细胞毒性T细胞
癌症研究
重编程
免疫抑制
免疫系统
体内
医学
免疫疗法
免疫原性
癌症
癌细胞
免疫学
癌症疫苗
抗原呈递
抗原
癌症免疫疗法
细胞毒性
CTL公司*
生物
离体
嵌合抗原受体
抗原提呈细胞
免疫原性细胞死亡
免疫
T细胞
获得性免疫系统
原发性肿瘤
作者
Yuan Gu,Pei Xu,Yanxian Wu,Mengfei Tan,Yan Xu,L. Zhang,Yangyun Wang,Yangyun Wang,Yong Wang,Yong Wang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-02-16
卷期号:20 (8): 6783-6797
标识
DOI:10.1021/acsnano.5c16193
摘要
(BL21) loaded into autologous tumor cells (BL21@Tc) under anaerobic conditions. This system exploits tumor-targeting membrane fusion to deliver BL21 selectively to postoperative residual tumor cells. Activation of intracellular BL21 disrupts cholesterol metabolism, triggering the in vivo reprogramming of tumor cells into a type 1 conventional dendritic cell. These antigen-presenting cell-like tumor cells exhibit enhanced antigen presentation and robustly activate tumor-specific cytotoxic T lymphocytes, effectively remodeling the immunosuppressive postoperative microenvironment. In murine postoperative cancer models, BL21@Tc elicited potent and durable systemic antitumor immunity, significantly inhibiting tumor recurrence and metastasis. Furthermore, BL21@Tc synergized with radiotherapy to improve therapeutic outcomes. This study establishes an innovative anaerobic probiotic-driven platform for in situ antigen-presenting cell reprogramming, offering a powerful strategy for next-generation cancer vaccines targeting postoperative immunosuppression and residual disease.
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