Mesothelin CAR-T cells secreting PD-L1 blocking scFv for pancreatic cancer treatment

被引:3
|
作者
Wang, Yeying [1 ,2 ]
Fang, Xiaoyan [1 ]
Li, Minghao [1 ]
Ye, Jing [1 ]
Zhao, Shimin [1 ]
Yu, Lei [1 ]
Wang, Jing [1 ]
Wang, Yiting [1 ]
Yan, Zhiqiang [1 ]
机构
[1] East China Normal Univ, Shanghai Engn Res Ctr Mol Therapeut & New Drug De, Sch Chem & Mol Engn, Inst Biomed Engn & Technol, Shanghai 200062, Peoples R China
[2] Lanzhou Univ, Med Frontier Innovat Res Ctr, Hosp 1, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金;
关键词
CAR-T cells; Mesothelin antigen; PD-L1-blocking antibody; Immunosuppression Pancreatic cancer; IMMUNOTHERAPY;
D O I
10.1016/j.cancergen.2022.10.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PD-1/PD-L1 pathway caused immunosuppression accounts, at least partly, for the poor therapeutic effect of Chimeric Antigen Receptor T (CAR-T) on solid tumors. In this study, we designed and prepared CAR-T cells that could secrete PD-L1 blocking antibody and target Mesothelin antigen (Sec-MesoCAR-T), to remove the immunosuppressive effect of tumor on CAR-T cells, thereby increasing the therapeutic effect of CAR-T cells on pancreatic cancer. The CAR-T cells that could not secret PD-L1 blocking antibodies (MesoCAR-T) were used as a control. Sec-MesoCAR-T cells showed an enhanced inhibitory effect on BxPC3 tumor than MesoCAR-T cells in vitro and in vivo. Besides, Sec-MesoCAR-T cells secreted higher level of cytokines including IL-2, IL-6 and IFN-.in vitro than MesoCAR-T cells. Following injection, there were significantly more CAR-T cells in the peripheral blood of Sec-MesoCAR-T group than that of MesoCAR-T group. This work demonstrated that the PD-L1 antibody secreted by Sec-MesoCAR-T cells relieved the immunosuppressive effect of pancreatic cancer on CAR-T cells and improved the anti-tumor activity of CAR-T cells, which has a good guiding significance for the clinical application of CAR-T cells in treating solid tumors. (c) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:103 / 110
页数:8
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