Molecular signatures of disease brain endothelia provide new sites for CNS-directed enzyme therapy

被引:137
作者
Chen, Yong Hong [1 ]
Chang, Michael [2 ]
Davidson, Beverly L. [1 ,2 ,3 ]
机构
[1] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Mol Physiol & Biophys, Iowa City, IA 52242 USA
[3] Univ Iowa, Dept Neurol, Iowa City, IA 52242 USA
基金
美国国家卫生研究院;
关键词
NEURONAL CEROID-LIPOFUSCINOSIS; ADENOASSOCIATED VIRUS; MOUSE MODEL; GENE; EVOLUTION; VECTORS; PHENOTYPES; LIBRARIES; TROPISM;
D O I
10.1038/nm.2025
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
The brain vasculature forms an immense network such that most neural cells are in contact with a microvessel. Here we tested the hypothesis that endothelia lining these vessels can be harnessed to create a cellular reservoir of enzyme replacement therapy to diseased brain. As a model system, we used mice with central nervous system (CNS) deficits due to lysosomal storage disease (LSD mice). The basic premise of this work is that recombinant enzyme expressed in, and secreted from, the vascular endothelia will be endocytosed by underlying neurons and glia, decreasing neuropathology. We screened a phage library in vivo by panning to identify peptides that bound the vascular endothelia in diseased and wild-type mice. Epitopes binding diseased brain were distinct from those panned from normal brain. Moreover, different epitopes were identified in two distinct LSD disease models, implying a unique vascular signature imparted by the disease state. Presentation of these epitopes on the capsid of adeno-associated virus (AAV) expanded the biodistribution of intravenously injected AAV from predominantly liver to include the CNS. Peripheral injection of the epitope-modified AAVs expressing the enzymes lacking in LSD mice reconstituted enzyme activity throughout the brain and improved disease phenotypes in two distinct disease models.
引用
收藏
页码:1215 / U145
页数:5
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