Hidefumi Nishida, MD (left), and Takeyoshi Ota, MD, PhD (right)
Central Message.
Cardiac cellular reprogramming therapy is a rising technology to cope with heart failure. It still needs a breakthrough to expand clinical applications.
See Article page 108.
We congratulate Ryan and colleagues1 on their expert opinion regarding clinical potential of angiogenic therapy and cellular reprogramming. This article provides a current status and a future possibility of angiogenic therapy and cardiac cellular reprogramming to treat ischemic heart diseases.
Despite recent advancements in medicine and technology, ischemic heart disease is still one of the leading causes of death worldwide. The gold standard treatment strategies for severe ischemic heart disease are percutaneous catheter intervention or coronary artery bypass grafting on top of guideline-directed medical therapy.2 While these therapies have been proven to improve survival rates and quality of life in those patient populations, there are still limitations. In general, myocardial revascularization therapy helps to preserve the viable myocardium but does not contribute to restoring nonviable myocardium (ie, infarction). Infarcted myocardial tissues are eventually replaced with unfunctional fibrotic tissues, so-called maladaptive remodeling. Once ischemic heart diseases progress to the phase of maladaptive remodeling, the conventional revascularization with percutaneous catheter intervention/coronary artery bypass grafting is no longer helpful, since there is no target vasculature to revascularize. Transmyocardial revascularization was once expected as a promising technology to treat “nonviable” lesions; however, its efficacy was limited.3 A breakthrough in this field is needed.
Regenerative medicine has emerged in the last decade as a rising therapy for many fields. In this article, the authors describe the clinical potential of angiogenic therapy and cellular reprogramming for myocardial regeneration. Currently, there are 2 major approaches for myocardium regeneration. One is to use myocardial cells derived from induced pluripotent stem cell in vitro.4 This approach, however, raises some concerns, including poor engraftment rates, cost effectiveness, and the potential risk of tumorigenesis. The other approach is cellular reprogramming therapy.5 Damaged cardiomyocytes degenerate to fibroblast cells, which do not have any contractile function. By applying the transduction of cardiac-specific transcription factors into the fibroblast cells, those cells are converted to induced cardiomyocyte-like cells. The reprogramming technique uses intrinsic host cells to restore myocardium rather than allogeneic/xenogeneic transplantation, which could reduce a possible rejection reaction. It is also reported that there might be a synergic effect when the cardiac reprogramming technique is combined with angiogenic therapy.6 It could be a breakthrough and might facilitate clinical applications of cardiac cellular reprogramming technology.
It is true that there are a lot of challenges to overcome and further studies are warranted before generalized clinical use of these therapeutic technologies. However, we are hoping the technology broadens therapeutic options for patients suffering from severe ischemic heart disease. We appreciate for the authors giving us updated knowledge and deep insight about the current use of cardiac cellular reprogramming therapy.
Footnotes
Disclosures: The authors reported no conflicts of interest.
The Journal policy requires editors and reviewers to disclose conflicts of interest and to decline handling or reviewing manuscripts for which they may have a conflict of interest. The editors and reviewers of this article have no conflicts of interest.
References
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