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[反义寡核苷酸作为神经遗传性疾病的新型疗法]

[Antisense oligonucleotide as novel therapies for neurogenetic disorders].

作者信息

Fan Liyuan

机构信息

University of Hong Kong Shenzhen Hospital, Shenzhen, Guangdong 518053, China.

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2025 Jan 10;42(1):102-113. doi: 10.3760/cma.j.cn511374-20240821-00451.

DOI:10.3760/cma.j.cn511374-20240821-00451
PMID:39779344
Abstract

Antisense oligonucleotide (ASO) was discovered several decades ago and initially used only as a research tool in the laboratory. In recent years, several ASO therapeutics have been developed for neurological disorders. Some of these therapeutics, including eteplirsen, golodirsen, viltolarsen, nusinersen and inotersen, have been approved by the Food and Drug Administration (FDA) and begun to draw the public's attention as an effective therapeutic approach. These novel therapeutics have shown great performance, while many similar therapeutics are under investigation and in clinical trials. This n-of-1 precision medicine may start a new chapter in the paradigm of therapeutics. Clinicians, clinical geneticists, and genetic counselors may know about this novel therapy, but very few may understand the background in details. During genetic counseling, they have the responsibility to convey the effectiveness, side effects and cost of such therapies to patients and their families. As these target therapies will require precise genetic diagnosis before treatment, healthcare professionals and genetic counselors play a vital role in relating the patients to the corresponding ASO drugs. This review has elaborated the mechanism of ASO therapies, including basic rationales, modifications, side effects and delivery routes. It also systemically summarized the FDA-approved ASO therapeutics and their applications for various neurological disorders, and discussed the limitations and challenges the real-world market may face and issues genetic counselor should take into consideration in the near future.

摘要

反义寡核苷酸(ASO)在几十年前就被发现了,最初仅在实验室用作研究工具。近年来,已经开发出几种用于治疗神经系统疾病的ASO疗法。其中一些疗法,包括依特普瑞森、戈洛迪森、维托拉森、诺西那生和伊诺特森,已获得美国食品药品监督管理局(FDA)批准,并开始作为一种有效的治疗方法引起公众关注。这些新型疗法表现出色,同时许多类似疗法正在研究和临床试验中。这种单病例精准医学可能会开启治疗模式的新篇章。临床医生、临床遗传学家和遗传咨询师可能了解这种新型疗法,但很少有人能详细了解其背景。在遗传咨询过程中,他们有责任向患者及其家属传达此类疗法的有效性、副作用和成本。由于这些靶向疗法在治疗前需要精确的基因诊断,医疗保健专业人员和遗传咨询师在将患者与相应的ASO药物联系起来方面发挥着至关重要的作用。本综述阐述了ASO疗法的机制,包括基本原理、修饰、副作用和给药途径。它还系统总结了FDA批准的ASO疗法及其在各种神经系统疾病中的应用,并讨论了现实市场可能面临的局限性和挑战,以及遗传咨询师在不久的将来应考虑的问题。

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[Antisense oligonucleotide as novel therapies for neurogenetic disorders].[反义寡核苷酸作为神经遗传性疾病的新型疗法]
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