Gene therapy and kidney diseases

被引:2
|
作者
Tavakolidakhrabadi, Nadia [1 ]
Ding, Wen Y. [1 ]
Saleem, Moin A. [1 ,2 ]
Welsh, Gavin I. [1 ]
May, Carl [1 ]
机构
[1] Univ Bristol, Bristol Renal, Dorothy Hodgkin Bldg,Whitson St, Bristol BS1 3NY, England
[2] Univ Hosp Bristol & Weston NHS Fdn Trust, Bristol Royal Hosp Children, Dept Paediat Nephrol, Upper Maudlin St, Bristol BS2 8BJ, England
关键词
EXTRACELLULAR-MATRIX ACCUMULATION; MESANGIAL CELL VECTOR; IN-VIVO; CHITOSAN/SIRNA NANOPARTICLES; TARGETED MUTATION; RENAL GLOMERULUS; NONVIRAL VECTOR; DOWN-REGULATION; RAT GLOMERULUS; VEHICLE CELLS;
D O I
10.1016/j.omtm.2024.101333
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Chronic kidney disease (CKD) poses a significant global health challenge, projected to become one of the leading causes of death by 2040. Current treatments primarily manage complications and slow progression, highlighting the urgent need for personalized therapies targeting the disease-causing genes. Our increased understanding of the underlying genomic changes that lead to kidney diseases coupled with recent successful gene therapies targeting specific kidney cells have turned gene therapy and genome editing into a promising therapeutic approach for treating kidney disease. This review paper reflects on different delivery routes and systems that can be exploited to target specific kidney cells and the ways that gene therapy can be used to improve kidney health.
引用
收藏
页数:24
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