Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
Batavia Biosciences B.V., Bioscience Park Leiden, Zernikedreef 16, 2333, CL, Leiden, The Netherlands.
J Mol Med (Berl). 2022 Jun;100(6):875-901. doi: 10.1007/s00109-022-02208-0. Epub 2022 May 24.
Despite the development of novel pharmacological treatments, cardiovascular disease morbidity and mortality remain high indicating an unmet clinical need. Viral gene therapy enables targeted delivery of therapeutic transgenes and represents an attractive platform for tackling acquired and inherited cardiovascular diseases in the future. Current cardiovascular gene therapy trials in humans mainly focus on improving cardiac angiogenesis and function. Encouragingly, local delivery of therapeutic transgenes utilising first-generation human adenovirus serotype (HAd)-5 is safe in the short term and has shown some efficacy in drug refractory angina pectoris and heart failure with reduced ejection fraction. Despite this success, systemic delivery of therapeutic HAd-5 vectors targeting cardiovascular tissues and internal organs is limited by negligible gene transfer to target cells, elimination by the immune system, liver sequestration, off-target effects, and episomal degradation. To circumvent these barriers, cardiovascular gene therapy research has focused on determining the safety and efficacy of rare alternative serotypes and/or genetically engineered adenoviral capsid protein-modified vectors following local or systemic delivery. Pre-clinical studies have identified several vectors including HAd-11, HAd-35, and HAd-20-42-42 as promising platforms for local and systemic targeting of vascular endothelial and smooth muscle cells. In the past, clinical gene therapy trials were often restricted by limited scale-up capabilities of gene therapy medicinal products (GTMPs) and lack of regulatory guidance. However, significant improvement of industrial GTMP scale-up and purification, development of novel producer cell lines, and issuing of GTMP regulatory guidance by national regulatory health agencies have addressed many of these challenges, creating a more robust framework for future adenoviral-based cardiovascular gene therapy. In addition, this has enabled the mass roll out of adenovirus vector-based COVID-19 vaccines. KEY MESSAGES: First-generation HAd-5 vectors are widely used in cardiovascular gene therapy. HAd-5-based gene therapy was shown to lead to cardiac angiogenesis and improved function. Novel HAd vectors may represent promising transgene carriers for systemic delivery. Novel methods allow industrial scale-up of rare/genetically altered Ad serotypes. National regulatory health agencies have issued guidance on GMP for GTMPs.
尽管新型药理学治疗方法不断发展,但心血管疾病的发病率和死亡率仍然居高不下,这表明临床需求尚未得到满足。病毒基因治疗可实现治疗性转基因的靶向递送,代表了未来治疗获得性和遗传性心血管疾病的一种有吸引力的平台。目前,人体心血管基因治疗试验主要集中在改善心脏血管生成和功能上。令人鼓舞的是,第一代人腺病毒血清型(HAd)-5 的局部转导治疗基因在短期内是安全的,并在药物难治性心绞痛和射血分数降低的心力衰竭中显示出一定的疗效。尽管取得了这一成功,但针对心血管组织和内脏器官的治疗性 HAd-5 载体的全身递送受到向靶细胞转移基因的能力极低、免疫系统消除、肝脏隔离、脱靶效应和外显子降解的限制。为了克服这些障碍,心血管基因治疗研究集中在确定局部或全身递送后罕见替代血清型和/或基因工程腺病毒衣壳蛋白修饰载体的安全性和有效性。临床前研究已经确定了几种载体,包括 HAd-11、HAd-35 和 HAd-20-42-42,作为局部和全身靶向血管内皮和平滑肌细胞的有前途的平台。过去,临床基因治疗试验通常受到基因治疗药物(GTMP)规模扩大能力有限和缺乏监管指导的限制。然而,国家监管健康机构对 GTMP 规模扩大和纯化的显著改进、新型生产细胞系的开发以及 GTMP 监管指导的发布,解决了许多这些挑战,为未来基于腺病毒的心血管基因治疗创造了更强大的框架。此外,这使得基于腺病毒载体的 COVID-19 疫苗得以大规模推出。 主要信息:第一代 HAd-5 载体广泛用于心血管基因治疗。基于 HAd-5 的基因治疗可导致心脏血管生成和功能改善。新型 HAd 载体可能代表系统递送有前途的转基因载体。新型方法允许稀有/基因改变的 Ad 血清型的工业规模扩大。国家监管健康机构发布了 GTMP 的 GMP 指南。