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Chimaeric antigen receptor T-cell therapy for tumour immunotherapy
Author(s) -
Huanhuan Sha,
Dandan Wang,
Dali Yan,
Yong Hu,
SuJin Yang,
Si-Wen Liu,
Jifeng Feng
Publication year - 2017
Publication title -
bioscience reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.938
H-Index - 77
eISSN - 1573-4935
pISSN - 0144-8463
DOI - 10.1042/bsr20160332
Subject(s) - chimeric antigen receptor , immunotherapy , cd19 , cell therapy , cancer immunotherapy , antigen , clinical trial , medicine , t cell , immunology , immune system , cancer , cancer research , biology , cell , genetics
Chimaeric antigen receptor (CAR) T-cell therapies, as one of the cancer immunotherapies, have heralded a new era of treating cancer. The accumulating data, especially about CAR-modified T cells against CD19 support that CAR T-cell therapy is a highly effective immune therapy for B-cell malignancies. Apart from CD19, there have been many trials of CAR T cells directed other tumour specific or associated antigens (TSAs/TAAs) in haematologic malignancies and solid tumours. This review will briefly summarize basic CAR structure, parts of reported TSAs/TAAs, results of the clinical trials of CAR T-cell therapies as well as two life-threatening side effects. Experiments in vivo or in vitro, ongoing clinical trials and the outlook for CAR T-cell therapies also be included. Our future efforts will focus on identification of more viable cancer targets and more strategies to make CAR T-cell therapy safer.

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