TY - JOUR
T1 - Cardiac Regenerative Therapy Using Human Pluripotent Stem Cells for Heart Failure
T2 - A State-of-the-Art Review
AU - KISHINO, YOSHIKAZU
AU - TOHYAMA, SHUGO
AU - MORITA, YUIKA
AU - SOMA, YUSUKE
AU - TANI, HIDENORI
AU - OKADA, MARINA
AU - KANAZAWA, HIDEAKI
AU - FUKUDA, KEIICHI
N1 - Publisher Copyright:
© 2023 Elsevier Inc.
PY - 2023/4
Y1 - 2023/4
N2 - Heart transplantation (HT) is the only definitive treatment available for patients with end-stage heart failure who are refractory to medical and device therapies. However, HT as a therapeutic option, is limited by a significant shortage of donors. To overcome this shortage, regenerative medicine using human pluripotent stem cells (hPSCs), such as human embryonic stem cells and human-induced pluripotent stem cells (hiPSCs), has been considered an alternative to HT. Several issues, including the methods of large-scale culture and production of hPSCs and cardiomyocytes, the prevention of tumorigenesis secondary to contamination of undifferentiated stem cells and non-cardiomyocytes, and the establishment of an effective transplantation strategy in large-animal models, need to be addressed to fulfill this unmet need. Although post-transplantation arrhythmia and immune rejection remain problems, the ongoing rapid technological advances in hPSC research have been directed toward the clinical application of this technology. Cell therapy using hPSC-derived cardiomyocytes is expected to serve as an integral component of realistic medicine in the near future and is being potentially viewed as a treatment that would revolutionize the management of patients with severe heart failure.
AB - Heart transplantation (HT) is the only definitive treatment available for patients with end-stage heart failure who are refractory to medical and device therapies. However, HT as a therapeutic option, is limited by a significant shortage of donors. To overcome this shortage, regenerative medicine using human pluripotent stem cells (hPSCs), such as human embryonic stem cells and human-induced pluripotent stem cells (hiPSCs), has been considered an alternative to HT. Several issues, including the methods of large-scale culture and production of hPSCs and cardiomyocytes, the prevention of tumorigenesis secondary to contamination of undifferentiated stem cells and non-cardiomyocytes, and the establishment of an effective transplantation strategy in large-animal models, need to be addressed to fulfill this unmet need. Although post-transplantation arrhythmia and immune rejection remain problems, the ongoing rapid technological advances in hPSC research have been directed toward the clinical application of this technology. Cell therapy using hPSC-derived cardiomyocytes is expected to serve as an integral component of realistic medicine in the near future and is being potentially viewed as a treatment that would revolutionize the management of patients with severe heart failure.
KW - Regenerative medicine
KW - cardiomyocyte transplantation
KW - induced pluripotent stem cells
UR - http://www.scopus.com/inward/record.url?scp=85152095155&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85152095155&partnerID=8YFLogxK
U2 - 10.1016/j.cardfail.2022.10.433
DO - 10.1016/j.cardfail.2022.10.433
M3 - Review article
C2 - 37059512
AN - SCOPUS:85152095155
SN - 1071-9164
VL - 29
SP - 503
EP - 513
JO - Journal of Cardiac Failure
JF - Journal of Cardiac Failure
IS - 4
ER -