Delivery of viral vectors for gene therapy in intimal hyperplasia and restenosis in atherosclerotic swine

被引:13
|
作者
Hall, Sannette [1 ]
Agrawal, Devendra K. [1 ,2 ]
机构
[1] Creighton Univ, Sch Med, Dept Clin & Translat Sci, Omaha, NE 68178 USA
[2] Creighton Univ, Dept Clin & Translat Sci, Sch Med, Med, CRISS 2 Room 510,2500 Calif Plaza, Omaha, NE 68178 USA
基金
美国国家卫生研究院;
关键词
Restenosis; Intimal hyperplasia; Viral vectors; Gene therapy; Porcinemodels; ENDOTHELIAL GROWTH-FACTOR; INHIBITS NEOINTIMAL FORMATION; IN-STENT RESTENOSIS; NITRIC-OXIDE; TISSUE INHIBITOR; CORONARY-ARTERY; ANIMAL-MODELS; LUMINAL LOSS; TGF-BETA; PREVENTION;
D O I
10.1007/s13346-017-0409-0
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
Cardiovascular diseases including atherosclerosis are a major financial and health burden globally. Inflammation associated with atherosclerosis results in the development of plaques that can rupture causing thrombosis, stroke, or death. The most widely used treatment for the removal of atherosclerotic plaques is percutaneous transluminal coronary angioplasty (PTCA) with or without stenting. Although this is a safer and minimally invasive method, restenosis and intimal hyperplasia after interventional procedure remains a major hurdle and more refined approaches are needed. Studies in large animal models such as pigs have facilitated a greater understanding of the underlying mechanisms of the disease and provided novel targets for therapeutic intervention. In pre-clinical studies, viral vector gene therapy has emerged as a promising option for the reduction and/or prevention of restenosis and intimal hyperplasia. Although studies in animal models have generated promising results, clinical trials have yet to prove the clinical efficacy of gene therapy in coronary artery diseases. In this review, we examined and critically reviewed the most recent advances in viral vector gene therapy obtained from studies using porcine model of atherosclerosis.
引用
收藏
页码:918 / 927
页数:10
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