靶向α-突触核蛋白聚集免疫治疗:帕金森病的一种有前景的治疗方法

Gabriela Henríquez, M. Narayan
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引用次数: 0

摘要

帕金森病(PD)是一种流行的神经退行性疾病(NDD),影响着数百万人。PD的发病机制围绕着α-突触核蛋白(α-Syn),这是一种关键蛋白,其聚集显著影响疾病进展。尽管现有的治疗方法主要集中在通过靶向多巴胺能系统来控制运动症状,但它们经常忽视其他非运动症状。帕金森病发病机制的复杂性给疾病分析带来了挑战,并阻碍了有效的帕金森病治疗方法的发展。近年来,利用免疫疗法的各种新疗法在临床前动物模型中显示出了前景。在NDD中,免疫疗法旨在通过中和有毒物种并帮助其消除来抵消蛋白质积累的有害影响。针对帕金森病和相关突触核蛋白疾病,已经设计了许多主动治疗(AI)和被动免疫治疗(PI)策略,其中许多目前正在进行临床试验。尽管在动物模型中取得了显著成功,但免疫疗法在临床试验的后期遇到了实质性的挫折,除了lecanemab,它靶向阿尔茨海默病(AD)中的淀粉样蛋白-β(Aβ),最近获得了美国食品药品监督管理局(FDA)的批准。缺乏从实验研究到成功临床结果的转化,特别是在认知和功能评估方面,凸显了仅依靠动物研究来理解免疫治疗方法效果的局限性。这篇全面的综述聚焦于基于α-Syn的免疫疗法,并深入探讨其潜在的作用机制。此外,本文还讨论了PD免疫治疗策略潜力的最新进展和未来前景。重点是强调该领域的最新研究,以阐明开发有效的PD免疫疗法的挑战和机遇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting α-synuclein aggregation with immunotherapy: a promising therapeutic approach for Parkinson’s disease
Parkinson’s disease (PD) is a prevalent neurodegenerative disease (NDD) affecting millions of individuals. The pathogenesis of PD centers around α-synuclein (α-Syn), a pivotal protein whose aggregation significantly impacts disease progression. Although existing treatments mainly focus on managing motor symptoms by targeting the dopaminergic system, they frequently overlook other non-motor symptoms. The intricate nature of PD pathogenesis contributes to challenges in disease analysis and has hindered the development of effective PD treatments. In recent years, various novel therapies utilizing immunotherapy methods have exhibited promise in preclinical animal models. In NDDs, immunotherapy aims to counteract the detrimental effects of protein accumulation by neutralizing toxic species and aiding their elimination. Numerous active therapy (AI) and passive immunotherapy (PI) strategies have been devised for PD and related synucleinopathies, many of which are currently undergoing clinical trials. Despite demonstrating remarkable success in animal models, immunotherapies encountered substantial setbacks during the late stages of clinical trials, with the exception of lecanemab, which targets amyloid-β (Aβ) in Alzheimer’s disease (AD) and has recently received approval from the Food and Drug Administration (FDA). The lack of translation from experimental investigations to successful clinical outcomes, particularly in terms of cognitive and functional evaluations, highlights the limitations of relying solely on animal studies to comprehend the effects of immunotherapeutic approaches. This comprehensive review focuses on α-Syn-based immunotherapies and delves into their underlying mechanisms of action. Furthermore, Furthermore, the article discusses recent advancements and future prospects concerning the potential of immunotherapeutic strategies for PD. The focus is on highlighting the latest research in this domain to illuminate the challenges and opportunities related to the development of efficacious immunotherapies for individuals with PD.
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