Research Area Biochemical Engineering, Institute of Chemical Engineering, Vienna University of Technology, Gumpendorferstrasse 1a-166/4, A-1060, Vienna, Austria.
Department of Bioengineering, University of California, San Diego, CA, USA; Novo Nordisk Foundation Center for Biosustainability at the University of California, San Diego School of Medicine, San Diego, CA, USA.
Biotechnol Adv. 2016 Sep-Oct;34(5):621-633. doi: 10.1016/j.biotechadv.2016.02.011. Epub 2016 Mar 3.
The scientific literature concerning Chinese hamster ovary (CHO) cells grows annually due to the importance of CHO cells in industrial bioprocessing of therapeutics. In an effort to start to catalogue the breadth of CHO phenotypes, or phenome, we present the CHO bibliome. This bibliographic compilation covers all published CHO cell studies from 1995 to 2015, and each study is classified by the types of phenotypic and bioprocess data contained therein. Using data from selected studies, we also present a quantitative meta-analysis of bioprocess characteristics across diverse culture conditions, yielding novel insights and addressing the validity of long held assumptions. Specifically, we show that bioprocess titers can be predicted using indicator variables derived from viable cell density, viability, and culture duration. We further identified a positive correlation between the cumulative viable cell density (VCD) and final titer, irrespective of cell line, media, and other bioprocess parameters. In addition, growth rate was negatively correlated with performance attributes, such as VCD and titer. In summary, despite assumptions that technical diversity among studies and opaque publication practices can limit research re-use in this field, we show that the statistical analysis of diverse legacy bioprocess data can provide insight into bioprocessing capabilities of CHO cell lines used in industry. The CHO bibliome can be accessed at http://lewislab.ucsd.edu/cho-bibliome/.
由于中国仓鼠卵巢(CHO)细胞在治疗药物的工业生物加工中的重要性,每年都会有关于 CHO 细胞的科学文献增长。为了开始对 CHO 表型或表型组的广度进行编目,我们提出了 CHO 文献库。该文献汇编涵盖了 1995 年至 2015 年所有已发表的 CHO 细胞研究,并且每个研究都根据其中包含的表型和生物加工数据类型进行分类。使用来自选定研究的数据,我们还对不同培养条件下的生物加工特性进行了定量荟萃分析,得出了新的见解,并解决了长期存在的假设的有效性问题。具体来说,我们表明可以使用来自活细胞密度、活力和培养时间的指示变量来预测生物加工滴度。我们进一步发现,累积活细胞密度(VCD)与最终滴度之间存在正相关,而与细胞系、培养基和其他生物加工参数无关。此外,生长速率与 VCD 和滴度等性能属性呈负相关。总之,尽管有假设认为研究之间的技术多样性和不透明的出版实践可能会限制该领域的研究再利用,但我们表明,对各种传统生物加工数据的统计分析可以深入了解工业中使用的 CHO 细胞系的生物加工能力。CHO 文献库可在 http://lewislab.ucsd.edu/cho-bibliome/ 访问。