| Literature DB >> 27997338 |
Arnaud Léon1, Anne-Laure David2, Brice Madeline2, Laurence Guianvarc'h2, Elodie Dureau2, Patrick Champion-Arnaud2, Matthias Hebben2, Thierry Huss3, Benoît Chatrenet4, Klaus Schwamborn2.
Abstract
The selection of a cell substrate is a critical step for the development and manufacturing of a viral vaccine candidate. Several parameters such as cell susceptibility and permissiveness to the viral pathogens but also performance in terms of viral antigens quality and production yields are important considerations when identifying the ideal match between a viral vaccine and cell substrate. The modified vaccinia virus Ankara (MVA) is a replication-deficient viral vector that holds great promise as a vaccine platform, however only limited cell substrates have been tested or are available for industrialization. Here we evaluate the duck embryo-derived EB66® cell line as potential cell substrate for MVA production. To this end, we used two recombinant MVA constructs and demonstrated that EB66® cells are propagating the tested MVA viruses very efficiently, while preserving viral attenuation and transgene expression for up to 20 serial passages. Furthermore we developed upstream and downstream processes that enable industrialization of the virus production. In conclusion, we showed that EB66® cells can be used as potent cell substrate for MVA-based vaccines and represent therefore an attractive alternative for vaccine production.Entities:
Keywords: EB66® cells; Manufacturing process; Modified vaccinia virus Ankara; Vaccine production
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Year: 2016 PMID: 27997338 DOI: 10.1016/j.vaccine.2016.10.043
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641