CRISPR-based genetic screens advance cancer immunology

被引:3
作者
Cao, Yuanfang [1 ]
Li, Xueting [1 ]
Pan, Yumu [1 ]
Wang, Huahe [1 ]
Yang, Siyu [1 ]
Hong, Lingjuan [1 ]
Ye, Lupeng [1 ]
机构
[1] Nanjing Univ, Inst Modern Biol, Nanjing 210008, Peoples R China
关键词
gene editing; CRISPR/Cas; genetic screening; cancer immunotherapy; immune cells; HUMAN-CELLS; T-CELLS; TRANSCRIPTIONAL ACTIVATION; ACQUIRED-RESISTANCE; GENOMIC DNA; RNA; TARGET; IMMUNOTHERAPY; ORGANOIDS; KNOCKOUT;
D O I
10.1007/s11427-023-2571-0
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
CRISPR technologies have revolutionized research areas ranging from fundamental science to translational medicine. CRISPR-based genetic screens offer a powerful platform for unbiased screening in various fields, such as cancer immunology. Immune checkpoint blockade (ICB) therapy has been shown to strongly affect cancer treatment. However, the currently available ICBs are limited and do not work in all cancer patients. Pooled CRISPR screens enable the identification of previously unknown immune regulators that can regulate T-cell activation, cytotoxicity, persistence, infiltration into tumors, cytokine secretion, memory formation, T-cell metabolism, and CD4+ T-cell differentiation. These novel targets can be developed as new immunotherapies or used with the current ICBs as new combination therapies that may yield synergistic efficacy. Here, we review the progress made in the development of CRISPR technologies, particularly technological advances in CRISPR screens and their application in novel target identification for immunotherapy.
引用
收藏
页码:2554 / 2562
页数:9
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