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- W2752877290 abstract "Adenovirus (Ad)-based vectors are efficient gene-transfer vehicles to deliver foreign DNA into living organisms, offering large cargo capacity and low immunogenicity and genotoxicity. As Ad shows low integration rates of their genomes into host chromosomes, vector-derived gene expression decreases due to continuous cell cycling in regenerating tissues and dividing cell populations. To overcome this hurdle, adenoviral delivery can be combined with mechanisms leading to maintenance of therapeutic DNA and long-term effects of the desired treatment. Several hybrid Ad vectors (AdV) exploiting various strategies for long-term treatment have been developed and characterized. This review summarizes recent developments of preclinical approaches using hybrid AdVs utilizing either the Sleeping Beauty transposase system for somatic integration into host chromosomes or designer nucleases, including transcription activator-like effector nucleases and clustered regularly interspaced short palindromic repeats/CRISPR-associated protein-9 nuclease for permanent gene editing. Further options on how to optimize these vectors further are discussed, which may lead to future clinical applications of these versatile gene-therapy tools." @default.
- W2752877290 created "2017-09-15" @default.
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- W2752877290 creator A5031086488 @default.
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- W2752877290 date "2017-10-01" @default.
- W2752877290 modified "2023-10-16" @default.
- W2752877290 title "Recent Advances in Preclinical Developments Using Adenovirus Hybrid Vectors" @default.
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- W2752877290 doi "https://doi.org/10.1089/hum.2017.140" @default.
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