Affinity Capture Elution Coupled with Cell-based Cyclic Adenosine Monophosphate Assay as a Platform Method for Detection of Neutralizing Antibodies to Incretin Molecules.

IF 3.7 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Nichole A Reynolds, Yan Q Chen, Richard E Higgs, Boris Calderon, Jeff W Cramer, Nicoletta Bivi, Michael E Hodsdon, Heather A Bullock, Travis E Shockley, Victoria L Peek, Justin K Mack, Deven Lemen, Victoria Copeland, Andrea Ferrante, Robert J Konrad, Garrett Mullins, Yi Wen
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引用次数: 0

Abstract

Formation of anti-drug antibodies (ADA) and, in particular, neutralizing antibodies (NAb), is a major risk to the development of biotherapeutics. Cell-based assays, which can reflect the mechanistic interactions among the drug, target, and NAb, are often most suitable for the detection of NAb. We report the development and validation of cell-based platform assays for a class of incretin molecules. An affinity capture elution step was employed to improve drug tolerance of a cell-based cyclic adenosine monophosphate (cAMP) assay. Assay conditions and procedures, including acid elution, cell density, and TAG labeled cAMP (cAMP-TAG) incubation time and concentration, were thoroughly optimized. Delta percent (Δ%) Neutralization was used to reduce assay variability during validation and sample analysis. This platform method has been applied to several incretin molecules and has demonstrated desired sensitivity, drug tolerance, and robustness.

亲和捕获洗脱结合细胞环磷酸腺苷测定作为检测肠促胰岛素分子中和抗体的平台方法。
抗药物抗体(ADA),特别是中和抗体(NAb)的形成是生物治疗发展的主要风险。基于细胞的检测方法可以反映药物、靶标和NAb之间的机制相互作用,通常最适合检测NAb。我们报告了一类肠促胰岛素分子的基于细胞的平台分析的开发和验证。采用亲和捕获洗脱步骤来提高基于细胞的环磷酸腺苷(cAMP)试验的药物耐受性。实验条件和程序,包括酸洗脱、细胞密度、TAG标记的cAMP (cAMP-TAG)孵育时间和浓度,进行了彻底优化。Δ百分比(Δ%)中和用于减少验证和样品分析期间的测定变异性。该平台方法已应用于几种肠促胰岛素分子,并表现出良好的敏感性、耐受性和鲁棒性。
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来源期刊
AAPS Journal
AAPS Journal 医学-药学
CiteScore
7.80
自引率
4.40%
发文量
109
审稿时长
1 months
期刊介绍: The AAPS Journal, an official journal of the American Association of Pharmaceutical Scientists (AAPS), publishes novel and significant findings in the various areas of pharmaceutical sciences impacting human and veterinary therapeutics, including: · Drug Design and Discovery · Pharmaceutical Biotechnology · Biopharmaceutics, Formulation, and Drug Delivery · Metabolism and Transport · Pharmacokinetics, Pharmacodynamics, and Pharmacometrics · Translational Research · Clinical Evaluations and Therapeutic Outcomes · Regulatory Science We invite submissions under the following article types: · Original Research Articles · Reviews and Mini-reviews · White Papers, Commentaries, and Editorials · Meeting Reports · Brief/Technical Reports and Rapid Communications · Regulatory Notes · Tutorials · Protocols in the Pharmaceutical Sciences In addition, The AAPS Journal publishes themes, organized by guest editors, which are focused on particular areas of current interest to our field.
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