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“高危”宿主细胞蛋白(HCPs):多公司合作视角。

"High-risk" host cell proteins (HCPs): A multi-company collaborative view.

机构信息

GlaxoSmithKline, CMC Analytical, Structure & Function Characterization, Collegeville, Pennsylvania, USA.

Regeneron Pharmaceuticals Inc., Protein Biochemistry, Tarrytown, New York, USA.

出版信息

Biotechnol Bioeng. 2021 Aug;118(8):2870-2885. doi: 10.1002/bit.27808. Epub 2021 May 31.

DOI:10.1002/bit.27808
PMID:33930190
Abstract

Host cell proteins (HCPs) are process-related impurities that may copurify with biopharmaceutical drug products. Within this class of impurities there are some that are more problematic. These problematic HCPs can be considered high-risk and can include those that are immunogenic, biologically active, or enzymatically active with the potential to degrade either product molecules or excipients used in formulation. Some have been shown to be difficult to remove by purification. Why should the biopharmaceutical industry worry about these high-risk HCPs? What approach could be taken to understand the origin of its copurification and address these high-risk HCPs? To answer these questions, the BioPhorum Development Group HCP Workstream initiated a collaboration among its 26-company team with the goal of industry alignment around high-risk HCPs. The information gathered through literature searches, company experiences, and surveys were used to compile a list of frequently seen problematic/high-risk HCPs. These high-risk HCPs were further classified based on their potential impact into different risk categories. A step-by-step recommendation is provided for establishing a comprehensive control strategy based on risk assessments for monitoring and/or eliminating the known impurity from the process that would be beneficial to the biopharmaceutical industry.

摘要

宿主细胞蛋白(HCPs)是与生物制药产品共纯化的工艺相关杂质。在这类杂质中,有一些更为棘手。这些有问题的 HCPs 可被视为高风险,其中包括那些具有免疫原性、生物活性或酶活性的杂质,有潜在能力降解产品分子或制剂中使用的赋形剂。有些已被证明难以通过纯化去除。为什么生物制药行业要担心这些高风险的 HCPs?可以采取什么方法来了解其共纯化的来源并解决这些高风险的 HCPs?为了回答这些问题,BioPhorum 开发小组 HCP 工作组启动了其 26 家公司团队之间的合作,旨在围绕高风险 HCPs 达成行业一致。通过文献检索、公司经验和调查收集的信息被用于编制一份常见的有问题/高风险 HCPs 清单。根据其潜在影响,这些高风险 HCPs 进一步分为不同的风险类别。为建立基于风险评估的全面控制策略提供了分步建议,用于监测和/或从工艺中消除已知杂质,这将有益于生物制药行业。

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