mRNA therapeutics for central nervous system disorders

Q4 Pharmacology, Toxicology and Pharmaceutics Drug Delivery System Pub Date : 2022-07-25 DOI:10.2745/dds.37.247
Yuta Fukushima, K. Itaka
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Abstract

The high efficacy of mRNA COVID-19 vaccine encourages the wider application of mRNA therapeutics. Protein replacement therapy with mRNA therapeutics is a promising alternative DDS approach for administering trophic factor proteins in central nervous system disorders or enzyme replacement therapy in inherited enzyme deficient diseases. Although the concept to deliver the mRNA in vivo as a drug was demonstrated as early as 1990, mRNA instability hindered subsequent research development. The polymer-based carrier, polyplex nanomicelle, is a novel carrier for in vivo mRNA administration. Here, we introduce the researches of in vivo mRNA administration using the nanomicelle carrier to treat animal models, especially focusing on the central nervous system disorders including Alzheimer’s disease, spinal cord injury and ischemic brain disease. We discuss the advantages of mRNA therapeutics and the characteristics of diseases which are highly suitable for mRNA therapeutics. © 2022, Japan Society of Drug Delivery System. All rights reserved.
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mRNA治疗中枢神经系统疾病
mRNA新冠肺炎疫苗的高效性鼓励了mRNA疗法的更广泛应用。mRNA疗法的蛋白质替代疗法是一种很有前途的替代DDS方法,用于在中枢神经系统疾病中给予营养因子蛋白或在遗传性酶缺乏疾病中给予酶替代疗法。尽管早在1990年就已经证明了将信使核糖核酸作为药物在体内递送的概念,但信使核糖核酸的不稳定性阻碍了随后的研究发展。基于聚合物的载体,多聚体纳米胶束,是一种用于体内信使核糖核酸给药的新型载体。在这里,我们介绍了使用纳米胶束载体在体内给予信使核糖核酸治疗动物模型的研究,特别是关注中枢神经系统疾病,包括阿尔茨海默病、脊髓损伤和缺血性脑疾病。我们讨论了信使核糖核酸疗法的优势和高度适合信使核糖核酸治疗的疾病的特点。©2022,日本药物输送系统学会。保留所有权利。
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来源期刊
Drug Delivery System
Drug Delivery System Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
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