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通过经过验证的酶联免疫吸附测定法对PD-1/PD-L1抗体的药代动力学特征进行定量分析。

Quantification of Pharmacokinetic Profiles of PD-1/PD-L1 Antibodies by Validated ELISAs.

作者信息

Zalba Sara, Contreras-Sandoval Ana M, Martisova Eva, Debets Reno, Smerdou Christian, Garrido María Jesús

机构信息

Department of Pharmacy and Pharmaceutical Technology, School of Pharmacy, University of Navarra, 31008 Pamplona, Spain.

Department of Molecular Oncology, Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.

出版信息

Pharmaceutics. 2020 Jun 26;12(6):595. doi: 10.3390/pharmaceutics12060595.

Abstract

Immunotherapy has changed the paradigm of cancer treatments. In this way, several combinatorial strategies based on monoclonal antibodies (mAb) such as anti (a)-PD-1 or anti (a)-PD-L1 are often reported to yield promising clinical benefits. However, the pharmacokinetic (PK) behavior of these mAbs is a critical issue that requires selective analytical techniques. Indeed, few publications report data on a-PD1/a-PD-L1 exposure and its relationship with therapeutic or toxic effects. In this regard, preclinical assays allow the time profiles of antibody plasma concentrations to be characterized rapidly and easily, which may help to increase PK knowledge. In this study, we have developed and validated two in-house ELISAs to quantify a-PD-1 and a-PD-L1 in plasma collected from tumor-bearing mice. The linear range for the a-PD-1 assay was 2.5-125 ng/mL and 0.11-3.125 ng/mL for the a-PD-L1 assay, whereas the intra-and inter-day precision was lower than 20% for both analytes. The PK characterization revealed a significant decrease in drug exposure after administration of multiple doses. Plasma half-life for a-PD-1 was slightly shorter (22.3 h) than for a-PD-L1 (46.7 h). To our knowledge, this is the first reported preclinical ELISA for these immune checkpoint inhibitors, which is sufficiently robust to be used in different preclinical models. These methods can help to understand the PK behavior of these antibodies under different scenarios and the relationship with response, thus guiding the choice of optimal doses in clinical settings.

摘要

免疫疗法已经改变了癌症治疗的模式。通过这种方式,基于单克隆抗体(mAb)的几种联合策略,如抗(a)-PD-1或抗(a)-PD-L1,常常被报道能产生有前景的临床益处。然而,这些单克隆抗体的药代动力学(PK)行为是一个关键问题,需要选择性分析技术。实际上,很少有出版物报道关于a-PD1/a-PD-L1暴露及其与治疗或毒性效应关系的数据。在这方面,临床前试验能够快速且容易地对抗体血浆浓度的时间曲线进行表征,这可能有助于增加对药代动力学的了解。在本研究中,我们开发并验证了两种内部酶联免疫吸附测定法(ELISA),用于定量从荷瘤小鼠采集的血浆中的a-PD-1和a-PD-L1。a-PD-1测定法的线性范围为2.5 - 125 ng/mL,a-PD-L1测定法的线性范围为0.11 - 3.125 ng/mL,而两种分析物的日内和日间精密度均低于20%。药代动力学特征显示,多次给药后药物暴露量显著降低。a-PD-1的血浆半衰期(22.3小时)比a-PD-L1(46.7小时)略短。据我们所知,这是首次报道的针对这些免疫检查点抑制剂的临床前ELISA,其足够稳健,可用于不同的临床前模型。这些方法有助于了解这些抗体在不同情况下的药代动力学行为及其与反应的关系,从而指导临床环境中最佳剂量的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61ff/7356959/0cf02e51a792/pharmaceutics-12-00595-g001.jpg

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