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More than half a million people die every year from complications of seasonal influenza, and vaccination stands as the most effective method to prevent and limit outbreaks of the disease. Cell culture processes offer a more flexible and responsive alternative for the current egg-based vaccine production systems. Intensification of cell-based vaccine manufacturing focus on the development of high cell density processes and perfusion-based strategies. Here, a high-innoculum fed-batch (HIFB) process with continuous virus harvest will be applied for pandemic influenza vaccine production in suspension MDCK cells, as to maximize virus production while minimizing media handling. For this, a set of small-scale experiments will be executed to assess the metabolic demands. Two bioreactor runs, using a single-use bioreactor coupled to a scalable single-use hollow-fiber membrane as cell retention device, will be performed to demostrate the scalability of the system.
Olivier Henry
Max Planck Institute for Dynamics of Complex Technical Systems
Engineering
Biotechnology
Polytechnique Montréal
Globalink Research Award
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