Institute of Bioprocess Engineering and Pharmaceutical Technology, University of Applied Sciences Mittelhessen, Wiesenstrasse 14, 35390 Giessen, Germany.
Institute for Transfusion Medicine, University Hospital Essen, University of Duisburg-Essen, Virchowstrasse 179, 45147 Essen, Germany.
Viruses. 2023 Sep 27;15(10):2013. doi: 10.3390/v15102013.
Yellow Fever (YF) is a severe disease that, while preventable through vaccination, lacks rapid intervention options for those already infected. There is an urgent need for passive immunization techniques using YF-virus-like particles (YF-VLPs). To address this, we successfully established a bioreactor-based production process for YF-VLPs, leveraging transient transfection and integrating Process Analytical Technology. A cornerstone of this approach was the optimization of plasmid DNA (pDNA) production to a yield of 11 mg/L using design of experiments. Glucose, NaCl, yeast extract, and a phosphate buffer showed significant influence on specific pDNA yield. The preliminary work for VLP-production in bioreactor showed adjustments to the HEK cell density, the polyplex formation duration, and medium exchanges effectively elevated transfection efficiencies. The additive Pluronic F-68 was neutral in its effects, and anti-clumping agents (ACA) adversely affected the transfection process. Finally, we established the stirred-tank bioreactor process with integrated dielectric spectroscopy, which gave real-time insight in relevant process steps, e.g., cell growth, polyplex uptake, and harvest time. We confirmed the presence and integrity of YF-VLP via Western blot, imaging flow cytometry measurement, and transmission electron microscopy. The YF-VLP production process can serve as a platform to produce VLPs as passive immunizing agents against other neglected tropical diseases.
黄热病(YF)是一种严重的疾病,虽然可以通过疫苗接种预防,但对于已经感染的人缺乏快速干预的选择。因此,迫切需要使用黄热病病毒样颗粒(YF-VLPs)的被动免疫技术。为了解决这个问题,我们成功地建立了基于生物反应器的 YF-VLPs 生产工艺,利用瞬时转染并整合了过程分析技术。该方法的一个基石是通过实验设计将质粒 DNA(pDNA)的产量优化至 11mg/L。葡萄糖、NaCl、酵母提取物和磷酸盐缓冲液对特定的 pDNA 产量有显著影响。在生物反应器中进行 VLP 生产的初步工作表明,调整 HEK 细胞密度、多聚物形成时间和培养基交换可以有效地提高转染效率。添加剂 Pluronic F-68 的效果呈中性,而抗结块剂(ACA)会对转染过程产生不利影响。最后,我们建立了带有集成介电光谱学的搅拌罐生物反应器工艺,该工艺可以实时洞察相关的工艺步骤,例如细胞生长、多聚物摄取和收获时间。我们通过 Western blot、成像流式细胞术测量和透射电子显微镜确认了 YF-VLP 的存在和完整性。YF-VLP 生产工艺可以作为生产针对其他被忽视的热带病的被动免疫制剂的 VLPs 的平台。