Du Liang, Zhang Jingwan, De Meyer Guido R Y, Flynn Rowan, Dichek David A
1 Division of Cardiology, Department of Medicine, University of Washington , Seattle, WA 98195.
Hum Gene Ther Methods. 2014 Apr;25(2):106-14. doi: 10.1089/hgtb.2013.199. Epub 2014 Feb 14.
Gene therapy delivered to the blood vessel wall could augment current therapies for atherosclerosis, including systemic drug therapy and stenting. However, identification of clinically useful vectors and effective therapeutic transgenes remains at the preclinical stage. Identification of effective vectors and transgenes would be accelerated by availability of animal models that allow practical and expeditious testing of vessel-wall-directed gene therapy. Such models would include humanlike lesions that develop rapidly in vessels that are amenable to efficient gene delivery. Moreover, because human atherosclerosis develops in normal vessels, gene therapy that prevents atherosclerosis is most logically tested in relatively normal arteries. Similarly, gene therapy that causes atherosclerosis regression requires gene delivery to an existing lesion. Here we report development of three new rabbit models for testing vessel-wall-directed gene therapy that either prevents or reverses atherosclerosis. Carotid artery intimal lesions in these new models develop within 2-7 months after initiation of a high-fat diet and are 20-80 times larger than lesions in a model we described previously. Individual models allow generation of lesions that are relatively rich in either macrophages or smooth muscle cells, permitting testing of gene therapy strategies targeted at either cell type. Two of the models include gene delivery to essentially normal arteries and will be useful for identifying strategies that prevent lesion development. The third model generates lesions rapidly in vector-naïve animals and can be used for testing gene therapy that promotes lesion regression. These models are optimized for testing helper-dependent adenovirus (HDAd)-mediated gene therapy; however, they could be easily adapted for testing of other vectors or of different types of molecular therapies, delivered directly to the blood vessel wall. Our data also supports the promise of HDAd to deliver long-term therapy from vascular endothelium without accelerating atherosclerotic disease.
将基因疗法应用于血管壁可增强当前针对动脉粥样硬化的治疗方法,包括全身药物治疗和支架植入术。然而,临床上有用的载体和有效的治疗性转基因的鉴定仍处于临床前阶段。能够进行血管壁定向基因治疗的实用且快速测试的动物模型的出现,将加速有效载体和转基因的鉴定。此类模型应包括在易于进行高效基因传递的血管中迅速形成的类似人类的病变。此外,由于人类动脉粥样硬化在正常血管中发展,预防动脉粥样硬化的基因疗法最合理的测试方式是在相对正常的动脉中进行。同样,导致动脉粥样硬化消退的基因疗法需要将基因传递到现有的病变部位。在此,我们报告了三种用于测试血管壁定向基因治疗的新兔模型的开发,这些模型可预防或逆转动脉粥样硬化。在这些新模型中,颈动脉内膜病变在开始高脂饮食后的2至7个月内形成,比我们之前描述的模型中的病变大20至80倍。各个模型能够产生富含巨噬细胞或平滑肌细胞的病变,从而允许测试针对任一细胞类型的基因治疗策略。其中两个模型包括将基因传递到基本正常的动脉中,将有助于确定预防病变发展的策略。第三个模型在未接触载体的动物中迅速产生病变,可用于测试促进病变消退的基因治疗。这些模型经过优化,用于测试依赖辅助病毒的腺病毒(HDAd)介导的基因治疗;然而,它们可以很容易地适用于测试其他载体或直接应用于血管壁的不同类型分子疗法。我们的数据还支持HDAd从血管内皮提供长期治疗而不加速动脉粥样硬化疾病的前景。