Kim Byoung Jin, Chang Ho Nam, Oh Duk Jae
Department of Bioscience and Biotechnology, Sejong University, 98 Gunja-dong, Gwangjin-gu, Seoul 143-747, Korea.
Biotechnol Prog. 2007 Sep-Oct;23(5):1186-97. doi: 10.1021/bp0700861. Epub 2007 Aug 11.
Based upon the results of scale-down intermittent perfusion processes, a cell-once-through (COT) perfusion concept was applied to a dual bioreactor system coupled to a Centritech Lab II centrifuge for culture of recombinant Chinese hamster ovary (rCHO) cells for monoclonal antibody production. In this new culture mode, i.e., the COT perfusion process, total spent medium was transferred to the centrifuge and a fixed percentage was removed. Approximately 99% of the viable cells are transferred to another bioreactor filled with fresh medium by single operation of the Centritech Lab II centrifuge system for about 30 min. Accordingly, a significant reduction of the cell-passage frequency to the centrifuge led to minimization of cell damage caused by mechanical shear stress, oxygen limitation, nutrient limitation, and low temperature outside the bioreactor. The effects of culture temperature shift and fortified medium on cell growth and recombinant antibody production in the COT perfusion process were investigated. Although the suppressive effects of low culture temperature on cell growth led to a loss of stability in a long-term COT perfusion culture system, the average antibody concentration at 33 degrees C was 157.8 mg/L, approximately 2.4-fold higher than that at 37 degrees C. By the use of a fortified medium at 37 degrees C, rCHO cells were maintained at high density above 1.2 x 10(7) cells/mL, and antibody was produced continuously in a range of 260-280 mg/L in a stable long-term COT perfusion culture. The proposed new culture mode, the COT perfusion approach, guarantees the recovery of rCHO cells damaged by lowered temperature or high lactate and ammonium concentration. It will be an attractive choice for minimization of cell damage and stable long-term antibody production with high cell density.
基于小规模间歇灌注工艺的结果,将一次性细胞(COT)灌注概念应用于与Centritech Lab II离心机相连的双生物反应器系统,用于培养重组中国仓鼠卵巢(rCHO)细胞以生产单克隆抗体。在这种新的培养模式,即COT灌注工艺中,将全部用过的培养基转移至离心机并去除固定比例的培养基。通过Centritech Lab II离心机系统单次运行约30分钟,约99%的活细胞被转移至另一个装有新鲜培养基的生物反应器中。因此,细胞进入离心机的频率显著降低,使得由机械剪切应力、氧气限制、营养限制以及生物反应器外的低温所导致的细胞损伤降至最低。研究了培养温度变化和强化培养基对COT灌注工艺中细胞生长和重组抗体生产的影响。尽管低培养温度对细胞生长的抑制作用导致长期COT灌注培养系统中出现稳定性丧失的情况,但33℃时的平均抗体浓度为157.8mg/L,约为37℃时的2.4倍。通过在37℃使用强化培养基,rCHO细胞维持在高于1.2×10⁷个细胞/mL的高密度水平,并且在稳定的长期COT灌注培养中,抗体以260 - 280mg/L的范围持续产生。所提出的新培养模式,即COT灌注方法,保证了对因温度降低或高乳酸和铵浓度而受损的rCHO细胞的回收。对于将细胞损伤降至最低以及在高细胞密度下稳定长期生产抗体而言,这将是一个有吸引力的选择。