基于机制的建模方法量化免疫原性对药物开发中治疗蛋白药代动力学的影响。

IF 3 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Paridhi Gupta, Josiah T. Ryman, Vibha Jawa, Bernd Meibohm
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引用次数: 0

摘要

在临床前和临床研究中,治疗性蛋白的使用可导致针对治疗性蛋白的抗药物抗体的形成。抗药抗体的形成可能改变治疗蛋白的药代动力学,降低其血浆浓度,增加暴露变异性,并可能导致疗效丧失和不良事件。为了定量地了解抗药物抗体对治疗性蛋白的浓度-时间谱的影响,以及制定有效的策略来减轻其在治疗性蛋白的临床前和临床开发中的影响,已经建立了数学模型来表征治疗性蛋白的药代动力学及其在体内被抗药物抗体调节。在此,我们回顾了几种不同的基于机制的建模框架,总结了它们预测免疫原性效应的方法,并探讨了每种模型的优点和局限性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mechanism-Based Modeling Approaches to Quantify the Effect of Immunogenicity on the Pharmacokinetics of Therapeutic Proteins in Drug Development

Mechanism-Based Modeling Approaches to Quantify the Effect of Immunogenicity on the Pharmacokinetics of Therapeutic Proteins in Drug Development

Mechanism-Based Modeling Approaches to Quantify the Effect of Immunogenicity on the Pharmacokinetics of Therapeutic Proteins in Drug Development

Mechanism-Based Modeling Approaches to Quantify the Effect of Immunogenicity on the Pharmacokinetics of Therapeutic Proteins in Drug Development

Mechanism-Based Modeling Approaches to Quantify the Effect of Immunogenicity on the Pharmacokinetics of Therapeutic Proteins in Drug Development

Therapeutic protein administration in both preclinical and clinical studies can result in the formation of anti-drug antibodies against the therapeutic protein. Anti-drug antibody formation may alter the pharmacokinetics of the therapeutic protein, reduce its plasma concentrations, increase exposure variability, and may lead to a loss of efficacy and adverse events. In an effort to quantitatively understand the effect of anti-drug antibodies on the concentration-time profile of a therapeutic protein, as well as develop effective strategies to mitigate its impact in the preclinical and clinical development of therapeutic proteins, mathematical models have been developed to characterize the therapeutic protein pharmacokinetics and its modulation by anti-drug antibodies in vivo. Here, we review several different mechanism-based modeling frameworks, summarize their approaches to predict immunogenicity effects, and explore the merits and limitations of each model.

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来源期刊
CiteScore
5.00
自引率
11.40%
发文量
146
审稿时长
8 weeks
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