| Literature DB >> 33646061 |
Yijian Li1,2, Qianqian Gao2, Huan Liu2, Shufen Lin2, Huanyi Chen2, Renpeng Ding2, Ying Gu2, Cheng-Chi Chao2, Xuan Dong2,3.
Abstract
The switchable chimeric antigen receptors (CARs) have shown many advantages in CAR T-cell therapy. However, human primary T-cells are required to evaluate antigen-specific adaptors by IFN-γ assay or FACS analysis, which limits the throughput of adaptor screening. A sensitive and robust CD16-CAR Jurkat NFAT-eGFP reporter system has been developed to assess the therapeutic efficacy of antibody-targeted CAR-T-cell by effectively evaluating the T-cell activation by various tumor cells and the impact of immune checkpoint inhibitor antibodies. This reporter system facilitates the screening of targeted antibodies in a high throughput manner for the development of improved T-cell immunotherapy.Entities:
Keywords: CD16-CAR; PD-L1; cetuximab; immunotherapy
Mesh:
Substances:
Year: 2021 PMID: 33646061 DOI: 10.1080/07357907.2021.1894570
Source DB: PubMed Journal: Cancer Invest ISSN: 0735-7907 Impact factor: 2.176