Mount Sinai School of Medicine, Department of Cardiology, New York, NY 10029-6574, USA.
Curr Vasc Pharmacol. 2013 Jul;11(4):465-79. doi: 10.2174/1570161111311040010.
Despite the great progress in cardiovascular health and clinical care along with marked decline in morbidity and mortality, cardiovascular diseases remain the leading causes of death and disability in the developed world. New therapeutic approaches, targeting not only systematic but also causal dysfunction, are ultimately needed to provide a valuable alternative for treatment of complex cardiovascular diseases. In heart failure, there are currently a number of trials that have been either completed or are ongoing targeting the sarcoplasmic reticulum calcium ATPase pump (SERCA2a) gene transfer in the context of heart failure. Recently, a phase 2 trial was completed, demonstrating safety and suggested benefit of adeno-associated virus type 1/SERCA2a gene transfer in advanced heart failure, supporting larger confirmatory trials. The experimental and clinical data suggest that, when administrated through perfusion, virus vector carrying SERCA2a can also transduce vascular endothelial and smooth muscle cells (EC and SMC) thereby improving the clinical benefit of gene therapy. Indeed, recent advances in understanding the molecular basis of vascular dysfunction point towards a reduction of sarcoplasmic reticulum Ca2+ uptake and an impairment of Ca2+ cycling in vascular EC and SMC from patients and preclinical models with cardiac diseases or with cardiovascular risk factors such as diabetes, hypercholesterolemia, coronary artery diseases, as well as other conditions such as pulmonary hypertension. In recent years, several studies have established that SERCA2a gene-based therapy could be an efficient option to treat vascular dysfunction. This review focuses on the recent finding showing the beneficial effects of SERCA2a gene transfer in vascular EC and SMC.
尽管心血管健康和临床护理取得了巨大进展,发病率和死亡率显著下降,但心血管疾病仍是发达国家死亡和残疾的主要原因。需要新的治疗方法,不仅针对系统性疾病,还针对因果性功能障碍,为治疗复杂心血管疾病提供有价值的替代方法。在心力衰竭中,目前有许多试验已经完成或正在进行,针对心力衰竭背景下的肌浆网钙 ATP 酶泵(SERCA2a)基因转移。最近,一项 2 期试验完成,证明了腺相关病毒 1/SERCA2a 基因转移在晚期心力衰竭中的安全性和有益性,支持更大规模的确认性试验。实验和临床数据表明,当通过灌注给药时,携带 SERCA2a 的病毒载体也可以转导血管内皮和平滑肌细胞(EC 和 SMC),从而提高基因治疗的临床获益。事实上,最近对血管功能障碍分子基础的理解进展表明,患有心脏病或心血管危险因素(如糖尿病、高胆固醇血症、冠状动脉疾病以及其他疾病如肺动脉高压)的患者和临床前模型的血管 EC 和 SMC 中的肌浆网 Ca2+摄取减少和 Ca2+循环受损。近年来,有几项研究已经证实,基于 SERCA2a 的基因治疗可能是治疗血管功能障碍的有效选择。这篇综述重点介绍了最近发现的 SERCA2a 基因转移对血管 EC 和 SMC 的有益影响。