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This article is part of the supplement: 22nd European Society for Animal Cell Technology (ESACT) Meeting on Cell Based Technologies

Open Access Meeting abstract

Medium and feed optimization for fed-batch production of a monoclonal antibody in CHO cells

Nadine Kochanowski*, Gaetan Siriez, Sarah Roosens and Laetitia Malphettes

Author affiliations

Cell Culture Process Development Group, Biological Process Development, UCB Pharma S.A., Braine L’Alleud, 1420, Belgium

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Citation and License

BMC Proceedings 2011, 5(Suppl 8):P75  doi:10.1186/1753-6561-5-S8-P75


The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1753-6561/5/S8/P75


Published:22 November 2011

© 2011 Kochanowski et al; licensee BioMed Central Ltd.

This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Background

Mammalian cells are used extensively in the production of recombinant proteins, and of monoclonal antibodies (MAbs) in particular. The trend towards avoiding animal-derived components in biopharmaceutical production processes has led to the extensive use of non-animal origin hydrolysates such as plant hydrolysates or yeast hydrolysates. The source of hydrolysates affects cell growth and productivity and may also affect product quality. Accordingly, careful consideration should be given during process and cell culture media development, in order to determine the appropriate type and amount of hydrolysates to be added, for the cell and product at hand.

In this study, we assessed the impact of several hydrolysate additives and chemically defined (CD) commercial feeds on MAb titers, MAb average specific productivity (average Qp), cell viabilities and metabolite profiles in suspension cultures of recombinant CHO cells expressing a monoclonal antibody in shake flasks and 2 L bioreactors.

Materials and methods

Initial experiments were performed using chemically defined culture medium in 125 mL shake flasks with 50 mL working volume. CHO cells were seeded at 0.3x106 viable cells/mL and incubated at 140 rpm, 36.5°C and 5% CO2. 2L stirred tank bioreactors (Sartorius) were carried out for 14 days in a fed-batch mode in a chemically defined medium supplemented with chemically defined feeds and hydrolysates. Glucose was maintained between 1 and 6 g/L. At the day of harvest the clarification was performed by depth filtration. Analysis of daily samples included determinations of cell viability, cell density, metabolites, osmolality and product titer. Product concentration of the supernatant samples was quantified using Octet QK and Protein A high performance liquid chromatography (HPLC). Protein characterization of Protein-A purified samples were profiled by reduced and non reduced SDS PAGE. Isoelectric focusing (IEF) analysis of Protein-A purified MAb was carried out using a iCE280 IEF Analyzer. Aggregates and monomers proportion were determined by using size exclusion chromatography. Acidic and basic species were characterized using anion exchange (AEX) HPLC. Oligosaccharides were cleaved enzymatically using N-Glycanase, then labeled with 2-aminobenzamide and analyzed by HPLC using an amide column and a fluorescent detector.

Results

Several chemically defined feeds and hydrolysates were assessed on CHO cells expressing a monoclonal antibody in fed-batch mode. The performance of the developed process was compared to an existing in-house platform process.

Nine different chemically defined feeds were assessed and added at different concentrations (Table 1). Among the feeds tested, addition of CD Feed 8 and 9 brought a 150 % improvement on MAb titer on the day of harvest compared to the platform process. All the MAb titers measured were ranging from 2 g/L to 6 g/L (Figure 1).

Table 1. Chemically defined feeds and hydrolysates tested

thumbnailFigure 1. Relative percentage of improvement on MAb titer. Note: Platform process in shake flask was used as the 100% reference for all the calculations of relative percentage of improvement on Mab titer measured the day of harvest

Six different hydrolysates were assessed at different concentrations in fed-batch mode (Table 1). Among the feeds tested, addition of hydrolysate 1 and hydrolysate 2 showed an improvement of 175% and 167% respectively on MAb yield.

To identify potential synergies between hydrolysates, the best hydrolysates from previous experiments were selected and were tested in combination at different ratios on CHO cell cultures (Table 1). Antibody concentration at harvest was 290% higher with some of the hydrolysate combinations.

Based on feed combination optimization results, the number of bolus feeds and the feed addition timing were then fine-tuned using the best hydrolysate combination. Reducing the number of bolus feeds enabled to reduce ammonia and osmolality while maintaining a high MAb titer (Figure 1). Moreover, under these conditions, cell viabilities were maintained above 80% throughout the culture (data not shown).

Based on experimental results obtained in shake flasks, the best hydrolysate combination (3 feeds and 4 feeds) and CD feed were assessed on CHO cells cultured in 2 L stirred tank bioreactors. Cell growth and cell metabolism were monitored daily throughout the cultures in bioreactors. By feeding the cultures with hydrolysates, addition of 3 or 4 bolus feeds enabled to attain similar maximum viable cell count. Addition of chemically defined feed led to a 30% higher maximum viable cell count. Cell viabilities were maintained at acceptable values throughout the cultures in the established culture conditions. Lactate profiles were similar independently of the feeding regime. Decreasing the number of hydrolysate feeds enabled to maintain osmolality and ammonia at acceptable concentrations for CHO cell growth and product quality. Cell growth performance and metabolism profiles observed in 2 L bioreactors were comparable to those observed in shake flasks.

Product titers have been measured throughout the fed-batch cultures with the Octet QK system. The MAb titers were in a 2-6 g/L range for all the tested feeding regimes at the day of harvest. A combination of hydrolysates and a chemically defined feed supplementation showed an improvement of 296% and 245% on MAb concentration at the day of harvest in comparison to the platform process (Figure 1). MAb average specific productivity (Qp) was increased by 700% and 360% by adding 4 feeds of hydrolysates and chemically defined feed respectively. Decreasing the number of hydrolysate feeds showed a slight decrease on MAb titer and on Qp.

Product quality attributes were determined on cell culture clarified fluids after Protein-A purification. Reduced and non reduced SDS electrophoresis, isoelectric focusing (IEF) analysis, gel permeation HPLC, size exclusion (SEC) chromatography, anion exchange HPLC (AEX) have been used to characterize the Protein-A purified MAb. Product quality data was comparable for all the feeding regimes tested in 2 L bioreactors.

Conclusions

Hydrolysate combination additions significantly improved MAb production in comparison to single hydrolysate addition or chemically defined feeds. Number of bolus feeds and feeding timing optimization enabled us to improve the process robustness taking into account the impact of feeding strategy on cell metabolism and product quality. The feeding regimes established in shake flasks led to similar culture performance in 2 L bioreactors.

Acknowledgments

We wish to acknowledge BD Biosciences, Sheffield, Life Tech and Thermofisher for providing media and feeds. We also wish to acknowledge Mari Spitali, Natasha Hinkel, Vanessa Auquier and Marc Speleers for Protein-A purification and product quality analysis.