Cell and gene therapy for kidney disease

被引:27
|
作者
Peek, Jennifer L. [1 ,2 ]
Wilson, Matthew H. [2 ,3 ,4 ,5 ]
机构
[1] Vanderbilt Univ, Sch Med, Med Sci Training Program, Nashville, TN USA
[2] Vanderbilt Univ, Dept Cell & Dev Biol, 221 Kirkland Hall, Nashville, TN 37235 USA
[3] Vanderbilt Univ, Dept Pharmacol, 221 Kirkland Hall, Nashville, TN 37235 USA
[4] Vanderbilt Univ, Med Ctr, Dept Med, Div Nephrol & Hypertens, 221 Kirkland Hall, Nashville, TN 37235 USA
[5] Tennessee Valley Hlth Serv, Dept Vet Affairs, Nashville, TN 37235 USA
关键词
GLOMERULAR-BASEMENT-MEMBRANE; ENZYME REPLACEMENT THERAPY; RENAL-VEIN INJECTION; STEM-CELLS; VIRAL VECTORS; VSV-G; RECEPTOR; DELIVERY; EXPRESSION; GLOMERULONEPHRITIS;
D O I
10.1038/s41581-023-00702-3
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Kidney disease is a leading cause of morbidity and mortality across the globe. Current interventions for kidney disease include dialysis and renal transplantation, which have limited efficacy or availability and are often associated with complications such as cardiovascular disease and immunosuppression. There is therefore a pressing need for novel therapies for kidney disease. Notably, as many as 30% of kidney disease cases are caused by monogenic disease and are thus potentially amenable to genetic medicine, such as cell and gene therapy. Systemic disease that affects the kidney, such as diabetes and hypertension, might also be targetable by cell and gene therapy. However, although there are now several approved gene and cell therapies for inherited diseases that affect other organs, none targets the kidney. Promising recent advances in cell and gene therapy have been made, including in the kidney research field, suggesting that this form of therapy might represent a potential solution for kidney disease in the future. In this Review, we describe the potential for cell and gene therapy in treating kidney disease, focusing on recent genetic studies, key advances and emerging technologies, and we describe several crucial considerations for renal genetic and cell therapies.
引用
收藏
页码:451 / 462
页数:12
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