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Strategies for Selecting Recombinant CHO Cell Lines for cGMP Manufacturing: Realizing the Potential in Bioreactors

机译:选择重组CHO细胞系用于cGMP制造的策略:实现生物反应器的潜力

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Manufacture of recombinant proteins from mammalian cell lines requires the use of bio-reactor systems at scales of up to 20,000 L. The cost and complexity of such systems can prohibit their extensive use during the process to construct and select the manufacturing cell line. It is therefore common practice to develop a model of the production process in a small scale vessel, such as a shake-flask, where lower costs, ease of handling, and higher throughput are possible. This model can then be used to select a small number of cell lines for further evaluation in bioreactor culture. Here, we extend our previous work investigating cell line construction strategies to assess how well the behavior of cell lines in such a shake-flask assessment predicts behavior in the associated bioreactor production process. A panel of 29 GS-CHO cell lines, all producing the same antibody, were selected to include a mixture of high and low producers from a pool of 175 transfectants. Assessment of this panel in 10 L bioreactor culture revealed wide variation in parameters including growth, productivity, and metabolite utilization. In general, those cell lines which were high producing in the bioreactor cultures had also been higher producing in an earlier shake-flask assessment. However, some changes in rank position of the evaluated cell lines were seen between the two systems. A potential explanation of these observations is discussed and approaches to improve the predictability of assessments used for cell line selection are considered.
机译:从哺乳动物细胞系生产重组蛋白需要使用规模高达20,000 L的生物反应器系统。此类系统的成本和复杂性可能会阻止其在构建和选择生产细胞系的过程中广泛使用。因此,通常的做法是在诸如摇瓶之类的小型容器中开发生产过程的模型,在这种容器中可以实现较低的成本,易于操作和更高的产量。然后可以使用该模型选择少量细胞系,以在生物反应器培养中进行进一步评估。在这里,我们扩展了先前研究细胞系构建策略的工作,以评估这种摇瓶评估中细胞系的行为预测相关生物反应器生产过程中行为的能力。选择一组全部产生相同抗体的29个GS-CHO细胞系,以包括来自175个转染子库的高和低产生者的混合物。在10 L生物反应器培养物中对该板的评估显示出包括生长,生产力和代谢物利用在内的参数差异很大。通常,在较早的摇瓶评估中,在生物反应器培养物中高产的那些细胞系也已经高产。但是,在两个系统之间看到了评估细胞系的秩位置的一些变化。讨论了这些观察结果的潜在解释,并考虑了用于提高细胞系选择评估的可预测性的方法。

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