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评估免疫原性检测的特异性。

Assessing specificity for immunogenicity assays.

作者信息

Swanson Steven J, Chirmule Narendra

机构信息

Clinical Immunology Department, Amgen Inc., One Amgen Center Drive, 30E-3-B, Thousand Oaks, CA 91320, USA.

出版信息

Bioanalysis. 2009 Jun;1(3):611-7. doi: 10.4155/bio.09.41.

Abstract

Developing sensitive and specific bioanalytical assays for measuring the immunogenicity of biological therapeutics has become an integral component of the drug-development process. The strategy for measuring these immune responses involves performing sensitive screening assays that are capable of detecting low levels of both low- and high-affinity antibodies. However, having sensitive assays inherently results in a certain rate of false-positivity. Hence, developing steps to determine specificity in these assays is important to confirm the presence of antidrug antibodies. The specificity assays are defined by the ability of an assay to score a positive result if the serum sample contains an antibody that can bind and/or neutralize the therapeutic protein. Here, we discuss the methodologies for determining specificity in the bioanalytical assays used for measuring antidrug antibodies. These methods will provide investigators and regulators with guidelines to develop and review assays to measure antidrug antibodies, which can specifically interfere with the actions of the drug and/or influence the safety profile of the therapeutic proteins.

摘要

开发用于测量生物治疗药物免疫原性的灵敏且特异的生物分析方法,已成为药物研发过程中不可或缺的一部分。测量这些免疫反应的策略包括进行灵敏的筛选试验,这些试验能够检测低水平的低亲和力和高亲和力抗体。然而,灵敏的试验本身会导致一定比例的假阳性。因此,制定确定这些试验特异性的步骤对于确认抗药物抗体的存在很重要。特异性试验由试验在血清样本含有能结合和/或中和治疗性蛋白质的抗体时给出阳性结果的能力来定义。在此,我们讨论用于测量抗药物抗体的生物分析试验中确定特异性的方法。这些方法将为研究人员和监管机构提供指导方针,以开发和审查用于测量抗药物抗体的试验,这些抗体可特异性干扰药物作用和/或影响治疗性蛋白质的安全性。

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