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利用药代动力学分析数据对中和性抗药物抗体进行间接评估。

Indirect assessment of neutralizing anti-drug antibodies utilizing pharmacokinetic assay data.

作者信息

Vettermann Christian, Ortiz Jessica, Lee Stephanie, Sanchez Sergio, Victor Hannah P, Ma Mark, Heath Timothy, Gupta Shalini

机构信息

Bioanalytical Sciences, Department of Pharmacokinetics and Drug Metabolism, Amgen, Inc., One Amgen Center Drive, Thousand Oaks, CA 91320, United States.

Bioanalytical Sciences, Department of Pharmacokinetics and Drug Metabolism, Amgen, Inc., One Amgen Center Drive, Thousand Oaks, CA 91320, United States.

出版信息

J Immunol Methods. 2016 Feb;429:28-38. doi: 10.1016/j.jim.2015.12.010. Epub 2015 Dec 19.

Abstract

Neutralizing anti-drug antibodies (NAbs) can adversely impact efficacy and safety of biologic therapeutics. However, current assay formats to detect NAbs are limited in their use during the dosing phase due to interference by circulating drug, resulting in low drug tolerance. To improve the drug tolerance for NAb detection, an alternative approach for indirect NAb (iNAb) assessment was developed and qualified that uses a combination of pharmacokinetic (PK) assays to measure the serum concentrations of free and total drug. It is demonstrated that the ratio of free to total drug concentrations, referred to as F/T ratio, is a novel PK parameter that can indicate neutralizing activity in test samples. The iNAb assessment correctly identified NAb-positive samples with high drug concentrations that led to false negative results in a conventional NAb assay. Moreover, iNAb reliably distinguished between NAbs and non-neutralizing anti-drug antibodies over a wide range of concentrations. A proposal on how to deploy iNAb assessment within a broader immunogenicity testing strategy is presented.

摘要

中和抗药物抗体(NAbs)会对生物治疗药物的疗效和安全性产生不利影响。然而,由于循环药物的干扰,目前用于检测NAbs的检测方法在给药阶段的应用受到限制,导致药物耐受性较低。为了提高检测NAbs时的药物耐受性,开发并验证了一种间接NAb(iNAb)评估的替代方法,该方法使用药代动力学(PK)检测的组合来测量游离药物和总药物的血清浓度。结果表明,游离药物浓度与总药物浓度之比,即F/T比,是一个新的PK参数,可指示测试样品中的中和活性。iNAb评估正确识别了高药物浓度下导致传统NAb检测出现假阴性结果的NAb阳性样品。此外,iNAb在很宽的浓度范围内可靠地区分了NAbs和非中和抗药物抗体。本文还提出了关于如何在更广泛的免疫原性检测策略中应用iNAb评估的建议。

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