School of Pharmacy, Wuhan University, East Lake Road 185, Wuchang District, Wuhan, 430071, Hubei Province, China.
Shanghai Taiyin Biotech Co., Ltd., Shanghai, 201203, China.
Appl Microbiol Biotechnol. 2019 Feb;103(3):1217-1229. doi: 10.1007/s00253-018-9555-7. Epub 2018 Dec 15.
Hyperosmolality has been commonly investigated due to its effects on the production and quality characteristics of monoclonal antibodies (mAbs) produced in CHO cell fed-batch cultures. However, the application of hyperosmolality at different times and its effect on biopotency have seldom been researched, especially in perfusion culture. In our study, different degrees of hyperosmolality induced by sodium chloride were investigated in anti-IgE rCHO cell fed-batch cultures and anti-CD52 rCHO cell perfusion cultures during the initial and stable phases. The results showed that the initial hyperosmolality group (IHG) in fed-batch and early phase of perfusion cultures exhibited significant suppression of the viable cell density yet an enhancement in specific productivity, whereas the stable hyperosmolality group (SHG) achieved higher mAb production in both fed-batch and perfusion cultures. Additionally, the SHG produced less aggregates and acidic charge variants than IHG in fed-batch culture, which differed from perfusion cultures. However, the contents of non-glycosylation heavy chain (NGHC) and man5 were higher in SHG than in IHG in fed-batch cultures at plus 60 and 120 mOsm/kg, which was similar to perfusion cultures. Furthermore, the biopotency in the IHG was higher than in the SHG at plus 60 and 120 mOsm/kg in fed-batch cultures, which is similar to complement-dependent cytotoxicity (CDC) efficacy in perfusion cultures. The biopotency of all group was acceptable, except FI3. Thus, the study shows that hyperosmolality at a certain level could be beneficial for both mAb production, quality and biopotency, which could play an important role in process development for commercial production.
由于高渗透压对 CHO 细胞分批补料培养中产生的单克隆抗体(mAb)的产量和质量特性的影响,高渗透压一直受到广泛研究。然而,在不同时间施加高渗透压及其对生物效价的影响很少被研究,特别是在灌注培养中。在本研究中,考察了氯化钠诱导的不同程度的高渗透压在抗 IgE rCHO 细胞分批补料培养和抗 CD52 rCHO 细胞灌注培养初始和稳定阶段的作用。结果表明,在分批补料和灌注培养的初始阶段,高渗透压初始组(IHG)显著抑制活细胞密度,但提高了比生产率,而高渗透压稳定组(SHG)在分批补料和灌注培养中均实现了更高的 mAb 产量。此外,与灌注培养相比,在分批补料培养中,SHG 产生的聚集物和酸性电荷变异体比 IHG 少,但在分批补料培养中,SHG 的非糖基化重链(NGHC)和 man5 含量高于 IHG,这与灌注培养相同。此外,在分批补料培养中,在+60 和+120 mOsm/kg 时,SHG 的生物效价高于 IHG,这与灌注培养中的补体依赖性细胞毒性(CDC)效力相似。除 FI3 外,所有组的生物效价均可以接受。因此,该研究表明,在一定水平的高渗透压对 mAb 生产、质量和生物效价都有益,这可能在商业生产的工艺开发中发挥重要作用。