Systematic Review of Genetic Substrate Reduction Therapy in Lysosomal Storage Diseases: Opportunities, Challenges and Delivery Systems.

IF 5.4 2区 医学 Q1 IMMUNOLOGY BioDrugs Pub Date : 2024-09-01 Epub Date: 2024-08-23 DOI:10.1007/s40259-024-00674-1
Marina Beraza-Millor, Julen Rodríguez-Castejón, Ana Del Pozo-Rodríguez, Alicia Rodríguez-Gascón, María Ángeles Solinís
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Abstract

Background: Genetic substrate reduction therapy (gSRT), which involves the use of nucleic acids to downregulate the genes involved in the biosynthesis of storage substances, has been investigated in the treatment of lysosomal storage diseases (LSDs).

Objective: To analyze the application of gSRT to the treatment of LSDs, identifying the silencing tools and delivery systems used, and the main challenges for its development and clinical translation, highlighting the contribution of nanotechnology to overcome them.

Methods: A systematic review following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) reporting guidelines was performed. PubMed, Scopus, and Web of Science databases were used for searching terms related to LSDs and gene-silencing strategies and tools.

Results: Fabry, Gaucher, and Pompe diseases and mucopolysaccharidoses I and III are the only LSDs for which gSRT has been studied, siRNA and lipid nanoparticles being the silencing strategy and the delivery system most frequently employed, respectively. Only in one recently published study was CRISPR/Cas9 applied to treat Fabry disease. Specific tissue targeting, availability of relevant cell and animal LSD models, and the rare disease condition are the main challenges with gSRT for the treatment of these diseases. Out of the 11 studies identified, only two gSRT studies were evaluated in animal models.

Conclusions: Nucleic acid therapies are expanding the clinical tools and therapies currently available for LSDs. Recent advances in CRISPR/Cas9 technology and the growing impact of nanotechnology are expected to boost the clinical translation of gSRT in the near future, and not only for LSDs.

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溶酶体储积症基因底物还原疗法系统综述:机遇、挑战和传输系统。
背景:基因底物还原疗法(gSRT)涉及使用核酸下调参与贮存物质生物合成的基因,已被研究用于治疗溶酶体贮积症(LSDs):分析 gSRT 在治疗溶酶体储积症中的应用,确定所用的沉默工具和传递系统,以及其开发和临床转化所面临的主要挑战,强调纳米技术在克服这些挑战方面的贡献:方法:按照系统综述和荟萃分析首选报告项目(PRISMA)报告指南进行了系统综述。使用 PubMed、Scopus 和 Web of Science 数据库检索与 LSDs 和基因沉默策略及工具相关的术语:法布里病、戈谢病、庞贝病以及粘多糖I型和III型粘多糖是唯一研究过gSRT的LSD,siRNA和脂质纳米颗粒分别是最常用的沉默策略和传递系统。只有在最近发表的一项研究中,CRISPR/Cas9 被用于治疗法布里病。特定的组织靶向、相关细胞和动物 LSD 模型的可用性以及罕见的疾病状况是 gSRT 治疗这些疾病的主要挑战。在已确定的 11 项研究中,只有两项 gSRT 研究在动物模型中进行了评估:结论:核酸疗法正在扩展目前可用于治疗 LSD 的临床工具和疗法。CRISPR/Cas9技术的最新进展和纳米技术日益增长的影响有望在不久的将来促进gSRT的临床转化,而且不仅仅针对LSDs。
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来源期刊
BioDrugs
BioDrugs 医学-免疫学
CiteScore
12.60
自引率
2.90%
发文量
50
审稿时长
>12 weeks
期刊介绍: An essential resource for R&D professionals and clinicians with an interest in biologic therapies. BioDrugs covers the development and therapeutic application of biotechnology-based pharmaceuticals and diagnostic products for the treatment of human disease. BioDrugs offers a range of additional enhanced features designed to increase the visibility, readership and educational value of the journal’s content. Each article is accompanied by a Key Points summary, giving a time-efficient overview of the content to a wide readership. Articles may be accompanied by plain language summaries to assist patients, caregivers and others in understanding important medical advances. The journal also provides the option to include various other types of enhanced features including slide sets, videos and animations. All enhanced features are peer reviewed to the same high standard as the article itself. Peer review is conducted using Editorial Manager®, supported by a database of international experts. This database is shared with other Adis journals.
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