发明公开
EP1597377A2 METHOD OF USING ADENOVIRAL VECTORS WITH INCREASED PERSISTENCE IN VIVO 审中-公开
腺病毒载体使用方法延长体内作用

METHOD OF USING ADENOVIRAL VECTORS WITH INCREASED PERSISTENCE IN VIVO
摘要:
The invention provides a method of expressing an exogenous nucleic acid in a mammal. The method comprises slowly releasing into the bloodstream a dose of replication-deficient or conditionally-replicating adenoviral vector having reduced ability to transduce mesothelial cells and hepatocytes. The normalized average bloodstream concentration of the adenovirus over 24 hours post-administration is at least about 1%. Alternatively, the normalized average bloodstream concentration over 24 hours post-administration is at least about 5-fold greater than the normalized average bloodstream concentration for an equivalent dose of a wild-type adenoviral vector. A method of destroying tumor cells in a mammal also is provided.
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