a Molecular and Cellular Cardiology, Department of Medical and Surgical Sciences , Magna Graecia University , Catanzaro , Italy.
b Department of Cardiothoracic Sciences , University of Campania "L. Vanvitelli" , Naples , Italy.
Expert Opin Biol Ther. 2018 Apr;18(4):409-423. doi: 10.1080/14712598.2018.1430762. Epub 2018 Jan 24.
The characterization of multipotent endogenous cardiac stem cells (eCSCs) and the breakthroughs of somatic cell reprogramming to boost cardiomyocyte replacement have fostered the prospect of achieving functional heart repair/regeneration.
Allogeneic CSC therapy through its paracrine stimulation of the endogenous resident reparative/regenerative process produces functional meaningful myocardial regeneration in pre-clinical porcine myocardial infarction models and is currently tested in the first-in-man human trial. The in vivo test of somatic reprogramming and cardioregenerative non-coding RNAs revived the interest in gene therapy for myocardial regeneration. The latter, together with the advent of genome editing, has prompted most recent efforts to produce genetically-modified allogeneic CSCs that secrete cardioregenerative factors to optimize effective myocardial repair.
The current war against heart failure epidemics in western countries seeks to find effective treatments to set back the failing hearts prolonging human lifespan. Off-the-shelf allogeneic-genetically-modified CSCs producing regenerative agents are a novel and evolving therapy set to be affordable, safe, effective and available at all times for myocardial regeneration to either prevent or treat heart failure.
多能内源性心脏干细胞(eCSCs)的特征描述,以及体细胞重编程以促进心肌细胞替代的突破,为实现功能性心脏修复/再生的前景提供了希望。
同种异体 CSC 治疗通过旁分泌刺激内源性驻留修复/再生过程,在临床前猪心肌梗死模型中产生有意义的功能性心肌再生,目前正在首例人体试验中进行测试。体细胞重编程和心脏再生非编码 RNA 的体内试验重新激发了人们对心肌再生基因治疗的兴趣。后者,连同基因组编辑的出现,促使最近大多数努力产生分泌心脏再生因子的基因修饰同种异体 CSC,以优化有效的心肌修复。
目前西方国家与心力衰竭流行的斗争旨在寻找有效的治疗方法,延缓衰竭心脏,延长人类寿命。现成的同种异体基因修饰 CSC 产生再生剂是一种新颖且不断发展的治疗方法,旨在负担得起、安全、有效,并随时可用于心肌再生,以预防或治疗心力衰竭。