Penn Marc S, Mangi Abeel A
Skirball Laboratory for Cardiovascular Cellular Therapeutics, Center for Cardiovascular Cellular Therapeutics, NE3, 9500 Euclid Avenue, Cleveland, OH 44195, USA.
Circ Res. 2008 Jun 20;102(12):1471-82. doi: 10.1161/CIRCRESAHA.108.175174.
Cell-based therapies for the prevention and treatment of cardiac dysfunction offer the potential to significantly modulate cardiac function and improve outcomes in patients with cardiovascular disease. To date several clinical studies have suggested the potential efficacy of several different stem cell types; however, the benefits seen in clinical trials have been inconsistent and modest. In parallel, preclinical studies have identified key events in the process of cell-based myocardial repair, including stem cell homing, engraftment, survival, paracrine factor release, and differentiation that need to be optimized to maximize cardiac repair and function. The inconsistent and modest benefits seen in clinical trials combined with the preclinical identification of mediators responsible for key events in cell-based cardiac repair offers the potential for cell-based therapy to advance to cell-based gene therapy in an attempt to optimize these key events in the hope of maximizing clinical benefit. Below we discuss potential key events in cardiac repair and the mediators of these events that could be of potential interest for genetic enhancement of stem cell-based cardiac repair.
用于预防和治疗心脏功能障碍的细胞疗法有望显著调节心脏功能并改善心血管疾病患者的预后。迄今为止,多项临床研究表明了几种不同干细胞类型的潜在疗效;然而,临床试验中观察到的益处并不一致且效果有限。与此同时,临床前研究已经确定了基于细胞的心肌修复过程中的关键事件,包括干细胞归巢、植入、存活、旁分泌因子释放以及分化,这些都需要优化以最大限度地实现心脏修复和功能改善。临床试验中观察到的益处不一致且效果有限,再加上临床前对基于细胞的心脏修复关键事件的介质的识别,使得基于细胞的疗法有可能发展为基于细胞的基因疗法,试图优化这些关键事件,以期最大限度地提高临床疗效。以下我们将讨论心脏修复中的潜在关键事件以及这些事件的介质,它们可能对基于干细胞的心脏修复的基因增强具有潜在意义。