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Development a scalable production process for truncated human papillomavirus type-6 L1 protein using WAVE Bioreactor and hollow fiber membrane

机译:使用WAVE Bioreactor和中空纤维膜开发截短型人乳头瘤病毒6型L1蛋白的可扩展生产工艺

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Here, we describe a process for expression, purification, and characterization of truncated human papillomavirus type-6 (HPV-6) L1 virus-like particles (VLPs). The scalable cultivation process in a WAVE Bioreactor at the 10-L scale was optimized to express HPV-6 L1 VLPs using the baculovirus insect expression system. A hollow fiber membrane system was used for the integrated operation, including concentration, diafiltration, extraction, and clarification. The HPV-6 L1 protein was further purified by anion-exchange chromatography and hydrophobic chromatography. The HPV-6 L1 protein could self-assemble into VLPs with a diameter of approximately 50-60 nm after removal of the reductant dithiothreitol (DTT). The final purified HPV-6 L1 VLPs product was characterized to estimate yield and purity, and exceeds the requirements for pharmaceutical-grade VLP vaccine. Immunization of mice demonstrated that the vaccine could elicit high titer neutralizing antibodies in vivo. This study confirms the feasibility of producing pharmaceutical-grade HPV type-6 L1 VLPs on an industrial scale for clinical trials.
机译:在这里,我们描述了一种表达,纯化和表征截短的人类6型乳头瘤病毒(HPV-6)L1病毒样颗粒(VLP)的过程。使用杆状病毒昆虫表达系统优化了WAVE生物反应器中10-L规模的可扩展培养过程,以表达HPV-6 L1 VLP。中空纤维膜系统用于集成操作,包括浓缩,渗滤,萃取和澄清。 HPV-6 L1蛋白通过阴离子交换色谱和疏水色谱进一步纯化。去除还原剂二硫苏糖醇(DTT)后,HPV-6 L1蛋白可以自组装成直径约为50-60 nm的VLP。最终纯化的HPV-6 L1 VLP产品的特征在于估计产量和纯度,并且超出了药物级VLP疫苗的要求。小鼠免疫证明该疫苗可在体内引发高滴度中和抗体。这项研究证实了以工业规模生产用于临床试验的药用级HPV 6型L1 VLP的可行性。

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