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通过利用内源性干扰素-γ启动子来表达细胞因子构建一种新型TRUCK。

Building a novel TRUCK by harnessing the endogenous IFN-gamma promoter for cytokine expression.

作者信息

Ma Liya, Zhang Kaiwen, Xu Jian, Wang Jian, Jiang Ting, Du Xiaolong, Zhang Jiaxin, Huang Jing, Ren Fengyi, Liu Dong, Xue Weiwei, Kan Dongxu, Yao Mengjiao, Liang Yutian, Jason-Sun Hongxing

机构信息

Shenzhen Celconta Life Science Co. Ltd., Shenzhen, Guangdong, China.

Shenzhen Celconta Life Science Co. Ltd., Shenzhen, Guangdong, China.

出版信息

Mol Ther. 2024 Aug 7;32(8):2728-2740. doi: 10.1016/j.ymthe.2024.06.017. Epub 2024 Jun 15.

Abstract

Despite the remarkable success of chimeric antigen receptor (CAR) T therapy in hematological malignancies, its efficacy in solid tumors remains limited. Cytokine-engineered CAR T cells offer a promising avenue, yet their clinical translation is hindered by the risks associated with constitutive cytokine expression. In this proof-of-concept study, we leverage the endogenous interferon (IFN)-γ promoter for transgenic interleukin (IL)-15 expression. We demonstrate that IFN-γ expression is tightly regulated by T cell receptor signaling. By introducing an internal ribosome entry site IL15 into the 3' UTR of the IFN-γ gene via homology directed repair-mediated knock-in, we confirm that IL-15 expression can co-express with IFN-γ in an antigen stimulation-dependent manner. Importantly, the insertion of transgenes does not compromise endogenous IFN-γ expression. In vitro and in vivo data demonstrate that IL-15 driven by the IFN-γ promoter dramatically improves CAR T cells' antitumor activity, suggesting the effectiveness of IL-15 expression. Last, as a part of our efforts toward clinical translation, we have developed an innovative two-gene knock-in approach. This approach enables the simultaneous integration of CAR and IL-15 genes into TRAC and IFN-γ gene loci using a single AAV vector. CAR T cells engineered to express IL-15 using this approach demonstrate enhanced antitumor efficacy. Overall, our study underscores the feasibility of utilizing endogenous promoters for transgenic cytokines expression in CAR T cells.

摘要

尽管嵌合抗原受体(CAR)T细胞疗法在血液系统恶性肿瘤中取得了显著成功,但其在实体瘤中的疗效仍然有限。细胞因子工程化的CAR T细胞提供了一条有前景的途径,然而其临床转化受到与组成型细胞因子表达相关风险的阻碍。在这项概念验证研究中,我们利用内源性干扰素(IFN)-γ启动子进行转基因白细胞介素(IL)-15表达。我们证明IFN-γ表达受T细胞受体信号严格调控。通过同源定向修复介导的敲入将内部核糖体进入位点IL15引入IFN-γ基因的3'非翻译区,我们证实IL-15表达可以以抗原刺激依赖的方式与IFN-γ共表达。重要的是,转基因的插入不会损害内源性IFN-γ表达。体外和体内数据表明,由IFN-γ启动子驱动的IL-15显著提高了CAR T细胞的抗肿瘤活性,表明IL-15表达的有效性。最后,作为我们临床转化努力的一部分,我们开发了一种创新的双基因敲入方法。这种方法能够使用单个腺相关病毒(AAV)载体将CAR和IL-15基因同时整合到TRAC和IFN-γ基因座。使用这种方法工程化表达IL-15的CAR T细胞表现出增强的抗肿瘤功效。总体而言,我们的研究强调了利用内源性启动子在CAR T细胞中进行转基因细胞因子表达的可行性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc53/11405158/888ac9525e98/fx1.jpg

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