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用于高效癌症光免疫疗法的肿瘤驻留细胞内细菌清除剂原位激活疫苗

Tumor-Resident Intracellular Bacteria Scavenger Activated In Situ Vaccines for Potent Cancer Photoimmunotherapy.

作者信息

Lv Bai, Zhao Yifan, Li Gang, Jiang Huimei, Zhang Min, Li Zequn, Cao Jie

机构信息

Department of Pharmaceutics, School of Pharmacy, Qingdao University, Qingdao, 266071, China.

Department of Gastrointestinal Surgery, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, 266000, China.

出版信息

Adv Healthc Mater. 2025 Mar;14(7):e2404271. doi: 10.1002/adhm.202404271. Epub 2025 Jan 13.

Abstract

In situ tumor vaccines, which utilize antigens generated during tumor treatment to stimulate a cancer patient's immune system, has become a potential field in cancer immunotherapy. However, due to the immunosuppressive tumor microenvironment (ITME), the generation of tumor antigens is always mild and not sufficient. Tumor-resident intracellular bacteria have been identified as a complete tumor microenvironment component to contribute to creating ITME. Herein, a tumor-resident intracellular bacteria scavenger is designed to induce enhanced antitumor photoimmunotherapy-driven in situ vaccines for treating hypoxic tumors. This scavenger is developed by integrating photosensitizer CyI and antibiotics Doxycycline (Doxy) into thermal-sensitive tumor-derived exosomes fused liposomes (ECDL). In vitro and in vivo results showed that ECDL could homologous target to cancer cells and restrict the respiration of mitochondrial to reduce tumor hypoxia, thus providing continuous oxygen to eliminate both tumor cells and tumor-resident intracellular bacteria, which could induce in situ vaccines for ablating the primary tumor and inhibiting the tumor metastasis and recurrence. Moreover, eliminating tumor-resident intracellular bacteria neutralizes the ITME and triggers the production of bacterial-related neoantigens, which could further strength the immunotherapy. This study provided versatile and effective in situ vaccines that are promising for local, abscopal, and metastatic tumor treatment.

摘要

原位肿瘤疫苗利用肿瘤治疗过程中产生的抗原刺激癌症患者的免疫系统,已成为癌症免疫治疗的一个潜在领域。然而,由于免疫抑制性肿瘤微环境(ITME),肿瘤抗原的产生总是微弱且不足的。肿瘤驻留细胞内细菌已被确定为有助于形成ITME的完整肿瘤微环境成分。在此,设计了一种肿瘤驻留细胞内细菌清除剂,以诱导增强的抗肿瘤光免疫治疗驱动的原位疫苗来治疗缺氧肿瘤。这种清除剂是通过将光敏剂CyI和抗生素强力霉素(Doxy)整合到热敏性肿瘤衍生外泌体融合脂质体(ECDL)中而开发的。体外和体内结果表明,ECDL可以同源靶向癌细胞并限制线粒体呼吸以减少肿瘤缺氧,从而提供持续的氧气以消除肿瘤细胞和肿瘤驻留细胞内细菌,这可以诱导原位疫苗来消融原发性肿瘤并抑制肿瘤转移和复发。此外,消除肿瘤驻留细胞内细菌可中和ITME并触发细菌相关新抗原的产生,这可以进一步增强免疫治疗。这项研究提供了通用且有效的原位疫苗,有望用于局部、远隔效应和转移性肿瘤的治疗。

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