Jurkat细胞
NFAT公司
单克隆抗体
抗体
嵌合抗原受体
抗原
分子生物学
T细胞
生物
癌症研究
化学
免疫学
免疫系统
遗传学
转录因子
基因
作者
Diana Darowski,Christian Jöst,Kay Stubenrauch,Uwe Wessels,Jörg Benz,A. Ehler,Anne Freimoser–Grundschober,Peter Brünker,Ekkehard Mössner,Pablo Umaña,Sebastian Kobold,Christian Klein
标识
DOI:10.1093/protein/gzz027
摘要
Monoclonal antibody-based therapeutics are an integral part of treatment of different human diseases, and the selection of suitable antibody candidates during the discovery phase is essential. Here, we describe a novel, cellular screening approach for the identification and characterization of therapeutic antibodies suitable for conversion into T cell bispecific antibodies using chimeric antigen receptor (CAR) transduced Jurkat-NFAT-luciferase reporter cells (CAR-J). For that purpose, we equipped a Jurkat-NFAT reporter cell line with a universal CAR, based on a monoclonal antibody recognizing the P329G mutation in the Fc-part of effector-silenced human IgG1-antibodies. In addition to scFv-based second generation CARs, Fab-based CARs employing the P329G-binder were generated. Using these anti-P329G-CAR-J cells together with the respective P329G-mutated IgG1-antibodies, we established a system, which facilitates the rapid testing of therapeutic antibody candidates in a flexible, high throughput setting during early stage discovery. We show that both, scFv- and Fab-based anti-P329G-CAR-J cells elicit a robust and dose-dependent luciferase signal if the respective antibody acts as an adaptor between tumor target and P329G-CAR-J cells. Importantly, we could demonstrate that functional characteristics of the antibody candidates, derived from the anti-P329G-CAR-J screening assay, are predictive for the functionality of these antibodies in the T cell bispecific antibody format.
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