RCA-free production of third generation adenoviral vectors
نویسندگان
چکیده
Adenoviruses (Ad) have a long history as DNA-transfer vehicles in various medical applications including vivo gene therapy [1]. In this context, the favorable safety profile of Ad has been considered major benefit, since lack integration into host cell genome eliminates potential risks associated with insertional mutagenesis. This is combined comparatively high packaging capacity for foreign DNA, which relevant projects where therapeutic expression cassette too large other vectors such adeno-associated viruses. Further advantages include infectivity, high-titer virus production, excellent stability, and broad tissue tropism. 
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ژورنال
عنوان ژورنال: Cell & gene therapy insights
سال: 2022
ISSN: ['2059-7800', '2397-0545']
DOI: https://doi.org/10.18609/cgti.2022.215