Bioanalytical Science, Bristol-Myers Squibb, Princeton, NJ 08540, United States.
Bioanalytical Science, Bristol-Myers Squibb, Princeton, NJ 08540, United States.
J Immunol Methods. 2018 Nov;462:34-41. doi: 10.1016/j.jim.2018.08.003. Epub 2018 Aug 9.
Biological therapeutics are foreign antigens and can potentially induce immune response resulting in the formation of anti-drug antibodies (ADA), which in turn may lead to a wide range of side effects. Neutralizing Ab (NAb) is a subset of ADA that can bind to the pharmacological activity regions of therapeutic to inhibit or complete neutralize its clinical efficacy. A cell-based functional NAb assay is preferred to characterize its neutralization activity. However, cell-based NAb assays are often vulnerable to drug interference, as well as interference from numerous serum factors, including but not limited to growth factors and disease-related cytokines. Bead Extraction with Acid Dissociation (BEAD) has been successfully applied to remove circulating drug and/or other interfering factors from human serum samples, thereby enriching for ADA/NAb. However, the harsh acid used in the extraction procedure can cause irreversible denaturing of NAb and lead to underestimated NAb measurement. Herein we describe a new approach when acid-dissociation is not optimal for a PEGylated domain antibody (Ab). We further demonstrate that heating at 62 °C can not only dissociate drug/ADA/NAb immune complex but also selectively and irreversibly denature domain Ab drug due to much lower thermal stability of the domain Ab, when compared to that of full antibodies. The irreversible denaturing of the drug favors the formation of an immune complex between ADA/NAb and the added biotinylated drug thus increasing the recovery of ADA/NAb from samples. We call this new procedure Bead Extraction with Heat Dissociation (BEHD), which can potentially be applied to other NAb assays that have poor compatibility with acid dissociation.
生物疗法是外来抗原,有可能引起免疫反应,导致产生抗药物抗体 (ADA),而抗药物抗体又可能导致广泛的副作用。中和抗体 (NAb) 是 ADA 的一个子集,能够与治疗药物的药理活性区域结合,抑制或完全中和其临床疗效。细胞功能性 NAb 测定法是用于表征其中和活性的首选方法。然而,细胞基 NAb 测定法通常容易受到药物干扰以及许多血清因素的干扰,包括但不限于生长因子和与疾病相关的细胞因子。酸解离珠粒提取 (BEAD) 已成功用于从人血清样品中去除循环药物和/或其他干扰因素,从而富集 ADA/NAb。然而,提取过程中使用的强酸会导致 NAb 不可逆变性,从而导致 NAb 测量值低估。在此,我们描述了一种新方法,当酸解离不适合聚乙二醇化域抗体 (Ab) 时,可以使用该方法。我们进一步证明,与完整抗体相比,加热至 62°C 不仅可以解离药物/ADA/NAb 免疫复合物,而且由于域 Ab 的热稳定性低得多,还可以选择性和不可逆地使域 Ab 药物变性。药物的不可逆变性有利于 ADA/NAb 与添加的生物素化药物之间形成免疫复合物,从而增加从样品中回收 ADA/NAb 的量。我们将这种新方法称为热解离珠粒提取 (BEHD),它可能适用于与酸解离不兼容的其他 NAb 测定法。