Adenoviral/lentiviral vectors for genetic modification

这项建议的广泛的长期目标是实现有针对性的，有效的和持久的基因转移到移植的心脏，并使用生物学相关基因的一氧化氮合酶（NOS）的亚型，以正常化冠状动脉血管反应性和减少心脏同种异体移植物血管病变（CAV）后，在一个小型和大型动物模型。该提议的中心假设是，使用独特的移植设置，可以实现心脏或心肌的血管的靶向、有效和持久的基因转导，并且可以通过用内皮或诱导型NOS（eNOS或iNOS）进行有效的心脏转导来减少心脏移植后冠状血管舒张的异常和CAV的发展。CAV是心脏移植后患者长期生存的最大障碍。基因治疗可以特别适用于移植的情况，因为供体器官在植入受体之前唯一可用于离体遗传修饰。在植入受体之前成功进行临床基因体外遗传修饰的主要挑战。成功的临床基因治疗的主要挑战包括需要最佳载体和递送系统来将遗传物质转移到体内组织。最近，第一次，基因递送到心脏的物理和化学条件已经显示允许载体选择性靶向心肌的冠状动脉的介质。使用常温灌注系统，移植前供体心脏的通常储存期可以转化为最佳基因递送期，而不影响移植物的活力。第一个目的是转化为一个最佳的基因输送期，而不影响移植物的活力。目前的建议的第一个目的是确定最合适的载体（腺病毒或慢病毒）和递送系统，使用化学修饰的常温灌注系统，在异位大鼠心脏移植模型中进行有效的，有针对性的和持久的基因递送。第二个目的是研究，使用最合适的载体和相同的传递系统从特定的目的1，eNOS或iNOS基因转移到冠状动脉血管或心肌的供体心脏对冠状动脉血管反应性和CAV异位猪心脏同种异体移植后的影响。将NOS作为选择的基因进行研究，因为降低的一氧化氮生物利用度是接受CAV的血管的特征。异常的内皮依赖性舒张先于冠状动脉萎缩，因此成功的NOS基因转移可能会影响疾病的早期阶段。在移植心脏的基因转移技术能够进展到临床之前，需要在大型动物模型中获得令人满意的经验。从生理学和病理学的角度来看，猪模型特别适合，也是未来临床异种移植的首选动物。成功实现这一建议的具体目标开辟了临床基因治疗的潜力，以避免心脏移植后的CAV。应用这些技术对非同种异体移植物动脉硬化的改变也有意义。

The broad long-term objectives of this proposal are to achieve targeted, efficient and durable gene transfer to the transplanted heart and, using biologically relevant genes for isoforms of nitric oxide synthase (NOS), to normalize coronary arterial vasoreactivity and reduce cardiac allograft vasculopathy (CAV) after allotransplantation in both a small and large animal model. The central hypotheses of this proposal are that, using the unique transplant setting, targeted, efficient and durable gene transduction of blood vessels of the heart or the myocardium can be achieved and that abnormalities in coronary vascular relaxation and the development of CAV after heart transplantation can be reduced by efficient cardiac transduction with endothelial or inducible NOS (eNOS or iNOS). CAV is the greatest obstacle to long-term patient survival after cardiac transplantation. Gene therapy may be particularly applicable in the setting of transplantation as the donor organ is uniquely available for genetic modification ex vivo prior to implantation into a recipient. Major challenges to successful clinical gene genetic modification ex vivo prior to implantation into a recipient. Major challenges to successful clinical gene therapy include the need for optimal vectors and delivery systems to transfer genetic material to tissues in vivo. Recently, for the first time, physical and chemical conditions of gene delivery to the heart have been shown to allow selective targeting of the vector to the media of the coronary arteries of the myocardium. Using a normothermic perfusion system, the usual period of storage of the donor heart before transplantation can be transformed into a period for optimal gene delivery without affecting the viability of the graft. The first aim of transformed into a period for optimal gene delivery without affecting the viability of the graft. The first aim of the current proposal is to identify the most suitable vector (adenovirus or lentivirus) and delivery system using chemical modification of a normothermic perfusion system for efficient, targeted and durable gene delivery in the heterotopic rat heart transplant model. The second aim is to study, using the most suitable vector and same delivery system from Specific Aim 1, the effects of eNOS or iNOS gene transfer to either the coronary vasculature or myocardium of the donor heart on coronary arterial vascular reactivity and on CAV after heterotopic pig heart allotransplantation. NOS will be studied as the gene of choice as reduced nitric oxide bioavailability is characteristic of vessels undergoing CAV. Abnormal endothelium dependent relaxation precedes CAV, so that successful NOS gene transfer might be expected to impact on the early stages of the disease. Before gene transfer technology to the transplanted heart can progress to the clinic, satisfactory experience in a large animal model will be necessary. The porcine model is particular suitable from a physiological and pathological viewpoint and is also the animal of choice for future clinical xenotransplantation. Success in achieving the specific aims of this proposal opens up the potential for clinical gene therapy to avoid CAV after heart transplantation. Implications also exist for the application of these techniques for the modification of non-allograft arteriosclerosis.