Cellivery R&D Institute, Cellivery Therapeutics, Inc., Seoul 07806, South Korea.
Cellivery R&D Institute, Cellivery Therapeutics, Inc., Seoul 07806, South Korea.
Pharmacol Res. 2024 Oct;208:107326. doi: 10.1016/j.phrs.2024.107326. Epub 2024 Jul 26.
Neurodegenerative disorders, such as Parkinson's disease (PD) and Alzheimer's disease (AD), have a global prevalence and profoundly impact both motor and cognitive functions. Although adeno-associated virus (AAV)-based gene therapy has shown promise, its application for treating central nervous system (CNS) diseases faces several challenges, including effective delivery of AAV vectors across the blood-brain barrier, determining optimal dosages, and achieving targeted distribution. To address these challenges, we have developed a fusion delivery therapeutic cargo called AAV-aMTD-Parkin, which combines a hydrophobic cell-penetrating peptide sequence with the DNA sequences of AAV and Parkin. By employing this fusion delivery platform at lower dosages compared to zolgensma, we have achieved significant enhancements in cell and tissue permeability, while reducing the occurrence of common pathological protein aggregates. Consequently, motor and cognitive functions were restored in animal models of PD and AD. With its dual functionality in addressing PD and AD, AAV-aMTD-Parkin holds immense potential as a novel class of therapeutic biologics for prevalent CNS diseases.
神经退行性疾病,如帕金森病 (PD) 和阿尔茨海默病 (AD),具有全球普遍性,严重影响运动和认知功能。尽管腺相关病毒 (AAV)- 为基础的基因治疗已显示出前景,但它在治疗中枢神经系统 (CNS) 疾病方面的应用面临着几个挑战,包括 AAV 载体穿过血脑屏障的有效传递、确定最佳剂量以及实现靶向分布。为了解决这些挑战,我们开发了一种融合传递治疗性货物的方法,称为 AAV-aMTD-Parkin,它将疏水性细胞穿透肽序列与 AAV 和 Parkin 的 DNA 序列结合在一起。与 zolgensma 相比,我们使用这种融合传递平台以较低的剂量,实现了细胞和组织通透性的显著增强,同时减少了常见的病理性蛋白聚集体的发生。因此,PD 和 AD 动物模型中的运动和认知功能得到了恢复。AAV-aMTD-Parkin 具有同时治疗 PD 和 AD 的双重功能,作为一种新型的治疗性生物制剂,它具有治疗常见 CNS 疾病的巨大潜力。