Phielipp Nicolas, Henchcliffe Claire
Department of Neurology, University of California, 200 S. Manchester Avenue, Suite 206, Orange, CA, 92868, USA.
CNS Drugs. 2025 Jul 10. doi: 10.1007/s40263-025-01203-6.
Since the publication of the first gene therapy clinical trial in Parkinson's disease (PD) in 2007, rapid advances have resulted in escalating interest in applying this technology to manipulate various cellular processes altered in PD. There is now a rich literature describing the various approaches taken, including modulating aberrant networks, restoring dopamine, and mitigating deleterious effects of known gene mutations or as a restorative therapy. Evidence has accrued supporting feasibility, safety, and tolerability of initial gene therapy approaches, as well as providing initial indications of efficacy in several cases. However, there have also been unexpected challenges, and technology is still evolving, making this an important time point to evaluate what has been learned and to place it in context to support ongoing and future efforts. In this review, we focus on the potential of gene therapy to ameliorate symptoms and modify disease progression in PD. We critically review previous clinical research, we address potential benefits and predicted limitations, and we address pipeline approaches aiming to bring a gene therapy approach to the clinic.
自2007年帕金森病(PD)首个基因治疗临床试验公布以来,快速进展使得人们对应用该技术来调控PD中改变的各种细胞过程的兴趣不断增加。现在有大量文献描述了所采用的各种方法,包括调节异常网络、恢复多巴胺以及减轻已知基因突变的有害影响或作为一种恢复性疗法。已有证据支持初始基因治疗方法的可行性、安全性和耐受性,并在一些病例中提供了疗效的初步迹象。然而,也出现了意想不到的挑战,并且技术仍在不断发展,这使得这成为一个重要的时间点,来评估所学到的知识并将其置于背景中,以支持正在进行的和未来的努力。在这篇综述中,我们重点关注基因治疗改善PD症状和改变疾病进展的潜力。我们批判性地回顾以前的临床研究,探讨潜在益处和预计的局限性,并讨论旨在将基因治疗方法引入临床的在研方法。