Aoyama Muneo, Mano Yuji
Global Drug Metabolism and Pharmacokinetics, Eisai Co., Ltd., Tokodai 5-1-3, Tsukuba, Ibaraki 300-2635, Japan.
Global Drug Metabolism and Pharmacokinetics, Eisai Co., Ltd., Tokodai 5-1-3, Tsukuba, Ibaraki 300-2635, Japan; Laboratory of Genomics-based Drug Discovery, Faculty of Medicine, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tennodai 1-1-1, Tsukuba, Ibaraki 305-8575, Japan.
J Pharmacol Toxicol Methods. 2023 Nov-Dec;124:107470. doi: 10.1016/j.vascn.2023.107470. Epub 2023 Sep 7.
E6011, a humanized anti-fractalkine monoclonal antibody, is under development for the treatment of various inflammatory diseases, such as rheumatoid arthritis. Therapeutic antibodies may induce production of anti-drug antibodies (ADA) that may deteriorate efficacy and/or enhance immunogenic reaction. It is important to have an ADA assay to understand the characteristics of biotherapeutics under development. A simple and reproducible assay has thus been developed for the determination of ADA against E6011 in monkey and human serum by electrochemiluminescence (ECL) detection. An immune-complex of biotinylated E6011, ADA, and ruthenium-labeled E6011 was attached to avidin-coated wells for ECL signal detection. Screening and confirmatory cutpoints were determined to judge negative or positive ADA. Sensitivity of ADA was 1.61 and 1.34 ng/mL in monkey and human serum, respectively. Accuracy and precision of the assay were within ±20% and 20%, respectively. Drug tolerance of the assay in monkey and human sera was ensured up to 100 and 1000 μg/mL E6011 at the surrogate ADA levels of 1 and 4 μg/mL, respectively. The developed assay was successfully applied to ADA quantification in monkeys and humans in support of immunogenicity assessments.
人源化抗 fractalkine 单克隆抗体 E6011 正在研发用于治疗多种炎症性疾病,如类风湿性关节炎。治疗性抗体可能会诱导产生抗药物抗体(ADA),这可能会降低疗效和/或增强免疫反应。开展 ADA 检测对于了解正在研发的生物治疗药物的特性很重要。因此,已开发出一种简单且可重复的检测方法,通过电化学发光(ECL)检测来测定猴血清和人血清中针对 E6011 的 ADA。将生物素化的 E6011、ADA 和钌标记的 E6011 的免疫复合物附着到抗生物素蛋白包被的孔中进行 ECL 信号检测。确定筛选和确证切点以判断 ADA 阴性或阳性。ADA 在猴血清和人血清中的灵敏度分别为 1.61 和 1.34 ng/mL。该检测方法的准确度和精密度分别在±20%和 20%以内。在替代 ADA 水平分别为 1 和 4 μg/mL 时,该检测方法在猴血清和人血清中的药物耐受性分别确保高达 100 和 1000 μg/mL 的 E6011。所开发的检测方法已成功应用于猴和人的 ADA 定量分析,以支持免疫原性评估。