Summa Cardiovascular Institute, Summa Health System, Akron, OH, USA.
Gene Ther. 2012 Jun;19(6):583-7. doi: 10.1038/gt.2012.32.
Stem cell therapy for the prevention and treatment of cardiac dysfunction holds significant promise for patients with ischemic heart disease. Excitingly early clinical studies have demonstrated safety and some clinical feasibility, while at the same time studies in the laboratory have investigated mechanisms of action and strategies to optimize the effects of regenerative cardiac therapies. One of the key pathways that has been demonstrated critical in stem cell-based cardiac repair is (stromal cell-derived factor-1) SDF-1:CXCR4. SDF-1:CXCR4 has been shown to affect stem cell homing, cardiac myocyte survival and ventricular remodeling in animal studies of acute myocardial infarction and chronic heart failure. Recently released clinical data suggest that SDF-1 alone is sufficient to induce cardiac repair. Most importantly, studies like those on the SDF-1:CXCR4 axis have suggested mechanisms critical for cardiac regenerative therapies that if clinical investigators continue to ignore will result in poorly designed studies that will continue to yield negative results.
干细胞疗法在预防和治疗心脏功能障碍方面为缺血性心脏病患者带来了巨大的希望。令人兴奋的早期临床研究已经证明了其安全性和一定的临床可行性,同时实验室研究也探讨了作用机制和优化再生心脏治疗效果的策略。在基于干细胞的心脏修复中,一个被证明至关重要的关键途径是(基质细胞衍生因子-1)SDF-1:CXCR4。研究表明,SDF-1:CXCR4 可影响急性心肌梗死和慢性心力衰竭动物模型中的干细胞归巢、心肌细胞存活和心室重构。最近公布的临床数据表明,SDF-1 本身足以诱导心脏修复。最重要的是,像 SDF-1:CXCR4 轴这样的研究提示了心脏再生治疗的关键机制,如果临床研究人员继续忽视这些机制,将导致设计不佳的研究继续产生负面结果。