Gene therapy for monogenic disorders: challenges, strategies, and perspectives

被引:14
作者
Zhang, Yi [1 ,2 ,3 ,4 ]
Wu, Zhi-Ying [1 ,2 ,3 ,4 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 2, Dept Med Genet, Sch Med, Hangzhou 310009, Zhejiang, Peoples R China
[2] Zhejiang Univ, Affiliated Hosp 2, Ctr Rare Dis, Sch Med, Hangzhou 310009, Zhejiang, Peoples R China
[3] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Neurol, Hangzhou 310009, Zhejiang, Peoples R China
[4] Key Lab Med Neurobiol Zhejiang Prov, Hangzhou 310009, Zhejiang, Peoples R China
关键词
Gene therapy; Monogenic diseases; Gene editing; Gene delivery; Challenges; ADENOASSOCIATED VIRUS VECTOR; IN-VIVO DELIVERY; MOUSE MODEL; ALS; ACCUMULATION; EFFICACY; DISEASE; C9ORF72; TRIAL; FTD;
D O I
10.1016/j.jgg.2023.08.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Monogenic disorders refer to a group of human diseases caused by mutations in single genes. While disease -modifying therapies have offered some relief from symptoms and delayed progression for some monogenic diseases, most of these diseases still lack effective treatments. In recent decades, gene therapy has emerged as a promising therapeutic strategy for genetic disorders. Researchers have developed various gene manipulation tools and gene delivery systems to treat monogenic diseases. Despite this progress, concerns about inefficient delivery, persistent expression, immunogenicity, toxicity, capacity limitation, genomic integration, and limited tissue specificity still need to be addressed. This review gives an overview of commonly used gene therapy and delivery tools, along with the challenges they face and potential strategies to counter them. Copyright (c) 2023, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, and Genetics Society of China. Published by Elsevier Limited and Science Press. All rights reserved.
引用
收藏
页码:133 / 143
页数:11
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