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RNA疗法:聚焦于神经系统中的反义寡核苷酸

RNA Therapeutics: Focus on Antisense Oligonucleotides in the Nervous System.

作者信息

Ertural Betül, Çiçek Büşra Nur, Kurnaz Işıl Aksan

机构信息

Gebze Technical University, Department of Molecular Biology and Genetics, 41400 Gebze Kocaeli, Turkiye.

Gebze Technical University, Institute of Biotechnology, 41400 Gebze Kocaeli, Turkiye.

出版信息

Biomol Ther (Seoul). 2025 Jun 19. doi: 10.4062/biomolther.2025.022.

Abstract

RNA therapeutics present a disruptive technology that has changed the drug discovery and manufacturing landscape, which established itself more prominently upon the recent COVID-19 pandemic. RNA therapeutics encompass diverse molecules like antisense oligonucleotides (ASOs), small interfering RNAs (siRNAs), microRNAs (miRNAs), RNA aptamers, and messenger RNAs (mRNAs), which can function through different mechanisms. RNA therapeutics are witnessing expanding applications across a range of diseases, notably in the treatment of neurological disorders. For instance, ASO therapies like nusinersen for spinal muscular atrophy and eteplirsen for Duchenne muscular dystrophy exemplify successful RNA therapeutic strategies. Emerging ASO treatments for Huntington's disease and amyotrophic lateral sclerosis are also promising, with ongoing clinical trials demonstrating significant reductions in disease-associated proteins. Still, delivery of these molecules remains a pivotal challenge in RNA therapeutics, especially for ASOs in penetrating the blood-brain barrier to target neurological disorders effectively. Nanoparticlebased formulations have emerged as leading strategies to enhance RNA stability, reduce immunogenicity, and improve cellular uptake. Despite these advances, significant hurdles remain, including optimizing pharmacokinetics, minimizing off-target effects, and ensuring sustained therapeutic efficacy. Regulatory frameworks are evolving to accommodate the unique challenges of RNAbased therapies, including ASOs with efforts underway to establish comprehensive guidelines for RNA therapeutics, yet there are also sustainable manufacturing issues that need to be considered for long-term feasibility. By addressing these challenges, RNA therapeutics hold immense potential to revolutionize treatment paradigms for neurological disorders. Looking forward, the future of RNA therapeutics in neurology appears promising but requires continued interdisciplinary collaboration and technological innovation.

摘要

RNA疗法是一项颠覆性技术,它改变了药物研发和制造格局,在近期的新冠疫情中其地位更加凸显。RNA疗法涵盖多种分子,如反义寡核苷酸(ASO)、小干扰RNA(siRNA)、微小RNA(miRNA)、RNA适配体和信使RNA(mRNA),它们可通过不同机制发挥作用。RNA疗法在一系列疾病中的应用不断拓展,尤其在神经系统疾病的治疗方面。例如,用于治疗脊髓性肌萎缩症的诺西那生和用于治疗杜氏肌营养不良症的依特普瑞森等ASO疗法就是成功的RNA治疗策略的典范。针对亨廷顿舞蹈症和肌萎缩侧索硬化症的新兴ASO疗法也很有前景,正在进行的临床试验表明疾病相关蛋白显著减少。然而,这些分子的递送仍是RNA疗法中的关键挑战,特别是对于ASO而言,要有效穿透血脑屏障以靶向神经系统疾病。基于纳米颗粒的制剂已成为增强RNA稳定性、降低免疫原性和改善细胞摄取的主要策略。尽管取得了这些进展,但仍存在重大障碍,包括优化药代动力学、最小化脱靶效应以及确保持续的治疗效果。监管框架正在不断发展以适应基于RNA疗法的独特挑战,包括针对ASO,目前正在努力为RNA疗法制定全面指南,但从长期可行性来看,还需要考虑可持续制造问题。通过应对这些挑战,RNA疗法在彻底改变神经系统疾病治疗模式方面具有巨大潜力。展望未来,RNA疗法在神经学领域的前景看似广阔,但仍需要持续的跨学科合作和技术创新。

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