Cell-culture process optimization via model-based predictions of metabolism and protein glycosylation

被引:16
作者
Reddy, Jayanth Venkatarama [1 ]
Raudenbush, Katherine [1 ]
Papoutsakis, Eleftherios Terry [1 ,2 ]
Ierapetritou, Marianthi [1 ]
机构
[1] Univ Delaware, Dept Chem & Biomol Engn, Newark, DE 19716 USA
[2] Univ Delaware, Delaware Biotechnol Inst, Dept Biol Sci, Newark, DE USA
关键词
Kinetic modeling; Metabolic flux analysis; Flux balance analysis; N -linked glycosylation model; Bioreactor optimization; Biomanufacturing process intensification; Mechanistic modeling; Parameter estimation; N-LINKED GLYCOSYLATION; SUSPENDED ANIMAL-CELLS; HAMSTER OVARY CELLS; LOW-OXYGEN TENSION; FED-BATCH CULTURE; HUMAN T-CELLS; MONOCLONAL-ANTIBODY; FLUX ANALYSIS; CHO-CELLS; MATHEMATICAL-MODEL;
D O I
10.1016/j.biotechadv.2023.108179
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In order to meet the rising demand for biologics and become competitive on the developing biosimilar market, there is a need for process intensification of biomanufacturing processes. Process development of biologics has historically relied on extensive experimentation to develop and optimize biopharmaceutical manufacturing. Experimentation to optimize media formulations, feeding schedules, bioreactor operations and bioreactor scale up is expensive, labor intensive and time consuming. Mathematical modeling frameworks have the potential to enable process intensification while reducing the experimental burden. This review focuses on mathematical modeling of cellular metabolism and N-linked glycosylation as applied to upstream manufacturing of biologics. We review developments in the field of modeling cellular metabolism of mammalian cells using kinetic and stoichiometric modeling frameworks along with their applications to simulate, optimize and improve mechanistic understanding of the process. Interest in modeling N-linked glycosylation has led to the creation of various types of parametric and non-parametric models. Most published studies on mammalian cell metabolism have performed experiments in shake flasks where the pH and dissolved oxygen cannot be controlled. Efforts to understand and model the effect of bioreactor-specific parameters such as pH, dissolved oxygen, temperature, and bioreactor heterogeneity are critically reviewed. Most modeling efforts have focused on the Chinese Hamster Ovary (CHO) cells, which are most commonly used to produce monoclonal antibodies (mAbs). However, these modeling approaches can be generalized and applied to any mammalian cell-based manufacturing platform. Current and potential future applications of these models for Vero cell-based vaccine manufacturing, CAR-T cell therapies, and viral vector manufacturing are also discussed. We offer specific recommendations for improving the applicability of these models to industrially relevant processes.
引用
收藏
页数:31
相关论文
共 263 条
[1]   Variable selection and parameter estimation of viral amplification in vero cell cultures dedicated to the production of a dengue vaccine [J].
Abbate, Thomas ;
Dewasme, Laurent ;
Vande Wouwer, Alain .
BIOTECHNOLOGY PROGRESS, 2019, 35 (01)
[2]   Increasing batch-to-batch reproducibility of CHO-cell cultures using a model predictive control approach [J].
Aehle, Mathias ;
Bork, Kaya ;
Schaepe, Sebastian ;
Kuprijanov, Artur ;
Horstkorte, Ruediger ;
Simutis, Rimvydas ;
Luebbert, Andreas .
CYTOTECHNOLOGY, 2012, 64 (06) :623-634
[3]   A semi-empirical glycosylation model of a camelid monoclonal antibody under hypothermia cell culture conditions [J].
Aghamohseni, Hengameh ;
Spearman, Maureen ;
Ohadi, Kaveh ;
Braasch, Katrin ;
Moo-Young, Murray ;
Butler, Michael ;
Budman, Hector M. .
JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY, 2017, 44 (07) :1005-1020
[4]   Effects of nutrient levels and average culture pH on the glycosylation pattern of camelid-humanized monoclonal antibody [J].
Aghamohseni, Hengameh ;
Ohadi, Kaveh ;
Spearman, Maureen ;
Krahn, Natalie ;
Moo-Young, Murray ;
Scharer, Jeno M. ;
Butler, Mike ;
Budman, Hector M. .
JOURNAL OF BIOTECHNOLOGY, 2014, 186 :98-109
[5]   Effect of Culture Temperature on Erythropoietin Production and Glycosylation in a Perfusion Culture of Recombinant CHO Cells [J].
Ahn, Woo Suk ;
Jeon, Jae-Jin ;
Jeong, Yeong-Ran ;
Lee, Seung Joo ;
Yoon, Sung Kwan .
BIOTECHNOLOGY AND BIOENGINEERING, 2008, 101 (06) :1234-1244
[6]   Parallel labeling experiments with [1,2-13C]glucose and [U-13C]glutamine provide new insights into CHO cell metabolism [J].
Ahn, Woo Suk ;
Antoniewicz, Maciek R. .
METABOLIC ENGINEERING, 2013, 15 :34-47
[7]   Towards dynamic metabolic flux analysis in CHO cell cultures [J].
Ahn, Woo Suk ;
Antoniewicz, Maciek R. .
BIOTECHNOLOGY JOURNAL, 2012, 7 (01) :61-74
[8]   Population balance modelling captures host cell protein dynamics in CHO cell cultures [J].
Alhuthali, Sakhr ;
Kontoravdi, Cleo .
PLOS ONE, 2022, 17 (03)
[9]   Scale-down cultivation in mammalian cell bioreactors-The effect of bioreactor mixing time on the response of CHO cells to dissolved oxygen gradients [J].
Anane, Emmanuel ;
Knudsen, Ida Molgaard ;
Wilson, Giles C. .
BIOCHEMICAL ENGINEERING JOURNAL, 2021, 166
[10]   THE EFFECT OF AMMONIA ON THE O-LINKED GLYCOSYLATION OF GRANULOCYTE-COLONY-STIMULATING FACTOR PRODUCED BY CHINESE-HAMSTER OVARY CELLS [J].
ANDERSEN, DC ;
GOOCHEE, CF .
BIOTECHNOLOGY AND BIOENGINEERING, 1995, 47 (01) :96-105