Leontiadis E, Manginas A, Cokkinos D V
Heart Fail Rev. 2006 Jun;11(2):155-70. doi: 10.1007/s10741-006-9486-8.
Patients with ischemic cardiomyopathy have a poor prognosis despite all pharmacological, interventional and surgical treatment modalities currently applied. Heart transplantation remains the ideal treatment for this group of patients but the scarcity of donors hinders its widespread application. The autologous transplantation of stem cells (SCs) for cardiac repair is emerging as a new therapy for patients with myocardial dysfunction early after an acute infarction or ischemic cardiomyopathy. The rationale of this novel method is the enhancement of the repair mechanisms achieved by tissue-specific and circulating stem/progenitor cells. SCs assist naturally occurring myocardial repair by contributing to increased myocardial perfusion and contractile performance especially in the setting of acute myocardial infarction (AMI), but also in patients with chronic ischemic heart failure and advanced, diffuse coronary artery disease. The exact mechanism of their action has not been fully elucidated. Few studies continue to suggest a formation of few new contractile tissue. The majority if investigators believe that these cells do not persist long in the myocardium but that they secrete vascular growth and other cardioprotective factors.
尽管目前应用了所有的药物、介入和手术治疗方式,缺血性心肌病患者的预后仍然很差。心脏移植仍然是这类患者的理想治疗方法,但供体的稀缺阻碍了其广泛应用。自体干细胞移植用于心脏修复正成为急性心肌梗死或缺血性心肌病后早期心肌功能障碍患者的一种新疗法。这种新方法的基本原理是增强组织特异性和循环干细胞/祖细胞实现的修复机制。干细胞通过增加心肌灌注和改善收缩功能来协助自然发生的心肌修复,特别是在急性心肌梗死(AMI)的情况下,也适用于慢性缺血性心力衰竭和晚期弥漫性冠状动脉疾病患者。它们的确切作用机制尚未完全阐明。少数研究继续表明有少量新的收缩组织形成。大多数研究者认为这些细胞在心肌中不会长期存在,但它们会分泌血管生长因子和其他心脏保护因子。