Division of Cardiovascular Surgery, Department of Surgery, University of Pennsylvania Medical Center, Philadelphia, PA 19104, USA.
Hum Gene Ther. 2010 Apr;21(4):371-80. doi: 10.1089/hum.2009.164.
Vector-mediated cardiac gene therapy holds tremendous promise as a translatable platform technology for treating many cardiovascular diseases. The ideal technique is one that is efficient and practical, allowing for global cardiac gene expression, while minimizing collateral expression in other organs. Here we survey the available in vivo vector-mediated cardiac gene delivery methods--including transcutaneous, intravascular, intramuscular, and cardiopulmonary bypass techniques--with consideration of the relative merits and deficiencies of each. Review of available techniques suggests that an optimal method for vector-mediated gene delivery to the large animal myocardium would ideally employ retrograde and/or anterograde transcoronary gene delivery,extended vector residence time in the coronary circulation, an increased myocardial transcapillary gradient using physical methods, increased endothelial permeability with pharmacological agents, minimal collateral gene expression by isolation of the cardiac circulation from the systemic, and have low immunogenicity.
载体介导的心脏基因治疗作为一种具有转化潜力的平台技术,有望治疗许多心血管疾病。理想的技术是高效且实用的,能够实现心脏基因的全局表达,同时最大限度地减少其他器官的旁系表达。在这里,我们调查了现有的体内载体介导的心脏基因传递方法,包括经皮、血管内、肌肉内和心肺旁路技术,同时考虑了每种方法的相对优缺点。对现有技术的回顾表明,对于将载体介导的基因递送至大型动物心肌的最佳方法,理想情况下应采用逆行和/或顺行冠状动脉基因递送、延长载体在冠状动脉循环中的停留时间、使用物理方法增加心肌跨毛细血管梯度、使用药理学方法增加内皮通透性、通过将心脏循环与全身循环隔离来最小化旁系基因表达,并且具有低免疫原性。