2023 年病毒清除研讨会论文集》,会议 2:病毒清除战略与案例研究。

Q3 Medicine
Frank Kohne, Astrid Schwantes
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引用次数: 0

摘要

本环节讨论生物制药病毒清除研究的合理设计,包括重组蛋白(如单克隆抗体),以及本次研讨会新增的腺相关病毒(AAV)载体的病毒清除。在重组蛋白方面,过去几十年积累了大量数据集,这些数据集可用于加速产品工艺开发和简化病毒清除研究。如何在病毒清除验证中利用先验知识,以及如何将先验知识用于风险评估工具,以决定在产品开发过程中是否有必要进行额外的病毒清除研究,将在本次会议的三个专题报告中讨论。其中包括针对 CG-110 等新型洗涤剂的先验预期设计和验证数据生成,以建立一个平台数据集,在未来的市场应用中作为先验知识使用。另一个报告研究了新开发的疏水相互作用色谱(HIC)树脂的病毒去除机制,并展示了在确定的工艺范围内适当减少高疏水性抗体中的逆转录病毒和杂质的效果,而最近的 HIC 树脂对病毒的减少效果一般到较差。最后两个报告涉及 AAV 的病毒清除方法,随着 ICH Q5A 修订版的批准,这将成为强制性规定。可以在 AAV 载体的生产过程中采用适当的病毒清除和病毒灭活程序,包括病毒过滤、病毒灭活(如热灭活)、亲和色谱法和阴离子交换色谱法。在了解产品特性和工艺条件的情况下,热处理步骤甚至可以成为 AAV 产品腺病毒辅助病毒灭活的有力步骤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Proceedings of the 2023 Viral Clearance Symposium, Session 2: Viral Clearance Strategy and Case Studies.

This session deals with the rational design of viral clearance studies for biopharmaceuticals including recombinant proteins such as monoclonal antibodies and, as new in scope of the symposium, also viral clearance for adeno-associated viral (AAV) vectors. For recombinant proteins, large datasets were accumulated over the last decades and are intended to be used for accelerated product process development and streamlining of viral clearance studies. How to utilize prior knowledge in viral clearance validation and how it can be used in a risk assessment tool to decide whether additional virus clearance studies are necessary during product development is being addressed by three of the presentations of this session. This also includes an a priori intended design and generation of validation data for a new kind of detergent such as CG-110, to build up a platform dataset to be used as prior knowledge in future marketing application. Another presentation investigates the virus removal mechanism of a newly developed hydrophobic interaction chromatography (HIC) resin and demonstrates for highly hydrophobic antibodies appropriate reduction for a retrovirus and impurities in a defined process range in contrast to the moderate to poor virus reduction of recent HIC resins. The last two presentations deal with virus clearance approaches for AAV, which will become mandatory with approval of the ICH Q5A revision. Appropriate virus removal and virus inactivation procedures can be implemented into the manufacturing processes of AAV vectors including viral filtration, viral inactivation (e.g., heat inactivation), affinity chromatography, and anion-exchange chromatography with which it seems possible to achieve a good clearance for helper and also adventitious viruses. The heat treatment step can be even a robust step for adenovirus helper inactivation for AAV products when product characteristics and process conditions are understood.

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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
34
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