清脆的
背景(考古学)
计算生物学
生物
免疫系统
免疫疗法
免疫学
基因组编辑
癌症免疫疗法
遗传学
基因
古生物学
作者
Matthew B. Dong,Kaizhi Tang,Xiaoyu Zhou,Jingjia J. Zhou,Sidi Chen
标识
DOI:10.1016/j.trecan.2021.11.009
摘要
Clustered regularly interspaced short palindromic repeats (CRISPR) screens have recently been extensively utilized for cancer immunotherapy gene discovery. Multiple types of CRISPR screen technologies, including CRISPRko, CRISPRa, and CRISPRi screens are available for different modes of gene identification. CRISPR screens allow identification of targets in both cancer cells and immune cells, such as T cells. In vivo CRISPR screens enable the discovery of genetic and cellular regulators in the tumor microenvironment. Recent advances in immunotherapy have fundamentally changed the landscape of cancer treatment by leveraging the specificity and selectivity of the adaptive immune system to kill cancer cells. These successes have ushered in a new wave of research aimed at understanding immune recognition with the hope of developing newer immunotherapies. The advent of clustered regularly interspaced short palindromic repeats (CRISPR) technologies and advancement of multiomics modalities have greatly accelerated the discovery process. Here, we review the current literature surrounding CRISPR screens within the context of tumor immunology, provide essential components needed to conduct immune-specific CRISPR screens, and present avenues for future research. Recent advances in immunotherapy have fundamentally changed the landscape of cancer treatment by leveraging the specificity and selectivity of the adaptive immune system to kill cancer cells. These successes have ushered in a new wave of research aimed at understanding immune recognition with the hope of developing newer immunotherapies. The advent of clustered regularly interspaced short palindromic repeats (CRISPR) technologies and advancement of multiomics modalities have greatly accelerated the discovery process. Here, we review the current literature surrounding CRISPR screens within the context of tumor immunology, provide essential components needed to conduct immune-specific CRISPR screens, and present avenues for future research.
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