The potential of RNA-based therapy for kidney diseases

被引:24
作者
Bondue, Tjessa [1 ,2 ]
van den Heuvel, Lambertus [1 ,2 ,3 ]
Levtchenko, Elena [1 ,2 ]
Brock, Roland [4 ,5 ]
机构
[1] Univ Hosp Leuven, Dept Dev & Regenerat, UZ Herestr 49, B-3000 Leuven, Belgium
[2] Katholieke Univ Leuven, UZ Herestr 49, B-3000 Leuven, Belgium
[3] Radboud Univ Nijmegen, Dept Pediat Nephrol, Med Ctr, Nijmegen, Netherlands
[4] Radboud Univ Nijmegen, Med Ctr, Dept Biochem, Radboud Inst Mol Life Sci, Geert Grootepl 28, NL-6525 GA Nijmegen, Netherlands
[5] Arabian Gulf Univ, Coll Med & Med Sci, Dept Med Biochem, Manama, Bahrain
关键词
RNA; Kidney disease; RNA-therapy; Nanoparticles; SMALL INTERFERING RNA; MESSENGER-RNA; TARGETED DELIVERY; DRUG-DELIVERY; IN-VITRO; CHITOSAN/SIRNA NANOPARTICLES; PROTECTS MICE; SIRNA; PEPTIDE; RECEPTOR;
D O I
10.1007/s00467-021-05352-w
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Inherited kidney diseases (IKDs) are a large group of disorders affecting different nephron segments, many of which progress towards kidney failure due to the absence of curative therapies. With the current advances in genetic testing, the understanding of the molecular basis and pathophysiology of these disorders is increasing and reveals new potential therapeutic targets. RNA has revolutionized the world of molecular therapy and RNA-based therapeutics have started to emerge in the kidney field. To apply these therapies for inherited kidney disorders, several aspects require attention. First, the mRNA must be combined with a delivery vehicle that protects the oligonucleotides from degradation in the blood stream. Several types of delivery vehicles have been investigated, including lipid-based, peptide-based, and polymer-based ones. Currently, lipid nanoparticles are the most frequently used formulation for systemic siRNA and mRNA delivery. Second, while the glomerulus and tubules can be reached by charge- and/or size-selectivity, delivery vehicles can also be equipped with antibodies, antibody fragments, targeting peptides, carbohydrates or small molecules to actively target receptors on the proximal tubule epithelial cells, podocytes, mesangial cells or the glomerular endothelium. Furthermore, local injection strategies can circumvent the sequestration of RNA formulations in the liver and physical triggers can also enhance kidney-specific uptake. In this review, we provide an overview of current and potential future RNA-based therapies and targeting strategies that are in development for kidney diseases, with particular interest in inherited kidney disorders.
引用
收藏
页码:327 / 344
页数:18
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