Arming CAR-T cells with cytokines and more: Innovations in the fourth-generation CAR-T development

被引:34
|
作者
Tang, Lin [1 ,2 ]
Pan, Sheng [1 ,2 ]
Wei, Xuyong [2 ]
Xu, Xiao [1 ,2 ]
Wei, Qiang [1 ,2 ]
机构
[1] Zhejiang Univ, Sch Med, Hangzhou 310058, Peoples R China
[2] Zhejiang Univ, Key Lab Integrated Oncol & Intelligent Med Zhejian, Dept Hepatobiliary & Pancreat Surg, Affiliated Hangzhou Peoples Hosp 1,Sch Med, Hangzhou 310006, Peoples R China
基金
中国国家自然科学基金;
关键词
ANTITUMOR-ACTIVITY; SELECTIVE EXPANSION; ANTIBODY THERAPY; DENDRITIC CELLS; CO-STIMULATION; RECEPTOR; LYMPHOCYTES; GENE; ACTIVATION; EXHAUSTION;
D O I
10.1016/j.ymthe.2023.09.021
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Chimeric antigen receptor T cells (CAR-T) therapy has shown great potential in tumor treatment. However, many factors impair the efficacy of CAR-T therapy, such as antigenic heterogeneity and loss, limited potency and persistence, poor infiltration capacity, and a suppressive tumor microenvironment. To overcome these obstacles, recent studies have reported a new generation of CAR-T cells expressing cytokines called armored CAR-T, TRUCK-T, or the fourth-generation CAR-T. Here we summarize the strategies of arming CAR-T cells with natural or synthetic cytokine signals to enhance their anti-tumor capacity. Moreover, we summarize the advances in CAR-T cells expressing non-cytokine proteins, such as membrane receptors, antibodies, enzymes, co-stimulatory molecules, and transcriptional factors. Furthermore, we discuss several prospective strategies for armored CAR-T therapy development. Altogether, these ideas may provide new insights for the innovations of the next-generation CAR-T therapy.
引用
收藏
页码:3146 / 3162
页数:17
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