Perfusion Process Intensification for Lentivirus Production Using a Novel Scale‐Down Model

Process intensification has become an important strategy to lower production costs and increase manufacturing capacities for biopharmaceutical products. In particular for the production of viral vectors like lentiviruses (LVs), the transition from (fed-)batch to perfusion processes is a key strategy to meet the increasing demands for cell and gene therapy applications. However, perfusion processes are associated with higher medium consumption. Therefore, it is necessary to develop appropriate small-scale models to reduce development costs. In this work, we present the use of the acoustic wave separation technology in combination with the Ambr 250 high throughput bioreactor system for intensified perfusion process development using stable LV producer cells. The intensified perfusion process developed in the Ambr 250 model, performed at a harvest rate of 3 vessel volumes per day (VVD) and high cell densities, resulted in a 1.4-fold higher cell-specific functional virus yield and 2.8-fold higher volumetric virus yield compared to the control process at a harvest rate of 1 VVD. The findings were verified at bench scale after optimizing the bioreactor set-up, resulting in a 1.4-fold higher cell-specific functional virus yield and 3.1-fold higher volumetric virus yield.

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Publication Details

Journal
Biotechnology and Bioengineering
Published
2024-11-13
DOI
https://doi.org/10.1002/bit.28880
Citations
7
Primary Topic
Virus-based gene therapy research
Type
article
Field-Weighted Citation Impact
3.85

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article

Perfusion Process Intensification for Lentivirus Production Using a Novel Scale‐Down Model

Maximilian Klimpel, Thomas Noll, Vicky Pirzas, Holger Laux et al.
7 citations
Biotechnology and Bioengineering
Virus-based gene therapy research
3.85
article

Perfusion Process Intensification for Lentivirus Production Using a Novel Scale‐Down Model

Maximilian Klimpel, Thomas Noll, Vicky Pirzas, Holger Laux, Sarah Schwingal, Nikki Indresh Lal, Marta Arrizabalaga Cascallana, Beatrice Pflüger‐Müller
article en
7 citations

Abstract

Process intensification has become an important strategy to lower production costs and increase manufacturing capacities for biopharmaceutical products. In particular for the production of viral vectors like lentiviruses (LVs), the transition from (fed-)batch to perfusion processes is a key strategy to meet the increasing demands for cell and gene therapy applications. However, perfusion processes are associated with higher medium consumption. Therefore, it is necessary to develop appropriate small-scale models to reduce development costs. In this work, we present the use of the acoustic wave separation technology in combination with the Ambr 250 high throughput bioreactor system for intensified perfusion process development using stable LV producer cells. The intensified perfusion process developed in the Ambr 250 model, performed at a harvest rate of 3 vessel volumes per day (VVD) and high cell densities, resulted in a 1.4-fold higher cell-specific functional virus yield and 2.8-fold higher volumetric virus yield compared to the control process at a harvest rate of 1 VVD. The findings were verified at bench scale after optimizing the bioreactor set-up, resulting in a 1.4-fold higher cell-specific functional virus yield and 3.1-fold higher volumetric virus yield.

Biotechnology and BioengineeringVol. 122(2)
Bielefeld University (DE), University College London (GB)
CSL Limited
Openalex Percentile: Top 6%
Virus-based gene therapy research
3.85
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