Kamachi Yasuharu, Omasa Takeshi
Takeda Pharmaceutical Company Limited, 26-1 Muraoka-Higashi 2-chome, Fujisawa, Kanagawa 251-8555, Japan; Graduate School of Advanced Technology and Science, Tokushima University, 2-1 Minamijosanjima-cho, Tokushima 770-8506, Japan.
Faculty of Bioscience and Bioindustry, Tokushima University, 2-1 Minamijosanjima-cho, Tokushima 770-8506, Japan; Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan.
J Biosci Bioeng. 2018 Apr;125(4):470-478. doi: 10.1016/j.jbiosc.2017.11.002. Epub 2017 Dec 8.
Cell culture platform processes are generally employed to shorten the duration of new product development. A fed-batch process with continuous feeding is a conventional platform process for monoclonal antibody production using Chinese hamster ovary (CHO) cells. To establish a simplified platform process, the feeding method can be changed from continuous feed to bolus feed. However, this change induces a rapid increase of osmolality by the bolus addition of nutrients. The increased osmolality suppresses cell culture growth, and the final product concentration is decreased. In this study, osmotic resistant CHO host cells were developed to attain a high product concentration. To establish hyper osmotic resistant CHO host cells, CHO-S host cells were passaged long-term in a hyper osmotic basal medium. There were marked differences in cell growth of the original and established host cells under iso- (328 mOsm/kg) or hyper-osmolality (over 450 mOsm/kg) conditions. Cell growth of the original CHO host cells was markedly decreased by the induction of osmotic stress, whereas cell growth of the hyper osmotic resistant CHO host cells was not affected. The maximum viable cell concentration of hyper osmotic resistant CHO host cells was 132% of CHO-S host cells after the induction of osmotic stress. Moreover, the hyper osmotic resistant characteristic of established CHO host cells was maintained even after seven passages in iso-osmolality basal medium. The use of hyper osmotic resistance CHO host cells to create a monoclonal antibody production cell line might be a new approach to increase final antibody concentrations with a fed-batch process.
细胞培养平台工艺通常用于缩短新产品开发周期。连续补料的分批补料工艺是使用中国仓鼠卵巢(CHO)细胞生产单克隆抗体的传统平台工艺。为建立简化的平台工艺,补料方式可从连续补料改为一次性补料。然而,这种改变会因一次性添加营养物质而导致渗透压迅速升高。渗透压升高会抑制细胞培养生长,降低最终产物浓度。在本研究中,开发了抗渗透压的CHO宿主细胞以获得高产物浓度。为建立抗高渗的CHO宿主细胞,CHO-S宿主细胞在高渗基础培养基中进行长期传代培养。在等渗(328 mOsm/kg)或高渗(超过450 mOsm/kg)条件下,原始宿主细胞和建立的宿主细胞的生长存在显著差异。渗透压应激诱导后,原始CHO宿主细胞的生长明显下降,而抗高渗的CHO宿主细胞的生长不受影响。渗透压应激诱导后,抗高渗的CHO宿主细胞的最大活细胞浓度是CHO-S宿主细胞的132%。此外,即使在等渗基础培养基中传代七次后,建立的CHO宿主细胞的抗高渗特性仍得以维持。使用抗高渗的CHO宿主细胞创建单克隆抗体生产细胞系可能是一种通过分批补料工艺提高最终抗体浓度的新方法。