嵌合抗原受体
胆道癌
医学
CD28
癌症研究
抗原
T细胞
癌症
胆道
细胞疗法
内科学
肿瘤科
细胞
受体
免疫疗法
免疫系统
癌细胞
融合蛋白
肿瘤细胞
体外
免疫学
胃肠病学
T细胞受体
抗体
作者
Xueshuai Wan,Jie Zhao,Xiaobo Yang,Xiaowen Mou,Bing Liu,Bin Gao,Weiyue Gu,Haitao Zhao
标识
DOI:10.1016/j.xcrm.2025.102349
摘要
T cell therapy for tumors faces barriers like heterogeneous antigen expression, an unfriendly tumor microenvironment, and limited T cell expansion. We adopt a 3-in-1 strategy to produce super circulating TIL-like (tumor-infiltrating lymphocyte-like) cells (ScTILs): modifying PD-1-positive peripheral blood T cells with an enhance receptor (ER), a PD-1 and CD28 fusion protein to reverse inhibitory signal, and an anti-CD19 chimeric antigen receptor (CAR) for expansion (CFE). ScTILs kill tumor cells effectively in vitro and in vivo. Clinically, ten advanced biliary tract cancer (BTC) patients receive ScTILs treatment; post hoc analysis shows that ScTILs monotherapy yields a median overall survival (OS) of 18.3 months in appropriate dose or normal B cell groups (5/10), outperforming first-line BTC treatment (OS ∼12 months). It skips chemo-pre-treatment and interleukin-2 (IL-2), with better safety, no reliance on surgical materials, and a shorter production cycle. Overall, ScTILs are a promising therapy for future BTC treatment. This study is registered with ChiCTR (ChiCTR2000029738).
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