| Literature DB >> 34209694 |
Anna Offersgaard1,2, Carlos Rene Duarte Hernandez1,2, Anne Finne Pihl1,2, Rui Costa1,2, Nandini Prabhakar Venkatesan3, Xiangliang Lin3, Long Van Pham1,2, Shan Feng1,2, Ulrik Fahnøe1,2, Troels Kasper Høyer Scheel1,2, Santseharay Ramirez1,2, Udo Reichl4, Jens Bukh1,2, Yvonne Genzel4, Judith Margarete Gottwein1,2.
Abstract
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has demonstrated the value of pursuing different vaccine strategies. Vaccines based on whole viruses, a widely used vaccine technology, depend on efficient virus production. This study aimed to establish SARS-CoV-2 production in the scalable packed-bed CelCradleTM 500-AP bioreactor. CelCradleTM 500-AP bottles with 0.5 L working volume and 5.5 g BioNOC™ II carriers were seeded with 1.5 × 108 Vero (WHO) cells, approved for vaccine production, in animal component-free medium and infected at a multiplicity of infection of 0.006 at a total cell number of 2.2-2.5 × 109 cells/bottle seven days post cell seeding. Among several tested conditions, two harvests per day and a virus production temperature of 33 °C resulted in the highest virus yield with a peak SARS-CoV-2 infectivity titer of 7.3 log10 50% tissue culture infectious dose (TCID50)/mL at 72 h post-infection. Six harvests had titers of ≥6.5 log10 TCID50/mL, and a total of 10.5 log10 TCID50 were produced in ~5 L. While trypsin was reported to enhance virus spread in cell culture, addition of 0.5% recombinant trypsin after infection did not improve virus yields. Overall, we demonstrated successful animal component-free production of SARS-CoV-2 in well-characterized Vero (WHO) cells in a scalable packed-bed bioreactor.Entities:
Keywords: COVID-19; CelCradle; Vero cells; animal component-free; inactivated vaccine; packed-bed; scalable bioreactor; severe acute respiratory syndrome coronavirus 2; whole virus vaccine
Year: 2021 PMID: 34209694 DOI: 10.3390/vaccines9070706
Source DB: PubMed Journal: Vaccines (Basel) ISSN: 2076-393X