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单基因疾病的质粒基因治疗:挑战与展望

Plasmid Gene Therapy for Monogenic Disorders: Challenges and Perspectives.

作者信息

Luís Marco A, Goes Marcelo A D, Santos Fátima Milhano, Mesquita Joana, Tavares-Ratado Paulo, Tomaz Cândida Teixeira

机构信息

CICS-UBI-Health Sciences Research Centre, University of Beira Interior, 6201-506 Covilhã, Portugal.

RISE-Health, Faculty of Sciences, University of Beira Interior, 6201-506 Covilhã, Portugal.

出版信息

Pharmaceutics. 2025 Jan 14;17(1):104. doi: 10.3390/pharmaceutics17010104.

Abstract

Monogenic disorders are a group of human diseases caused by mutations in single genes. While some disease-altering treatments offer relief and slow the progression of certain conditions, the majority of monogenic disorders still lack effective therapies. In recent years, gene therapy has appeared as a promising approach for addressing genetic disorders. However, despite advancements in gene manipulation tools and delivery systems, several challenges remain unresolved, including inefficient delivery, lack of sustained expression, immunogenicity, toxicity, capacity limitations, genomic integration risks, and limited tissue specificity. This review provides an overview of the plasmid-based gene therapy techniques and delivery methods currently employed for monogenic diseases, highlighting the challenges they face and exploring potential strategies to overcome these barriers.

摘要

单基因疾病是由单个基因突变引起的一组人类疾病。虽然一些改变疾病的治疗方法可以缓解症状并减缓某些疾病的进展,但大多数单基因疾病仍然缺乏有效的治疗方法。近年来,基因治疗已成为解决遗传疾病的一种有前景的方法。然而,尽管基因操作工具和递送系统取得了进展,但仍有几个挑战尚未解决,包括递送效率低下、缺乏持续表达、免疫原性、毒性、容量限制、基因组整合风险以及组织特异性有限。本文综述了目前用于单基因疾病的基于质粒的基因治疗技术和递送方法,强调了它们面临的挑战,并探索克服这些障碍的潜在策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ebf/11768343/c21f4a870128/pharmaceutics-17-00104-g001.jpg

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