Department of Analytical Sciences, BioPharmaceuticals Development, BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, MD, USA.
Department of Analytical Sciences, BioPharmaceuticals Development, BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, MD, USA.
J Immunol Methods. 2021 Sep;496:113099. doi: 10.1016/j.jim.2021.113099. Epub 2021 Jul 2.
Bispecific antibodies (BsAbs) are engineered to simultaneously bind two different antigens, and offer promising clinical outcomes for various diseases. The dual binding properties of BsAbs may enable superior efficacies and/or potencies compared to standard monoclonal antibodies (mAbs) or combination mAb therapies. Characterizing BsAb binding properties is critical during biotherapeutic development, where data is leveraged to predict efficacy and potency, assess critical quality attributes and improve antibody design. Traditional single-target, single-readout approaches (e.g., ELISA) have limited usefulness for interpreting complex bispecific binding, and double the benchwork. To address these deficiencies, we developed and implemented a new dual-target/readout binding assay that accurately dissects the affinities of both BsAb binding domains directly and simultaneously. This new assay uses AlphaPlex® technology, which eliminates traditional ELISA wash steps and can be miniaturized for automated workflows. The optimized BsAb AlphaPlex assay demonstrates 99-107% accuracy within a 50-150% linear range, and detected >50% binding degradation from photo- and thermal stress conditions. To the best of our knowledge, this is the first instance of a dual-target/readout BsAb AlphaPlex assay with GMP-suitable linear range, accuracy, specificity, and stability-indicating properties. As a highly customizable and efficient assay, BsAb AlphaPlex may be applicable to numerous bispecific formats and/or co-formulations against a variety of antigens beyond the clinical therapeutic space.
双特异性抗体 (BsAbs) 是经过设计可同时结合两种不同抗原的,为各种疾病提供了有前途的临床结果。BsAbs 的双重结合特性可能使它们与标准单克隆抗体 (mAbs) 或联合 mAb 疗法相比具有更好的疗效和/或效力。在生物治疗药物开发过程中,表征 BsAb 的结合特性非常重要,数据可用于预测疗效和效力、评估关键质量属性和改进抗体设计。传统的单靶标、单读值方法(例如 ELISA)对于解释复杂的双特异性结合非常有限用,并且需要两倍的工作量。为了解决这些缺陷,我们开发并实施了一种新的双靶标/读值结合测定法,该方法可以直接和同时准确剖析 BsAb 结合结构域的亲和力。该新测定法使用 AlphaPlex®技术,消除了传统 ELISA 的洗涤步骤,并可缩小规模以实现自动化工作流程。优化的 BsAb AlphaPlex 测定法在 50-150%的线性范围内的准确度为 99-107%,并检测到 >50%的光和热应激条件下的结合降解。据我们所知,这是首次具有 GMP 适用线性范围、准确度、特异性和稳定性指示特性的双靶标/读值 BsAb AlphaPlex 测定法。作为一种高度可定制和高效的测定法,BsAb AlphaPlex 可能适用于许多双特异性形式和/或针对多种抗原的联合配方,超出了临床治疗领域。