基于细胞的人血清中阿达木单抗抗体中和功能检测方法的开发与验证

M. Nikiforova, I. A. Valouev, A. V. Petrov, E. Beketov, I. E. Shokhin
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摘要

简介阿达木单抗是一种完全人源化的单克隆抗体,是一种肿瘤坏死因子(TNFα)灭活剂,可用于治疗多种自身免疫性疾病,如类风湿性关节炎和其他最常见的炎症性关节病(强直性脊柱炎、银屑病关节炎)。尽管阿达木单抗的疗效已得到证实,但仍有发生不良反应的风险,这与抗药性抗体(包括中和抗体)的形成有关。目前,评估和鉴定中和抗体已成为开发新药物和生物仿制药临床试验的重要组成部分。本研究旨在开发和验证基于细胞的功能性方法,用于测定人血清中的抗阿达木单抗中和抗体。为了测定中和性抗阿达木单抗抗体,我们使用了L-929细胞系。L-929是一种对TNFα介导的细胞凋亡敏感的细胞系;中和抗体与阿达木单抗相互作用,导致TNFα介导的细胞毒性。细胞毒性的测定使用了一种可作为氧化还原指示剂的芳香族化合物--雷沙祖林。所开发的方法在切点、选择性、灵敏度、精确度、特异性和稳定性(短期和长期)方面都得到了验证。中和抗体测定方法开发的一个重要部分是选择 TNFα(4 纳克/毫升)和阿达木单抗(250 纳克/毫升)的浓度,以及确定所需的最小稀释度--该参数设定为 1:20。切点选择为 "浮动 "切点,校正因子(归一化因子)确定为 0.86。所开发方法的灵敏度估计为 108.9 纳克/毫升中和抗阿达木单抗抗体。所得结果可用于阿达木单抗免疫原性评估(包括临床试验)中抗阿达木单抗中和抗体的测定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development and Validation of the Cell-based Functional Method for Neutralizing Anti-adalimumab Antibodies Detection in Human Serum
Introduction. Adalimumab, a fully humanized monoclonal antibody, is a tumor necrosis factor (TNFα) inactivator that is used against a number of autoimmune diseases such as rheumatoid arthritis and other most common inflammatory arthropathies (ankylosing spondylitis, psoriatic arthritis). Despite the proven efficacy of adalimumab treatment, there is a risk of adverse events, tied up with the formation of anti-drug antibodies, including neutralizing antibodies. Currently, the evaluation and characterization of neutralizing antibodies has become an important part of clinical trials in the development of new drugs and biosimilars.Aim. The aim of this study is to develop and validate the cell-based functional method for neutralizing anti-adalimumab antibodies determination in human serum.Materials and methods. For determination of neutralizing anti-adalimumab antibodies, the cell line L-929 has been employed. L-929 is a cell line sensitive to the TNFα-mediated apoptosis; the neutralizing antibodies interact with adalimumab that leads to TNFα-mediated cytotoxicity. Cytotoxicity was measured using resazurin, an aromatic compound that is a redox indicator.Results and discussion. The developed method was validated for cut point, selectivity, sensitivity, precision, specificity and stability (short- and long-term). An important part of a method development for determining neutralizing antibodies is the selection of concentrations of TNFα (4 ng/ml) and adalimumab (250 ng/ml), as well as determining the minimum required dilution – this parameter is established as 1 : 20. Cut point was chosen as a «floating» cut point, and a correction factor (normalization factor) was determined equal to 0,86. The sensitivity of the developed method was estimated at 108,9 ng/ml of neutralizing anti-adalimumab antibodies.Conclusion. The obtained results can be applied for determining anti-adalimumab neutralizing antibodies in the assessment of the adalimumab immunogenicity, including clinical trials.
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