Mandel Ronald J, Burger Corinna, Snyder Richard O
Department of Neuroscience, University of Florida College of Medicine, Gainesville, FL 32610, USA.
Exp Neurol. 2008 Jan;209(1):58-71. doi: 10.1016/j.expneurol.2007.08.008. Epub 2007 Aug 24.
Because Parkinson's disease is a progressive degenerative disorder that is mainly confined to the basal ganglia, gene transfer to deliver therapeutic molecules is an attractive treatment avenue. The present review focuses on direct in vivo gene transfer vectors that have been developed to a degree that they have been successfully used in animal model of Parkinson's disease. Accordingly, the properties of recombinant adenovirus, recombinant adeno-associated virus, herpes simplex virus, and lentivirus are described and contrasted. In order for viral vectors to be developed into clinical grade reagents, they must be manufactured and tested to precise regulatory standards. Indeed, clinical lots of viral vectors can be produced in compliance with current Good Manufacturing Practices (cGMPs) regulations using industry accepted manufacturing methodologies, manufacturing controls, and quality systems. The viral vector properties themselves combined with physiological product formulations facilitate long-term storage and direct in vivo administration.
由于帕金森病是一种主要局限于基底神经节的进行性退行性疾病,通过基因转移来递送治疗分子是一种有吸引力的治疗途径。本综述聚焦于已发展到一定程度并成功应用于帕金森病动物模型的直接体内基因转移载体。因此,对重组腺病毒、重组腺相关病毒、单纯疱疹病毒和慢病毒的特性进行了描述和对比。为了将病毒载体开发成临床级试剂,必须按照精确的监管标准进行生产和测试。事实上,临床批次的病毒载体可以使用业界认可的生产方法、生产控制和质量体系,按照现行良好生产规范(cGMP)法规进行生产。病毒载体的特性与生理性产品配方相结合,便于长期储存和直接体内给药。