment and efficacy within the cardiac microenvironment for successful clinical application.
Abstract:
Ischemic heart diseases (IHDs) remain major public health problems with high rates of morbidity and mortality worldwide. Despite significant advances, current therapeutic approaches are unable to rescue the extensive and irreversible loss of cardiomyocytes caused by severe ischemia. Over the past 16 years, stem cell-based therapy has been recognized as an innovative strategy for cardiac repair/regeneration and functional recovery after IHDs. Although substantial preclinical animal studies using a variety of stem/progenitor cells have shown promising results, there is a tremendous degree of skepticism in the clinical community as many stem cell trials do not confer any beneficial effects. How to accelerate stem cell-based therapy toward successful clinical application attracts considerate attention. However, many important issues need to be fully addressed. In this Review, we have described and compared the effects of different types of stem cells with their dose, delivery routes, and timing that have been routinely tested in recent preclinical and clinical findings. We have also discussed the potential mechanisms of action of stem cells, and explored the role and underlying regulatory components of stem cell-derived secretomes/exosomes in myocardial repair. Furthermore, we have critically reviewed the different strategies for optimizing both donor stem cells and the target cardiac microenvironments to enhance the engraftment and efficacy of stem cells, highlighting their clinical translatability and potential limitation. Stem Cells 2018;36:482-500.
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