Spens Erika, Häggström Lena
School of Biotechnology, Department of Bioprocess Technology, Royal Institute of Technology, AlbaNova University Center, SE-106 91 Stockholm, Sweden.
Biotechnol Bioeng. 2007 Dec 15;98(6):1183-94. doi: 10.1002/bit.21509.
A chemically defined protein and animal component-free fed-batch process for an NS0 cell line producing a human IgG(1) antibody has been developed. The fed-batch feed profile was optimised in a step-wise manner. Depletion of measurable compounds was determined by direct analysis. The cellular need for non-measurable compounds was tested by continued culturing of cell suspension, removed from the bioreactor, in shake-flasks supplemented with critical substances. In the final fed-batch culture, 8.4 x 10(6) viable cells mL(-1) and 625 mg antibody L(-1) was obtained as compared to 2.3 x 10(6) cells mL(-1) and 70 mg antibody L(-1) in batch. The increase in cell density, in combination with a prolonged declining phase where antibody formation continued, resulted in a 6.2-fold increase in total cell yield, a 10.5-fold increase in viable cell hours and an 11.4-fold increase in product yield. These improvements were obtained by using a feed with glucose, glutamine, amino acids, lipids, sodium selenite, ethanolamine and vitamins. Specifically, supplementation with lipids (cholesterol) had a drastic effect on the maximum viable cell density. Calcium, magnesium and potassium were not depleted and a feed also containing iron, lithium, manganese, phosphorous and zinc did not significantly enhance the cell yield. The growth and death profiles in the final fed-batch indicated that nutrient deprivation was not the main cause of cell death. The ammonium concentration and the osmolality increased to potentially inhibitory levels, but an imbalance in the supply of growth/survival factors may also contribute to termination of the culture.
已开发出一种用于生产人IgG(1)抗体的NS0细胞系的化学成分确定且无动物成分的补料分批培养工艺。补料分批培养的补料曲线以逐步方式进行了优化。可测量化合物的消耗通过直接分析来确定。细胞对不可测量化合物的需求通过从生物反应器中取出的细胞悬液在补充关键物质的摇瓶中继续培养来测试。在最终的补料分批培养中,获得了8.4×10(6)个活细胞/mL和625mg抗体/L,而分批培养中为2.3×10(6)个细胞/mL和70mg抗体/L。细胞密度的增加,加上抗体形成持续的延长衰退期,导致总细胞产量增加6.2倍,活细胞小时数增加10.5倍,产物产量增加11.4倍。这些改进是通过使用含有葡萄糖、谷氨酰胺、氨基酸、脂质、亚硒酸钠、乙醇胺和维生素的补料实现的。具体而言,补充脂质(胆固醇)对最大活细胞密度有显著影响。钙、镁和钾未被耗尽,并且含有铁、锂、锰、磷和锌的补料也未显著提高细胞产量。最终补料分批培养中的生长和死亡曲线表明,营养剥夺不是细胞死亡的主要原因。铵浓度和渗透压增加到潜在抑制水平,但生长/存活因子供应的不平衡也可能导致培养终止。