Preventing spontaneous genetic rearrangements in the transgene cassettes of adenovirus vectors.

Biotechnol Bioeng 2012 Mar 6;109(3):719-28. Epub 2011 Nov 6.

The Jenner Institute, University of Oxford, Roosevelt Drive, Oxford OX3 7DQ, UK.

First-generation, E1/E3-deleted adenoviral vectors with diverse transgenes are produced routinely in laboratories worldwide for development of novel prophylactics and therapies for a variety of applications, including candidate vaccines against important infectious diseases, such as HIV/AIDS, tuberculosis, and malaria. Here, we show, for two different transgenes (both encoding malarial antigens) inserted at the E1 locus, that rare viruses containing a transgene-inactivating mutation exhibit a selective growth advantage during propagation in E1-complementing HEK293 cells, such that they rapidly become the major or sole species in the viral population. For one of these transgenes, we demonstrate that viral yield and cytopathic effect are enhanced by repression of transgene expression in the producer cell line, using the tetracycline repressor system. In addition to these transgene-inactivating mutations, one of which occurred during propagation of the pre-viral genomic clone in bacteria, and the other after viral reconstitution in HEK293 cells, we describe two other types of mutation, a small deletion and a gross rearranging duplication, in one of the transgenes studied. These were of uncertain origin, and the effects on transgene expression and viral growth were not fully characterized. We demonstrate that, together with minor protocol modifications, repression of transgene expression in HEK293 cells during viral propagation enables production of a genetically stable chimpanzee adenovirus vector expressing a malarial antigen which had previously been impossible to derive. These results have important implications for basic and pre-clinical studies using adenoviral vectors and for derivation of adenoviral vector products destined for large-scale amplification during biomanufacture.

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http://dx.doi.org/10.1002/bit.24342DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981243PMC
March 2012
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References

(Supplied by CrossRef)
Efficient generation of recombinant adenovirus vectors by homologous recombination in Escherichia coli
Chartier et al.
J Virol 1996

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