嵌合抗原受体
自杀基因
免疫疗法
CD19
淋巴瘤
抗原
毒性
免疫学
癌症研究
白血病
临床试验
生物
医学
遗传增强
内科学
生物信息学
免疫系统
基因
生物化学
作者
Shengnan Yu,Ming Yi,Shuang Qin,Kongming Wu
标识
DOI:10.1186/s12943-019-1057-4
摘要
Chimeric antigen receptor T (CAR-T) cell therapy is an emerging and effective cancer immunotherapy. Especially in hematological malignancies, CAR-T cells have achieved exciting results. Two Anti-CD19 CAR-T therapies have been approved for the treatment of CD19-positive leukemia or lymphoma. However, the application of CAR-T cells is obviously hampered by the adverse effects, such as cytokines release syndrome and on-target off-tumor toxicity. In some clinical trials, patients quitted the treatment of CAR-T cells due to life-threatening toxicity. Seeking to alleviate these toxicities or prevent the occurrence, researchers have developed a number of safety strategies of CAR-T cells, including suicide genes, synthetic Notch receptor, on-switch CAR, combinatorial target-antigen recognition, bispecific T cell engager and inhibitory CAR. This review summarized the preclinical studies and clinical trials of the safety strategies of CAR-T cells and their respective strengths and weaknesses.
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