Barr E, Carroll J, Kalynych A M, Tripathy S K, Kozarsky K, Wilson J M, Leiden J M
Department of Medicine, University of Chicago, IL 60637, USA.
Gene Ther. 1994 Jan;1(1):51-8.
The ability to express recombinant genes in the coronary vasculature and the myocardium holds promise for the treatment of a number of acquired and inherited cardiovascular diseases. Previous in vivo gene transfer approaches in the heart have been limited by relatively low efficiencies of gene transduction. In this report, we demonstrate that catheter-mediated infusion of replication-defective adenovirus into the coronary arterial circulation in vivo represents a novel and efficient method for the induction of recombinant gene expression in both the coronary arteries and the myocardium. A single intracoronary infusion of 2 x 10(9) - 1 x 10(10) p.f.u. of adenovirus resulted in high level recombinant gene expression in both the coronary arteries and surrounding myocardium of adult rabbits for at least 2 weeks. No inflammatory response or myocardial necrosis was observed following the adenovirus infusions. The polymerase chain reaction (PCR) was used to assess the tissue distribution of infection following intracoronary infusion of adenovirus. Adenovirus DNA was detected by PCR in the livers, kidneys, lungs, brains and testes of animals 5 days after virus infusion. Percutaneous transluminal gene transfer (PTGT) into the heart by intracoronary infusion of replication-defective adenovirus represents a relatively non-invasive and efficient method of inducing recombinant gene expression both in the coronary arterial wall and in the surrounding myocardium.
在冠状动脉血管系统和心肌中表达重组基因的能力为治疗多种获得性和遗传性心血管疾病带来了希望。以往心脏的体内基因转移方法受到基因转导效率相对较低的限制。在本报告中,我们证明,将复制缺陷型腺病毒通过导管介导注入体内的冠状动脉循环是一种在冠状动脉和心肌中诱导重组基因表达的新颖且有效的方法。单次冠状动脉内注入2×10⁹ - 1×10¹⁰ 个腺病毒空斑形成单位(p.f.u.)可使成年兔的冠状动脉和周围心肌中产生高水平的重组基因表达,持续至少2周。注入腺病毒后未观察到炎症反应或心肌坏死。采用聚合酶链反应(PCR)评估冠状动脉内注入腺病毒后的感染组织分布。病毒注入5天后,通过PCR在动物的肝脏、肾脏、肺、脑和睾丸中检测到腺病毒DNA。通过冠状动脉内注入复制缺陷型腺病毒进行经皮腔内基因转移(PTGT)至心脏是一种在冠状动脉壁和周围心肌中诱导重组基因表达的相对非侵入性且有效的方法。