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新型亲和配体在慢病毒载体纯化中的应用。

Implementation of Novel Affinity Ligand for Lentiviral Vector Purification.

机构信息

IBET Instituto de Biologia Experimental e Tecnológica, Apartado 12, 2780-901 Oeiras, Portugal.

ITQB Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Avenida da República, 2780-157 Oeiras, Portugal.

出版信息

Int J Mol Sci. 2023 Feb 8;24(4):3354. doi: 10.3390/ijms24043354.

Abstract

The use of viral vectors as therapeutic products for multiple applications such as vaccines, cancer treatment, or gene therapies, has been growing exponentially. Therefore, improved manufacturing processes are needed to cope with the high number of functional particles required for clinical trials and, eventually, commercialization. Affinity chromatography (AC) can be used to simplify purification processes and generate clinical-grade products with high titer and purity. However, one of the major challenges in the purification of Lentiviral vectors (LVs) using AC is to combine a highly specific ligand with a gentle elution condition assuring the preservation of vector biological activity. In this work, we report for the first time the implementation of an AC resin to specifically purify VSV-G pseudotyped LVs. After ligand screening, different critical process parameters were assessed and optimized. A dynamic capacity of 1 × 10 total particles per mL of resin was determined and an average recovery yield of 45% was found for the small-scale purification process. The established AC robustness was confirmed by the performance of an intermediate scale providing an infectious particles yield of 54%, which demonstrates the scalability and reproducibility of the AC matrix. Overall, this work contributes to increasing downstream process efficiency by delivering a purification technology that enables high purity, scalability, and process intensification in a single step, contributing to time-to-market reduction.

摘要

病毒载体作为治疗产品,在疫苗、癌症治疗或基因治疗等多个领域的应用呈指数级增长。因此,需要改进制造工艺,以满足临床试验乃至商业化所需的大量功能性颗粒。亲和层析(AC)可用于简化纯化工艺,生成高滴度、高纯度的临床级产品。然而,使用 AC 从慢病毒载体(LVs)中进行纯化的主要挑战之一是,需要将高度特异性的配体与温和的洗脱条件相结合,以确保载体生物活性的保存。在这项工作中,我们首次报告了一种 AC 树脂的应用,该树脂可特异性地纯化 VSV-G 假型 LVs。经过配体筛选,评估并优化了不同的关键工艺参数。确定了树脂 1×10^10 个总颗粒/mL 的动态载量,小规模纯化过程的平均回收率为 45%。中间规模的性能证实了 AC 基质的稳健性,提供了 54%的感染性颗粒收率,证明了 AC 基质的可扩展性和重现性。总的来说,这项工作通过提供一种能够在单一步骤中实现高纯度、可扩展性和强化工艺的纯化技术,提高了下游工艺效率,有助于缩短上市时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ba/9966744/0928181b0c00/ijms-24-03354-g001.jpg

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