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 - Funding Information:
This work was supported by Projects for Technological Development, Research Center Network for Realization of Regenerative Medicine by Japan, the Japan Society for the Promotion of Science (JSPS) KAKENHI 20K17129 and 22K08164 to YK, and KAKENHI 20H05744 to ST.
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
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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 -