Designer T-cells and T-cell receptors for customized cancer immunotherapies

被引:5
|
作者
Legut, Mateusz [1 ]
Sewell, Andrew K. [1 ]
机构
[1] Cardiff Univ, Univ Wales Hosp, Sch Med, Div Infect & Immun, Henry Wellcome Bldg, Cardiff CF14 4XN, S Glam, Wales
基金
英国惠康基金;
关键词
BINDING-AFFINITY; PERIPHERAL-BLOOD; ANTIGEN RECEPTOR; GENE-THERAPY; IDENTIFICATION; LYMPHOCYTES; REGRESSION; GENERATION; REACTIVITY; TOXICITY;
D O I
10.1016/j.coph.2018.05.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cancer immunotherapy, focused on harnessing and empowering the immune system against tumours, has transformed modern oncology. One of the most promising avenues in development involves using genetically engineered T-cells to target cancer antigens via specific T-cell receptors (TCRs). TCRs have a naturally low affinity towards cancer associated antigens, and therefore show scope for improvement. Here we describe approaches to procure TCRs with enhanced affinity and specificity towards cancer, using protein engineering or selection of natural TCRs from unadulterated repertoires. In particular, we discuss novel methods facilitating the targeting of tumour-specific mutations. Finally, we provide a prospective outlook on the potential development of novel, off-the-shelf immunotherapies by leveraging recent advances in genome editing.
引用
收藏
页码:96 / 103
页数:8
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