Perfusion

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High cell density perfusion of antibody producing CHO cells in disposable WAVE Bioreactor™ using ATF or TFF

Collaboration: GE Healthcare, Sweden - USA


High cell density perfusion process of monoclonal antibody producing CHO cells was developed in Wave ATF TFFdisposable WAVE Bioreactor™ using tangential flow filtration by external hollow fiber filter (0.2 um microfilter) as cell separation device. Either ‘classical’ Tangential Flow Filtration (TFF) or Alternating Tangential Flow system (ATF) equipment were used and compared for their process performances. 


Consistency and reproducibility of both TFF and ATF perfusion cultures were shown at 20 to 35 * 1E6 cells/mL cell density stabilized by cell bleeds. In order to minimize the nutrients deprivation and metabolites accumulation, a perfusion rate strictly correlated to the cell density was chosen: a Cell Specific Perfusion Rate (CSPR) controlled-feed strategy of 0.05 nL/cell/day was identified and applied onwards in this study to achieve higher cell densities. In this study, this strategy allowed maintaining the cells in growing state and at high viability as shown when the cell density was then stably maintained at 1 to 1.2 * 1E8 cells/mL by cell bleeds. Finally, with the settings used here, maximal cell densities of 2.14 * 1E8 cells/mL and 1.32 * 1E8 cells/mL were reached using TFF and ATF systems respectively. To our knowledge, it is the first time that a density of CHO cells larger than 2 * 1E8 cells/mL was achieved in a wave-agitated bioreactor. 


The present perfusion process setting was then mounted with ultrafilter cartridges (UF) to evaluate the performances of this system. Cell densities up to 1E8 were obtained using UF TFF or UF ATF. Using ATF or TFF in perfusions by microfiltration (MF) or ultrafiltration, the cells produced comparable amounts of IgG. The IgG was partially retained by the MF cartridge using ATF or TFF but the retention was higher in the TFF system. The consequence of this retention was mainly an IgG loss when cell broth from the bioreactor was discarded in the daily bleeds while maintaining the cell density at a given level. The MF TFF was thus less favorable for the production of IgG in comparison with MF ATF. The production obtained by perfusion process was compared to fed-batch process. About 5.2 times more IgG could be harvested using perfusion by ATF or TFF, MF or UF, instead of fed-batch after 12 days of culture.


Furthermore, cell cryopreservations at 0.5 * 1E8 cells/mL and 1E8 cells/mL were performed using cells directly taken from perfusion at 1E8 cells/mL cell density. Cell thaw and expansion showed excellent cell resuscitation and expected IgG production for this cell line, leading to the conclusion that this system could be a reliable process for generation of cell banks.


 

Marie-Françoise Clincke, Carin Mölleryd, Ye Zhang, Eva Lindskog, Kieron Walsh, Véronique Chotteau. Very high density of CHO cells in perfusion by ATF or TFF in WAVE bioreactor™- Part I. effect of the cell density on the process. Biotechnology Progress 2013


Marie-Françoise Clincke, Carin Mölleryd, Puneeth K Samani, Eva Lindskog, Eric Fäldt, Kieron Walsh, Véronique Chotteau. Very high density of CHO cells in perfusionby ATF or TFF in WAVE bioreactor™ – Part II: Applications for antibody production and cryopreservation. Biotechnology Progress 2013




Perfusion of IgG producing Chinese Hamster Ovary cells in a novel single-use bioreactor, CellTank, integrating the cell separation device   

Collaboration: Belach (Sweden), CerCell (Danmark) 


Figures CelltankA perfusion integrated Single-use bioreactor (SUB) culture system CellTank was developed for highly efficient production of recombinant products from mammalian cell cultures. The SUB contained a matrix (CellCore) integrated in the CellTank and harbouring the cells. A real-time biomass sensor using the dielectric properties of living cells (bioimpedance) was installed to measure the live cell density. In this study, recombinant Chinese Hamster Ovary cells producing IgG monoclonal antibody were cultivated in a CellTank 2202 prototype. The operations and performance were studied in long-term perfusion cultivation.


A maximal high cell density measured as 200 pF/cm was
achieved after 13 days of exponential growth (1 pF/cm is equivalent to 106 cells/mL). In a second run, a high cell density of 130 pF/cm was maintained for 11 days with temperature lowered gradually from 37°C to 29°C. The IgG cell specific productivity was comparable or higher than the one measured in batch culture in Erlenmeyer flasks. There was no retention of IgG in the CellCore matrix.


As a bench-top single-use bioreactor with integrated cell separation device, CellTank showed to sustain high cell density above 100 x  106 viable cells/mL without IgG retention in the matrix. As a perfusion system, CellTank was easy and handy to operate.