Regulation of CAR transgene expression to design semiautonomous CAR-T

被引:0
|
作者
Glowacki, Pawel [1 ]
Treda, Cezary [1 ,2 ]
Rieske, Piotr [1 ,2 ]
机构
[1] Med Univ Lodz, Chair Med Biol, Dept Tumor Biol, Zeligowskiego 7-9 St, PL-90752 Lodz, Poland
[2] Dept Res & Dev Personather Ltd, Inwestycyjna 7, PL-95050 Konstantynow Lodzki, Poland
来源
MOLECULAR THERAPY ONCOLOGY | 2024年 / 32卷 / 03期
关键词
ANTIGEN RECEPTOR EXPRESSION; GENE-EXPRESSION; TRANSCRIPTION FACTORS; INDUCIBLE SYSTEM; HISTONE H3; ON SYSTEM; IN-VIVO; CELLS; PROMOTER; ACTIVATION;
D O I
10.1016/j.omton.2024.200833
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Effective transgene expression is critical for genetically engineered cell therapy. Therefore, one of CAR-T cell therapy's ' s critical areas of interest, both in registered products and next-generation approaches is the expression of transgenes. It turns out that various constitutive promoters used in clinical products may influence fl uence CAR-T cell antitumor effectiveness and impact the manufacturing process. Furthermore, next-generation CAR-T starts to install remotely controlled inducible promoters or even autonomous expression systems, opening new ways of priming, boosting, and increasing the safety of CAR-T. In this article, a wide range of constitutive and inducible promoters has been grouped and structured, making it possible to compare their pros and cons as well as clinical usage. Finally, logic gates based on Synthetic Notch have been elaborated, demonstrating the coupling of desired external signals with genetically engineered cellular responses.
引用
收藏
页数:19
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