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  • The successful use of any adenoviral vectors is predicated upon the use of a serotype that is not neutralized by circulating antibodies. However, efforts to develop a diverse repertoire of serologically distinct adenovirus vectors may be hindered by the necessity to generate cell lines to allow for the successful propagation of vectors deleted of essential genes. A strategy to construct chimeric adenoviruses whereby the rescue and propagation of an E1 deleted HAdV-B – derived adenoviral vector can be achieved using existing cell lines such as HEK 293 is reported. It is further shown that this strategy may be more widely applicable.
Subject
  • Serology
  • Epidemiology
  • Cell culture
  • Parasitology
  • Adenoviridae
  • Reproduction
  • Senescence
  • Cellular senescence
  • Virus families
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