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Biochemistry (Mosc) ; 84(7): 711-719, 2019 Jul.
Article in English | MEDLINE | ID: mdl-31509723

ABSTRACT

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.


Subject(s)
Antibodies, Monoclonal/immunology , B7-H1 Antigen/immunology , Biological Assay/methods , Luminescent Measurements/methods , Programmed Cell Death 1 Receptor/immunology , T-Lymphocytes/immunology , Antibodies, Bispecific , Antigens, Surface/immunology , B7-H1 Antigen/antagonists & inhibitors , CD3 Complex/metabolism , Genes, Reporter , Genetic Vectors , Humans , Jurkat Cells , Lymphocyte Activation , NFATC Transcription Factors/metabolism , Programmed Cell Death 1 Receptor/antagonists & inhibitors , Receptors, Chimeric Antigen/genetics
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