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Accelerating and de-risking CMC development with transposon-derived manufacturing cell lines

机译:通过转座子衍生的制造细胞系加速和破坏CMC开发

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The development of highly productive, genetically stable manufacturing cell lines is on the critical path to IND filing for protein-based biologic drugs. Here, we describe the Leap-In Transposase (R) platform, a novel transposon-based mammalian (e.g., Chinese hamster ovary) cell line development system that produces high-titer stable pools with productivity and product quality attributes that are highly comparable to clones that are subsequently derived therefrom. The productivity distributions of clones are strongly biased toward high producers, and genetic and expression stability is consistently high. By avoiding the poor integration rates, concatemer formation, detrimental transgene recombination, low average expression level, unpredictable product quality, and inconsistent genetic stability characteristic of nonhomologous recombination methods, Leap-In provides several opportunities to de-risk programs early and reduce timelines and resources.
机译:高效的发展,基因稳定的制造细胞系是临床归档的基于蛋白质的生物药物的关键路径。 在这里,我们描述了一种跨越转座酶(R)平台,一种新型的转座子哺乳动物(例如,中国仓鼠卵巢)细胞系发育系统,产生高滴度稳定池,其生产力和产品质量属性与克隆具有高度可比性 随后被从中衍生的。 克隆的生产率分布强烈偏向高生产者,遗传和表达稳定性始终如一。 通过避免差的整合率,联系机形成,有害的转基因重组,低平均表达水平,不可预测的产品质量和非致力学重组方法的不一致遗传稳定性,跨越式提供了几种对降低风险计划的机会,并降低了时间表和资源 。

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