抗体
效应器
抗原
T细胞
化学
跨膜蛋白
细胞培养
细胞
分子生物学
计算生物学
生物测定
生物
受体
免疫学
生物化学
免疫系统
遗传学
作者
A. N. Doronin,Aleksandr Gordeev,A. E. Kozlov,Ya. A. Smirnova,Maria Puchkova,Viktoria M. Ekimova,Yu. I. Basovskiy,V. V. Solovyev
出处
期刊:Biokhimiya
[Springer Nature]
日期:2019-07-01
卷期号:84 (7): 711-719
被引量:5
标识
DOI:10.1134/s0006297919070034
摘要
PD-1/PD-L1-based therapy has been named a revolution in cancer treatment. By the end of 2018, more than 100 anti-PD-1 and anti-PD-L1 antibodies were in various stages of development, and more than 2000 clinical trials with their use have been registered. Characterization of such antibodies requires a bioassay to determine their biological activity. In this study, we developed a cell-based bioassay for analyzing the activity of anti-PD-1 and anti-PD-L1 antibodies. We chose reporter system consisting of two cell lines and compared several approaches for activation of effector cell line based on superantigens, soluble anti-CD3 antibodies, transmembrane anti-CD3 antibodies, chimeric antigenic receptors (CARs) and bispecific T-cell engager antibodies. The bispecific T-cell engager antibodies offer several advantages over the other approaches. We characterized the bioassay and demonstrated its applicability for analyzing the activity of anti-PD-1 and anti-PD-L1 antibodies. The proposed bioassay can be useful in the development of new therapeutic agents and methods for their characterization.
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