Challenges and future perspectives for high-throughput chimeric antigen receptor T cell discovery

被引:0
作者
Butler, Savannah E. [1 ]
Ackerman, Margaret E. [1 ,2 ]
机构
[1] Geisel Sch Med Dartmouth, Dept Microbiol & Immunol, Hanover, NH USA
[2] Dartmouth Coll, Thayer Sch Engn, 14 Engn Dr, Hanover, NH 03755 USA
基金
美国国家卫生研究院;
关键词
CYTOKINE SECRETION; DIRECTED EVOLUTION; VARIABLE REGIONS; HUMAN-ANTIBODIES; HIGH-AFFINITY; ON-TARGET; SINGLE; DISPLAY; OPTIMIZATION; ACTIVATION;
D O I
10.1016/j.copbio.2024.103216
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Novel chimeric antigen receptor (CAR) T cell designs are being developed to overcome challenges with tumor recognition, persistence, and immune suppression within the tumor microenvironment. Whereas traditional CAR engineering is an iterative, hypothesis-driven process in which novel designs are rationally constructed and tested for in vivo efficacy, drawing from the fields of small-molecule and protein-based therapeutic discovery, we consider how high-throughput, functional screening technologies are beginning to be applied for the development of promising CAR candidates. We review how the development of high-throughput screening methods has the potential to streamline the CAR discovery process, ultimately improving efficiency and clinical efficacy.
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页数:13
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