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Mol Biotechnol ; 45(3): 257-66, 2010 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20306237

RESUMO

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.


Assuntos
Anticorpos/metabolismo , Biotecnologia/métodos , Técnicas de Cultura de Células/métodos , Proteínas Recombinantes/biossíntese , Animais , Anticorpos/genética , Anticorpos/imunologia , Células CHO , Células Clonais/metabolismo , Clonagem Molecular/métodos , Cricetinae , Cricetulus , Vetores Genéticos , Humanos , Engenharia de Proteínas , Proteínas Recombinantes/genética , Proteínas Recombinantes/imunologia , Vírus Sinciciais Respiratórios/imunologia , Vacínia/imunologia
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