Regeneron Pharmaceuticals, Bioanalytical Sciences, 777 Old Saw Mill River Rd, NY, 10591, Tarrytown, United States of America.
Regeneron Pharmaceuticals, Therapeutic Proteins, 777 Old Saw Mill River Rd, NY, 10591, Tarrytown, United States of America.
AAPS J. 2022 Jun 21;24(4):76. doi: 10.1208/s12248-022-00724-y.
A cell-based assay was developed to detect neutralizing anti-drug antibodies (NAbs) against odronextamab, a CD20xCD3 bispecific monoclonal antibody (mAb) under investigation for treatment of CD20+ B cell malignancies. In this assay, odronextamab bridges between two cell types, CD20-expressing HEK293 cells and CD3-expressing Jurkat T cells that generate a luciferase signal upon CD3 clustering. Patient samples containing NAbs directed to either arm of the bispecific drug block the odronextamab bridge formation between the cell lines thus preventing the generation of the luciferase signal. We determined that other anti-CD20 therapeutics also block bridge formation, resulting in false-positive results. In patient samples from odronextamab clinical trials, approximately 30% of baseline samples had a strong false-positive NAb signal that correlated with the presence of prior rituximab (anti-CD20) therapy. We determined that rituximab interference can be minimized by the addition of anti-rituximab antibodies in the NAb assay. Understanding and mitigating the impact of prior biologic exposure is increasingly important for implementing a successful bioanalytical strategy to support clinical drug development, especially in the immuno-oncology field. Odronextamab neutralizing antibody assay, interference, and mitigation. A Design of the odronextamab neutralizing antibody (NAb) assay where anti-CD20xCD3 drug bridges between CD20-expressing HEK293 cells and Jurkat T cells expressing an NFAT response element and luciferase reporter. True NAb prevents odronextamab from bridging between target and effector cells, thus preventing the expression of luciferase. B Interference with odronextamab from other anti-CD20 therapeutic antibodies (e.g., rituximab) from prior disease treatment generates a false-positive NAb result. Assay interference can be mitigated with an anti-idiotypic antibody against the interfering therapy.
建立了一种基于细胞的测定法来检测针对 odronextamab 的中和抗体 (NAb),odronextamab 是一种正在研究用于治疗 CD20+ B 细胞恶性肿瘤的 CD20xCD3 双特异性单克隆抗体 (mAb)。在该测定法中,odronextamab 在表达 CD20 的 HEK293 细胞和表达 CD3 的 Jurkat T 细胞这两种细胞类型之间形成桥接,当 CD3 聚集时会产生荧光素酶信号。含有针对双特异性药物任一侧臂的 NAb 的患者样本会阻断细胞系之间的 odronextamab 桥接形成,从而阻止荧光素酶信号的产生。我们发现其他抗 CD20 治疗药物也会阻断桥接形成,导致假阳性结果。在 odronextamab 临床试验的患者样本中,约 30%的基线样本具有强烈的假阳性 NAb 信号,与先前利妥昔单抗(抗 CD20)治疗的存在相关。我们发现,通过在 NAb 测定中添加抗利妥昔单抗抗体,可以最小化利妥昔单抗的干扰。了解和减轻先前生物暴露的影响对于实施成功的生物分析策略以支持临床药物开发越来越重要,尤其是在免疫肿瘤学领域。odronextamab 中和抗体测定、干扰和缓解。A odronextamab 中和抗体 (NAb) 测定的设计,其中抗 CD20xCD3 药物在表达 NFAT 反应元件和荧光素酶报告基因的 CD20 表达 HEK293 细胞和 Jurkat T 细胞之间形成桥接。真正的 NAb 可防止 odronextamab 在靶细胞和效应细胞之间桥接,从而阻止荧光素酶的表达。B 来自先前疾病治疗的其他抗 CD20 治疗性抗体(例如利妥昔单抗)与 odronextamab 相互干扰,产生假阳性 NAb 结果。可以使用针对干扰治疗的抗独特型抗体来减轻测定干扰。