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7271269 
Journal Article 
Development of a Manufacturing Process for the Production of a Canine Adenovirus Type 2 (CAV-2) Vector Using MDCK Cells 
Fernandes, P; Santiago, V; Viana, N; Kremer, EJ; Coroadinha, AnaS; Alves, PM; , 
2012 
SPRINGER 
DORDRECHT 
671-674 
WOS:000398249100106 
Adenovirus vectors are one of the most efficient vehicles for delivering nucleic acids into mammalian cells. However, human adenoviruses are ubiquitous in all population, posing memory immunity responses obstacles for their use during clinical gene transfer. To circumvent this drawback, nonhuman adenovirus vectors like CAV-2 are being developed. It was demonstrated that HD CAV-2 vectors have numerous advantages for clinical gene transfer leading to long-term expression in vivo gene transfer in the rodent CNS. Since the final goal of this work is the establishment of a complete manufacturing process for first generation (Delta E1) and helper dependent (HD) CAV-2 vectors, allowing the reduction of production costs and higher safety, first it is necessary the development of a robust producer cell line that enables high production in serum-free media. In order to evaluate the cell growth and Delta E1 CAV-2 vectors production, MDCK El, a cell line based on Madin-Darby Canine Kidney (MDCK), a cell line commonly used for the production of biopharmaceuticals and vaccines, was adapted to two commercial serum-free media: Ex-cell and Optipro. When comparing with serum supplemented medium, Optipro medium allows almost 4 times higher cell densities while maintaining the vector production yields. These results show Optipro as the best serum-free medium for the growth and production of CAV-2 vectors. 
Jenkins, N; Barron, N; Alves, PM; 
978-94-007-0883-9 
21st Annual Meeting of the European-Society-for-Animal-Cell-Technology (ESACT) 
Dublin, IRELAND