Bennett C Frank, Kordasiewicz Holly B, Cleveland Don W
Ionis Pharmaceuticals Inc., Carlsbad, California 92010, USA; email:
Ludwig Institute for Cancer Research and Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, California 92093, USA.
Annu Rev Pharmacol Toxicol. 2021 Jan 6;61:831-852. doi: 10.1146/annurev-pharmtox-010919-023738. Epub 2020 Oct 9.
The genetic basis for most inherited neurodegenerative diseases has been identified, yet there are limited disease-modifying therapies for these patients. A new class of drugs-antisense oligonucleotides (ASOs)-show promise as a therapeutic platform for treating neurological diseases. ASOs are designed to bind to the RNAs either by promoting degradation of the targeted RNA or by elevating expression by RNA splicing. Intrathecal injection into the cerebral spinal fluid results in broad distribution of antisense drugs and long-term effects. Approval of nusinersen in 2016 demonstrated that effective treatments for neurodegenerative diseases can be identified and that treatments not only slow disease progression but also improve some symptoms. Antisense drugs are currently in development for amyotrophic lateral sclerosis, Huntington's disease, Alzheimer's disease, Parkinson's disease, and Angelman syndrome, and several drugs are in late-stage research for additional neurological diseases. This review highlights the advances in antisense technology as potential treatments for neurological diseases.
大多数遗传性神经退行性疾病的遗传基础已被确定,但针对这些患者的疾病修饰疗法却很有限。一类新型药物——反义寡核苷酸(ASO)——有望成为治疗神经系统疾病的治疗平台。ASO旨在通过促进靶向RNA的降解或通过RNA剪接提高表达来与RNA结合。鞘内注射到脑脊液中可使反义药物广泛分布并产生长期效果。2016年,诺西那生钠获批,这表明可以找到治疗神经退行性疾病的有效疗法,而且这些疗法不仅能减缓疾病进展,还能改善一些症状。目前,反义药物正在针对肌萎缩侧索硬化症、亨廷顿舞蹈症、阿尔茨海默病、帕金森病和天使综合征进行研发,还有几种药物正处于针对其他神经系统疾病的后期研究阶段。这篇综述重点介绍了反义技术作为神经系统疾病潜在治疗方法的进展。