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Immunological Synapse Predicts Effectiveness of Chimeric Antigen Receptor Cells.


ABSTRACT: Chimeric antigen receptor (CAR)-modified T cell therapy has the potential to improve the overall survival of patients with malignancies by enhancing the effectiveness of CAR T cells. Precisely predicting the effectiveness of various CAR T cells represents one of today's key unsolved problems in immunotherapy. Here, we predict the effectiveness of CAR-modified cells by evaluating the quality of the CAR-mediated immunological synapse (IS) by quantitation of F-actin, clustering of tumor antigen, polarization of lytic granules (LGs), and distribution of key signaling molecules within the IS. Long-term killing capability, but not secretion of conventional cytokines or standard 4-hr cytotoxicity, correlates positively with the quality of the IS in two different CAR T cells that share identical antigen specificity. Xenograft model data confirm that the quality of the IS in vitro correlates positively with performance of CAR-modified immune cells in vivo. Therefore, we propose that the quality of the IS predicts the effectiveness of CAR-modified immune cells, which provides a novel strategy to guide CAR therapy.

SUBMITTER: Xiong W 

PROVIDER: S-EPMC6080133 | biostudies-literature | 2018 Apr

REPOSITORIES: biostudies-literature

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Immunological Synapse Predicts Effectiveness of Chimeric Antigen Receptor Cells.

Xiong Wei W   Chen Yuhui Y   Kang Xi X   Chen Zhiying Z   Zheng Peilin P   Hsu Yi-Hsin YH   Jang Joon Hee JH   Qin Lidong L   Liu Hao H   Dotti Gianpietro G   Liu Dongfang D  

Molecular therapy : the journal of the American Society of Gene Therapy 20180302 4


Chimeric antigen receptor (CAR)-modified T cell therapy has the potential to improve the overall survival of patients with malignancies by enhancing the effectiveness of CAR T cells. Precisely predicting the effectiveness of various CAR T cells represents one of today's key unsolved problems in immunotherapy. Here, we predict the effectiveness of CAR-modified cells by evaluating the quality of the CAR-mediated immunological synapse (IS) by quantitation of F-actin, clustering of tumor antigen, po  ...[more]

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