快速模式细胞系开发(CLD):通过提前悬浮适应和最大限度地延长指数生长阶段的时间,缩短中国仓鼠卵巢 (CHO) 细胞系开发 (CLD) 的时间。

IF 2.5 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Biotechnology Progress Pub Date : 2024-05-08 DOI:10.1002/btpr.3479
Kavya Ganapathy, Cynthia Lam, Joni Tsukuda, Alyssa Sargon, Adrian Nava, Peter Harms, Amy Shen, Gavin Barnard, Shahram Misaghi
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引用次数: 0

摘要

中国仓鼠卵巢(CHO)细胞是表达治疗蛋白的首选系统,大多数生物治疗药物都是由这些细胞系表达的。CHO 表达系统易于扩展,能抵御人类的偶联剂,并具有理想的翻译后修饰,如糖基化。无论如何,药物开发作为一个整体是一个非常昂贵、复杂和耗时的过程。因此,任何能缩短时间的改进都是有价值的,都能让患者更早地获得救命的药物。在此,我们报告了一种在靶向整合(TI)CHO 细胞系开发(CLD)系统中加快细胞系开发(CLD)过程的有效方法(本文称为 SPEED-MODE)。我们的研究结果表明:(1) 尽早对转染池进行单细胞克隆 (SCC);(2) 加快初始滴度筛选的周转时间;(3) 尽早开始培养物的悬浮适应;(4) 尽可能延长 CHO 培养物在指数生长期的时间,可将 CLD 的时间从 ~4 个月缩短到 ~3 个月。有趣的是,假设 CHO 细胞分裂是限制速率的因素,SPEED-MODE 时间与 CHO CLD 的理论最短时间非常吻合。通过 SPEED-MODE CLD 获得的克隆的滴度和产品质量与通过标准 CLD 过程获得的克隆相当。因此,SPEED-MODE CLD 具有在工业环境中生产生物治疗药物的优势,因为它可以在不影响滴度或产品质量的情况下大大缩短 CLD 的时间。
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SPEED-MODE cell line development (CLD): Reducing Chinese hamster ovary (CHO) CLD timelines via earlier suspension adaptation and maximizing time spent in the exponential growth phase

Chinese hamster ovary (CHO) cells are the preferred system for expression of therapeutic proteins and the majority of all biotherapeutics are being expressed by these cell lines. CHO expression systems are readily scalable, resistant to human adventitious agents, and have desirable post-translational modifications, such as glycosylation. Regardless, drug development as a whole is a very costly, complicated, and time-consuming process. Therefore, any improvements that result in reducing timelines are valuable and can provide patients with life-saving drugs earlier. Here we report an effective method (termed SPEED-MODE, herein) to speed up the Cell line Development (CLD) process in a targeted integration (TI) CHO CLD system. Our findings show that (1) earlier single cell cloning (SCC) of transfection pools, (2) speeding up initial titer screening turnaround time, (3) starting suspension adaptation of cultures sooner, and (4) maximizing the time CHO cultures spend in the exponential growth phase can reduce CLD timelines from ~4 to ~3 months. Interestingly, SPEED-MODE timelines closely match the theoretical minimum timeline for CHO CLD assuming that CHO cell division is the rate limiting factor. Clones obtained from SPEED-MODE CLD yielded comparable titer and product quality to those obtained via a standard CLD process. Hence, SPEED-MODE CLD is advantageous for manufacturing biotherapeutics in an industrial setting as it can significantly reduce CLD timelines without compromising titer or product quality.

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来源期刊
Biotechnology Progress
Biotechnology Progress 工程技术-生物工程与应用微生物
CiteScore
6.50
自引率
3.40%
发文量
83
审稿时长
4 months
期刊介绍: Biotechnology Progress , an official, bimonthly publication of the American Institute of Chemical Engineers and its technological community, the Society for Biological Engineering, features peer-reviewed research articles, reviews, and descriptions of emerging techniques for the development and design of new processes, products, and devices for the biotechnology, biopharmaceutical and bioprocess industries. Widespread interest includes application of biological and engineering principles in fields such as applied cellular physiology and metabolic engineering, biocatalysis and bioreactor design, bioseparations and downstream processing, cell culture and tissue engineering, biosensors and process control, bioinformatics and systems biology, biomaterials and artificial organs, stem cell biology and genetics, and plant biology and food science. Manuscripts concerning the design of related processes, products, or devices are also encouraged. Four types of manuscripts are printed in the Journal: Research Papers, Topical or Review Papers, Letters to the Editor, and R & D Notes.
期刊最新文献
Non-thermal plasma decontamination of microbes: a state of the art. Mechanistic model of minute virus of mice elution behavior in anion exchange chromatography purification. Comparing in silico flowsheet optimization strategies in biopharmaceutical downstream processes. General strategies for IgG-like bispecific antibody purification. Issue Information
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