化学
癌症免疫疗法
吞噬作用
巨噬细胞
免疫疗法
癌症研究
癌症治疗
纳米颗粒
癌细胞
癌症
癌症治疗
免疫系统
细胞生物学
细胞毒性
生物化学
纳米技术
生物物理学
作者
Tao Zhang,Jia-Qi Luo,Yubin Liu,Hui-Han Yu,Xin Zhang,Zhen-Hao Zhuang,Lang Rao,Jin-Zhi Du
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-03-19
卷期号:26 (12): 4071-4079
标识
DOI:10.1021/acs.nanolett.5c05413
摘要
Macrophages eliminate abnormal cells through phagocytosis, yet their phagocytic ability toward tumor cells is hindered by elevated "don't eat me" signals (e.g., CD47) and insufficient pro-phagocytic signals (e.g., calreticulin, CRT) within the tumor microenvironment. Efficient modulation of macrophage phagocytosis remains a key challenge for immunotherapies. Here, we propose an "AND" logic-gated strategy based on biomimetic nanoparticles to enhance macrophage phagocytosis for improved cancer immunotherapy. The hybrid cell-membrane nanovesicles (Fus-CMVs) were constructed by fusing plasma membranes from engineered 293T cells expressing a high-affinity SIRPα variant to block CD47 (Signal A) with membranes from doxorubicin-pretreated 4T1 tumor cells to display CRT (Signal B). In vitro and in vivo studies demonstrated that the "AND" logic-gated Fus-CMVs significantly increased macrophage engulfment of tumor cells and remarkably inhibited tumor growth in different tumor models when compared with single-signal controls. This approach offers a promising approach to enhance macrophage-mediated antitumor immunotherapy.
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