Department of Chemical Engineering, The Pennsylvania State University, University Park, Pennsylvania, USA.
Biotechnol Bioeng. 2024 Feb;121(2):710-718. doi: 10.1002/bit.28607. Epub 2023 Nov 23.
Virus filtration is a crucial step in ensuring the high levels of viral clearance required in the production of biotherapeutics produced in mammalian cells or derived from human plasma. Previous studies have reported that virus retention is often reduced in the presence of therapeutic proteins due to membrane fouling; however, the underlying mechanisms controlling this behavior are still not well understood. Experimental studies were performed with a single layer of the commercially available dual-layer Pegasus SV4 virus removal filter to more easily interpret the experimental results. Bacteriophage ФX174 was used as a model parvovirus, and human immunoglobulin (hIgG) and Bovine Serum Albumin (BSA) were used as model proteins. Data obtained with 5 g/L solutions of hIgG showed more than a 100-fold reduction in virus retention compared to that in the protein-free solution. Similar effects were seen with membranes that were pre-fouled with hIgG and then challenged with ФX174. The experimental data were well-described using an internal polarization model that accounts for virus capture and accumulation within the virus filter, with the hIgG nearly eliminating the irreversible virus capture while also facilitating the release of previously captured virus. These results provide important insights into the performance and validation of virus removal filters in bioprocessing.
病毒过滤是确保生产哺乳动物细胞或源自人血浆的生物疗法所需的高病毒清除水平的关键步骤。先前的研究报告称,由于膜污染,治疗性蛋白的存在常常会降低病毒保留率;然而,控制这种行为的潜在机制仍未得到很好的理解。本研究使用市售的双层 Pegasus SV4 病毒去除过滤器的单层进行实验,以便更轻松地解释实验结果。噬菌体 ФX174 被用作模型微小病毒,人免疫球蛋白(hIgG)和牛血清白蛋白(BSA)被用作模型蛋白。与无蛋白溶液相比,5g/L 的 hIgG 溶液中的病毒保留率降低了 100 多倍。用 hIgG 预先污染的膜然后用 ФX174 进行挑战,也观察到了类似的效果。使用内部极化模型很好地描述了实验数据,该模型考虑了病毒在病毒过滤器中的捕获和积累,hIgG 几乎消除了不可逆的病毒捕获,同时也促进了先前捕获的病毒的释放。这些结果为生物加工中病毒去除过滤器的性能和验证提供了重要的见解。