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嵌合抗原受体(CAR)转基因表达的调控以设计半自主CAR-T细胞

Regulation of CAR transgene expression to design semiautonomous CAR-T.

作者信息

Głowacki Paweł, Tręda Cezary, Rieske Piotr

机构信息

Department of Tumor Biology, Chair of Medical Biology, Medical University of Lodz, Zeligowskiego 7/9 Street, 90-752 Lodz, Poland.

Department of Research and Development Personather Ltd, Inwestycyjna 7, 95-050 Konstantynow Lodzki, Poland.

出版信息

Mol Ther Oncol. 2024 Jun 14;32(3):200833. doi: 10.1016/j.omton.2024.200833. eCollection 2024 Sep 19.

Abstract

Effective transgene expression is critical for genetically engineered cell therapy. Therefore, one of CAR-T cell therapy'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 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.

摘要

有效的转基因表达对于基因工程细胞治疗至关重要。因此,无论是在已注册产品还是下一代方法中,嵌合抗原受体T细胞(CAR-T)疗法的一个关键关注领域就是转基因的表达。事实证明,临床产品中使用的各种组成型启动子可能会影响CAR-T细胞的抗肿瘤效果,并影响生产过程。此外,下一代CAR-T开始采用远程控制的诱导型启动子甚至自主表达系统,为启动、增强CAR-T以及提高其安全性开辟了新途径。在本文中,对多种组成型和诱导型启动子进行了分类和梳理,以便能够比较它们的优缺点以及临床应用情况。最后,阐述了基于合成Notch的逻辑门,展示了所需外部信号与基因工程细胞反应的耦合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3533/11344471/8d4fe11a167c/fx1.jpg

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