Chung Wai Keen, Russell Brian, Yang Yanhong, Handlogten Michael, Hudak Suzanne, Cao Mingyan, Wang Jihong, Robbins David, Ahuja Sanjeev, Zhu Min
Purification Process Sciences, MedImmune LLC, One MedImmune Way, Gaithersburg, Maryland.
Cell Culture and Fermentation Sciences, MedImmune LLC, One MedImmune Way, Gaithersburg, Maryland.
Biotechnol Bioeng. 2017 Jun;114(6):1264-1274. doi: 10.1002/bit.26265. Epub 2017 Mar 6.
Antibody disulfide bond reduction during monoclonal antibody (mAb) production is a phenomenon that has been attributed to the reducing enzymes from CHO cells acting on the mAb during the harvest process. However, the impact of antibody reduction on the downstream purification process has not been studied. During the production of an IgG mAb, antibody reduction was observed in the harvested cell culture fluid (HCCF), resulting in high fragment levels. In addition, aggregate levels increased during the low pH treatment step in the purification process. A correlation between the level of free thiol in the HCCF (as a result of antibody reduction) and aggregation during the low pH step was established, wherein higher levels of free thiol in the starting sample resulted in increased levels of aggregates during low pH treatment. The elevated levels of free thiol were not reduced over the course of purification, resulting in carry-over of high free thiol content into the formulated drug substance. When the drug substance with high free thiols was monitored for product degradation at room temperature and 2-8°C, faster rates of aggregation were observed compared to the drug substance generated from HCCF that was purified immediately after harvest. Further, when antibody reduction mitigations (e.g., chilling, aeration, and addition of cystine) were applied, HCCF could be held for an extended period of time while providing the same product quality/stability as material that had been purified immediately after harvest. Biotechnol. Bioeng. 2017;114: 1264-1274. © 2017 The Authors. Biotechnology and Bioengineering Published by Wiley Periodicals Inc.
在单克隆抗体(mAb)生产过程中,抗体二硫键还原是一种已被归因于收获过程中CHO细胞的还原酶作用于mAb的现象。然而,抗体还原对下游纯化过程的影响尚未得到研究。在生产一种IgG单克隆抗体时,在收获的细胞培养液(HCCF)中观察到抗体还原,导致片段水平升高。此外,在纯化过程的低pH处理步骤中聚集体水平增加。建立了HCCF中游离巯基水平(由于抗体还原)与低pH步骤中聚集之间的相关性,其中起始样品中较高水平的游离巯基导致低pH处理期间聚集体水平增加。游离巯基水平在纯化过程中并未降低,导致高游离巯基含量带入最终药物制剂中。当监测含有高游离巯基的药物制剂在室温及2-8°C下的产品降解情况时,与收获后立即纯化的HCCF产生的药物制剂相比,观察到更快的聚集速率。此外,当采用抗体还原缓解措施(如冷却、通气和添加胱氨酸)时,HCCF可以保存更长时间,同时提供与收获后立即纯化的材料相同的产品质量/稳定性。《生物技术与生物工程》2017年;114: 1264-1274。© 2017作者。《生物技术与生物工程》由威利期刊公司出版