期刊
NATURE BIOTECHNOLOGY
卷 28, 期 1, 页码 79-U107出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/nbt.1599
关键词
-
资金
- American Heart Association [0735637N]
- National Institute of Arthritis and Musculoskeletal and Skin Diseases [R21AR055712]
- National Institute of Allergy and Infectious Diseases [R01AI072176]
- National Heart, Lung, and Blood Institute [R01HL089221]
- Senator Paul Wellstone Center for Muscular Dystrophy [U54AR056953]
- National Institute of General Medical Sciences [R01GM082946]
Reengineering the receptor footprints of adeno-associated virus (AAV) isolates may yield variants with improved properties for clinical applications. We generated a panel of synthetic AAV2 vectors by replacing a hexapeptide sequence in a previously identified heparan sulfate receptor footprint with corresponding residues from other AAV strains. This approach yielded several chimeric capsids displaying systemic tropism after intravenous administration in mice. Of particular interest, an AAV2/AAV8 chimera designated AAV2i8 displayed an altered antigenic profile, readily traversed the blood vasculature, and selectively transduced cardiac and whole-body skeletal muscle tissues with high efficiency. Unlike other AAV serotypes, which are preferentially sequestered in the liver, AAV2i8 showed markedly reduced hepatic tropism. These features of AAV2i8 suggest that it is well suited to translational studies in gene therapy of musculoskeletal disorders.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据