Guan Meng, Xie Xiao-Ting, Zhou Dong, Cheng Kai, Zhang Bin, Xu Xin-Yue, Li Yong, Zhou Yi-Tong, Peng Wei, Chen Li-Li, Dong Peng-Shuo, Chen Si, Zou Jia-Hua, Liu Bo, Zhao Yuan-Di, Fan Jin-Xuan
Britton Chance Center for Biomedical Photonics at Wuhan National Laboratory for Optoelectronics - Hubei Bioinformatics & Molecular Imaging Key Laboratory, Department of Biomedical Engineering, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, Hubei, 430074, P. R. China.
Department of Oncology, Huanggang Central Hospital of Yangtze University, Huanggang, Hubei, 438000, P. R. China.
Adv Sci (Weinh). 2025 Jul;12(27):e2505000. doi: 10.1002/advs.202505000. Epub 2025 Apr 27.
In clinical practice, surgical removal of tumors often leaves behind small tumors and circulating tumor cells, increasing the risk of metastasis and recurrence, which seriously affects treatment outcomes. Immunotherapy activates the immune system to monitor and inhibit tumor metastasis and recurrence long-term. However, inflammatory microenvironments at surgical sites lead to immunosuppressive tumor-associated macrophages (TAMs), causing immune evasion. Additionally, tumor cells overexpress the immune checkpoint CD47, further weakening the phagocytic and cytotoxic functions of macrophages. Here, the bacterial outer membrane vesicles (OMV) hitchhiking on neutrophils are utilized to precisely deliver immune checkpoint blockade antibodies to the tumor resection site. Escherichia coli is reprogrammed to express CD47 antibody and used to extract CD47 antibody-containing OMV, followed by insertion of Ce6 photosensitizer into the membrane (OC47-Ce6). Purified autologous neutrophils phagocytose and carry OC47-Ce6 for precise targeting to the postoperative tumor resection site, mediating tumor cell killing, aCD47 release, and tumor-associated antigen presentation by light. In vitro and in vivo experiments demonstrate that OC47-Ce6 enhances TAM phagocytic function through TAM polarization and CD47 blockade. This approach effectively activates T-cell anti-tumor immune responses and significantly reduces the risk of postoperative tumor recurrence and metastasis.
在临床实践中,手术切除肿瘤后往往会残留小肿瘤和循环肿瘤细胞,增加转移和复发风险,严重影响治疗效果。免疫疗法可激活免疫系统,长期监测并抑制肿瘤转移和复发。然而,手术部位的炎性微环境会导致免疫抑制性肿瘤相关巨噬细胞(TAM)产生,引发免疫逃逸。此外,肿瘤细胞过度表达免疫检查点CD47,进一步削弱巨噬细胞的吞噬和细胞毒性功能。在此,利用搭乘中性粒细胞的细菌外膜囊泡(OMV)将免疫检查点阻断抗体精确递送至肿瘤切除部位。对大肠杆菌进行重编程使其表达CD47抗体,并用于提取含CD47抗体的OMV,随后将Ce6光敏剂插入膜中(OC47-Ce6)。纯化的自体中性粒细胞吞噬并携带OC47-Ce6,精确靶向术后肿瘤切除部位,通过光照介导肿瘤细胞杀伤、aCD47释放以及肿瘤相关抗原呈递。体外和体内实验表明,OC47-Ce6通过TAM极化和CD47阻断增强TAM吞噬功能。该方法有效激活T细胞抗肿瘤免疫反应,并显著降低术后肿瘤复发和转移风险。