DIRECT GENE-TRANSFER OF HUMAN CFTR INTO HUMAN BRONCHIAL EPITHELIA OF XENOGRAFTS WITH E1-DELETED ADENOVIRUSES

被引:281
作者
ENGELHARDT, JF
YANG, YP
STRATFORDPERRICAUDET, LD
ALLEN, ED
KOZARSKY, K
PERRICAUDET, M
YANKASKAS, JR
WILSON, JM
机构
[1] UNIV MICHIGAN,DEPT INTERNAL MED,ANN ARBOR,MI 48109
[2] UNIV MICHIGAN,DEPT BIOL CHEM,ANN ARBOR,MI 48109
[3] INST GUSTAVE ROUSSY,CNRS,UA 1301,F-94805 VILLEJUIF,FRANCE
[4] UNIV N CAROLINA,DIV PULM DIS,CHAPEL HILL,NC 27599
[5] WISTAR INST ANAT & BIOL,INST HUMAN GENE THERAPY,PHILADELPHIA,PA 19104
关键词
D O I
10.1038/ng0593-27
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We describe the use of a human bronchial xenograft model for studying the efficiency and biology of in vivo gene transfer into human bronchial epithelia with recombinant E1 deleted adenoviruses. All cell types in the surface epithelium except basal cells efficiently expressed the adenoviral transduced recombinant genes, lacZ and CFTR, for 3-5 weeks. Stable transgene expression was associated with high level expression of the early adenoviral gene, E2a, in a subset of transgene expressing cells and virtually undetectable expression of the late adenoviral genes encoding the structural proteins, hexon and fiber. These studies begin to address important issues that relate to safety and in vivo efficacy of recombinant adenoviruses for gene delivery into the human airway.
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页码:27 / 34
页数:8
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