衣壳
基因传递
免疫系统
基因
遗传增强
病毒
计算生物学
生物
肽
病毒学
DNA
病毒载体
dna疫苗
输送系统
细胞生物学
生物信息学
神经系统
基因组
渗透(战争)
基因靶向
载体(分子生物学)
肽疫苗
化学
传染病(医学专业)
免疫反应
基因组编辑
作者
Charles W. Guo,Anastasia Diener,Shigemi Matsuyama
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2026-03-22
卷期号:18 (3): 395-395
标识
DOI:10.3390/pharmaceutics18030395
摘要
Adeno-associated viruses (AAVs) are a promising gene therapy technology, but major technical challenges remain. One problem is that commonly used AAVs have a low efficiency in penetrating the blood-brain barrier (BBB) and the blood-retina barrier (BRB). Consequently, gene delivery to the nervous system has limitations. Another problem is that AAVs induce immune reactions that cause serious side effects. To avoid immune reactions, the AAV dose must be reduced to lower levels that may result in insufficient gene delivery. Researchers have been modifying viral capsid protein sequences and searching for effective peptide sequences to solve these problems. As a result, Cell-Penetrating Penta-Peptides (CPP5s) have been shown to be effective in improving the BBB/BRB penetration of AAVs and suppressing immune reactions against AAVs. CPP5s were originally developed from peptide sequences of the Bax (a pro-apoptotic protein) binding domain of Ku70 (a DNA repair protein) and from negative control cell-penetrating peptides without Bax-binding activity. This article will discuss the background science of CPP5s and future directions of CPP5s for AAV-mediated gene delivery to the nervous system as well as other organs.
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