刺
医学
免疫疗法
干扰素
嵌合抗原受体
基因
干扰素基因刺激剂
癌症研究
胰腺癌
癌症免疫疗法
T细胞
抗原
干扰素
细胞
癌症
免疫学
遗传增强
胰腺
细胞因子
融合基因
免疫系统
作者
Ignazio Piseddu,Rebekka Endres,Fabian Lanzl,Linda Hammann,Marleen Bérouti,Matthias Thaler,Lisa Fahr,Hannah Fischer,Varvara Varlamova,Jan Gärtig,Daniel Nixdorf,Patrick Layritz,Charlotte Marx,Christine Hörth,Catharina Witte,Alpay Bulut,David Illig,Anne Marie Senz,Lesca Holdt,Ivonne Regel
标识
DOI:10.1053/j.gastro.2026.01.031
摘要
BACKGROUND & AIMS: Chimeric antigen receptor (CAR) T cells have shown great potential in hematological cancers, but lack efficacy in solid tumors, highlighting the need for novel strategies. Stimulator of interferon genes (STING) activation was shown to inflame the tumor microenvironment, but combination of STING agonists and CAR-T cells might be limited by detrimental outcomes of T cell-intrinsic STING activation. In this study, we evaluated the potential of combining STING agonists and CAR-T cells in the context of pancreatic cancer. METHODS: We assessed the synergy of CRISPR-Cas9-edited CAR-T cells and the STING agonist diABZI within a T cell exhaustion model in vitro and both xenograft and syngeneic mouse models in vivo. RESULTS: Combination of STING-ablated CAR-T cells and diABZI resulted in enhanced cancer cell killing, increased CAR-T cell proliferation, reduced exhaustion, and expansion of an effector-memory phenotype in vitro. Mechanistically, superior CAR-T cell functionality required genetic ablation of STING in CAR-T cells and was dependent on cancer cell-intrinsic STING signaling on STING-agonistic treatment. Moreover, we identified a synergistic feedback loop comprising the T cell-secreted cytokines interferon-γ and tumor necrosis factor, which prime STING signaling within cancer cells, thereby potentiating the outcomes of cancer cell-intrinsic STING activation in inducing ameliorated CAR-T cell states. Ultimately, we could demonstrate that combination of STING deficient CAR-T cells and diABZI was able to provide enhanced tumor control in both xenograft and syngeneic mouse models. This was accompanied by increased intratumoral CAR-T cell numbers and reprogramming of the tumor microenvironment in vivo. CONCLUSIONS: Our findings suggest that STING deficient CAR-T cells stand to benefit from STING agonists to improve CAR-T cell therapy for immune-deprived cancers such as pancreatic cancer.
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