Symphogen A/S, Elektrovej, Building 375, DK-2800, Lyngby, Denmark.
Mol Biotechnol. 2010 Jul;45(3):257-66. doi: 10.1007/s12033-010-9270-9.
We have previously described the development and implementation of a strategy for production of recombinant polyclonal antibodies (rpAb) in single batches employing CHO cells generated by site-specific integration, the Sympress I technology. The Sympress I technology is implemented at industrial scale, supporting a phase II clinical development program. Production of recombinant proteins by site-specific integration, which is based on incorporation of a single copy of the gene of interest, makes the Sympress I technology best suited to support niche indications. To improve titers while maintaining a cost-efficient, highly reproducible single-batch manufacturing mode, we have evaluated a number of different approaches. The most successful results were obtained using random integration in a new producer cell termed ECHO, a CHO DG44 cell derivative engineered for improved productivity at Symphogen. This new expression process is termed the Sympress II technology. Here we describe proof-of-principle data demonstrating the feasibility of the Sympress II technology for single-batch rpAb manufacturing using two model systems each composed of six target-specific antibodies. The compositional stability and the batch-to-batch reproducibility of rpAb produced by the ECHO cells were at least as good as observed previously using site-specific integration technology. Furthermore, the new process had a significant titer increase.
我们之前描述了一种策略的开发和实施,该策略用于通过定点整合(Sympress I 技术)生成的 CHO 细胞单次批量生产重组多克隆抗体(rpAb)。Sympress I 技术已在工业规模上实施,支持 II 期临床开发计划。基于目的基因单拷贝的定点整合生产重组蛋白使 Sympress I 技术最适合支持利基适应症。为了在保持成本效益、高度可重复的单次批量生产模式的同时提高滴度,我们评估了许多不同的方法。最成功的结果是使用称为 ECHO 的新型生产细胞中的随机整合获得的,ECHO 是一种为提高 Symphogen 生产力而设计的 CHO DG44 细胞衍生物。这种新的表达过程被称为 Sympress II 技术。在这里,我们描述了使用两种由六个靶特异性抗体组成的模型系统证明 Sympress II 技术用于单次批量 rpAb 制造的原理验证数据。使用 ECHO 细胞生产的 rpAb 的组成稳定性和批间重现性至少与以前使用定点整合技术观察到的一样好。此外,新工艺的滴度显著提高。