Therapeutic T cells with 3-in-1 strategy for the treatment of biliary tract cancer

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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Publication Details

Journal
Cell Reports Medicine
Published
2025-09-23
DOI
https://doi.org/10.1016/j.xcrm.2025.102349
Citations
1
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
1.05
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article

Therapeutic T cells with 3-in-1 strategy for the treatment of biliary tract cancer

Xueshuai Wan, Jie Zhao, Weiyue Gu, Bing Liu et al.
1 citations
Cell Reports Medicine
CAR-T cell therapy research
1.05
article

Therapeutic T cells with 3-in-1 strategy for the treatment of biliary tract cancer

Xueshuai Wan, Jie Zhao, Weiyue Gu, Bing Liu, Haitao Zhao, Bin Gao, Xiaobo Yang, Xiaowen Mou
article en
1 citations

Abstract

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).

Cell Reports MedicineVol. 6(10)
Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Peking Union Medical College Hospital (CN), Cell Technology (China) (HK), Shine Micro (United States) (US)
Openalex Percentile: Top 18%
CAR-T cell therapy research
1.05
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Therapeutic T cells with 3-in-1 strategy for the treatment of biliary tract cancer — Xueshuai Wan, Jie Zhao, et al. · Cell Reports Medicine (2025) | TGRS Research Map | TGRS