Cardiovascular Research Center Mount Sinai School of Medicine, One Gustave L Levy Place, New York, NY 10029, USA.
Gene Ther. 2012 Jun;19(6):596-9. doi: 10.1038/gt.2012.34. Epub 2012 May 17.
Although progress in conventional treatments is making steady and incremental gains to reduce mortality associated with heart failure (HF), there remains a need to explore potentially new therapeutic approaches. HF induced by different etiologies such as coronary artery disease, hypertension, diabetes, infection or inflammation results generally in calcium cycling dysregulation at the myocyte level. Recent advances in understanding of the molecular basis of these calcium cycling abnormalities, together with the evolution of increasingly efficient gene transfer technology, has placed HF within the reach of gene-based therapy. Furthermore, the recent successful completion of a phase 2 trial targeting the sarcoplasmic reticulum calcium pump ushers in a new era for gene therapy for the treatment of HF.
尽管传统治疗方法的进展正在稳步取得增量收益,以降低与心力衰竭(HF)相关的死亡率,但仍需要探索潜在的新治疗方法。由不同病因引起的 HF,如冠状动脉疾病、高血压、糖尿病、感染或炎症,通常会导致心肌细胞水平的钙循环失调。对这些钙循环异常分子基础的理解的最新进展,以及基因转移技术的不断发展,使 HF 成为基因治疗的目标。此外,最近针对肌浆网钙泵的 2 期临床试验的成功完成,为 HF 的基因治疗开辟了一个新时代。