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抗药物抗体稳定性测试的 EBF 建议;从抗疫苗抗体稳定性研究中吸取的经验教训。

EBF recommendation for stability testing of anti-drug antibodies; lessons learned from anti-vaccine antibody stability studies.

作者信息

Pihl Susanne, Michaut Lydia, Hendriks Jenny, Loebbert Ralf, Ryding Janka, Nemansky Martin, Vermet Laurent, Companjen Arjen

机构信息

H Lundbeck A/S, Department of Bioanalysis, Drug Development ADME, H Lundbeck A/S, Ottiliavej 7-9, DK-2500 Valby, Denmark.

出版信息

Bioanalysis. 2014 May;6(10):1409-13. doi: 10.4155/bio.14.95.

Abstract

Long- and short-term stability testing of the analyte is one of the key parameters in bioanalytical method validation in support of pharmacokinetics. However, for immunogenicity testing, the scientific rationale for long- and short-term stability testing on quality control samples most often spiked with polyclonal antibody raised in a different species should be questioned. Therefore, the European Bioanalysis Forum (EBF) formed a Topic Team to discuss the scientific rationale for stability testing of anti-drug antibodies (ADAs). A review of EBF member companies' experience on ADA stability and on anti-vaccine antibodies from vaccine projects was the basis of this discussion. EBF recommends to perform short-term stability testing of the positive control, but not to perform long-term stability testing of ADAs in nonclinical and clinical studies.

摘要

分析物的长期和短期稳定性测试是支持药代动力学的生物分析方法验证中的关键参数之一。然而,对于免疫原性测试,对通常添加了在不同物种中产生的多克隆抗体的质量控制样品进行长期和短期稳定性测试的科学依据常常受到质疑。因此,欧洲生物分析论坛(EBF)成立了一个专题小组来讨论抗药物抗体(ADA)稳定性测试的科学依据。对EBF成员公司在ADA稳定性以及疫苗项目中抗疫苗抗体方面的经验进行回顾是此次讨论的基础。EBF建议对阳性对照进行短期稳定性测试,但在非临床和临床研究中不对ADA进行长期稳定性测试。

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