A Tumor Environment-Activated Photosensitized Biomimetic Nanoplatform for Precise Photodynamic Immunotherapy of Colon Cancer

被引:11
作者
Xiong, Mengmeng [1 ]
Zhang, Ying [2 ]
Zhang, Huan [1 ]
Shao, Qiaoqiao [3 ]
Hu, Qifan [4 ]
Ma, Junjie [1 ]
Wan, Yiqun [1 ]
Guo, Lan [1 ]
Wan, Xin [1 ]
Sun, Haitao [3 ]
Yuan, Zhongyi [1 ]
Wan, Hao [2 ]
机构
[1] Nanchang Univ, Sch Chem & Chem Engn, Nanchang 330031, Peoples R China
[2] Nanchang Univ, State Key Lab Food Sci & Resources, Nanchang 330047, Peoples R China
[3] East China Normal Univ, Sch Phys & Elect Sci, State Key Lab Precis Spect, Shanghai 200241, Peoples R China
[4] Nanchang Univ, Affiliated Hosp 1, Jiangxi Med Coll, Postdoctoral Innovat Practice Base, Nanchang 330006, Peoples R China
基金
中国国家自然科学基金;
关键词
anti-tumor immune response; biomimetic nanoplatform; evasion of immune surveillance; tumor environment-activated photodynamic therapy; tumor targeting; THERAPY; NANOPARTICLES; EFFICIENT; DELIVERY; PROBE;
D O I
10.1002/advs.202402465
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Aggressive nature of colon cancer and current imprecise therapeutic scenarios simulate the development of precise and effective treatment strategies. To achieve this, a tumor environment-activated photosensitized biomimetic nanoplatform (PEG2000-SiNcTI-Ph/CpG-ZIF-8@CM) is fabricated by encapsulating metal-organic framework loaded with developed photosensitizer PEG2000-SiNcTI-Ph and immunoadjuvant CpG oligodeoxynucleotide within fusion cell membrane expressing programmed death protein 1 (PD-1) and cluster of differentiation 47 (CD47). By stumbling across, systematic evaluation, and deciphering with quantum chemical calculations, a unique attribute of tumor environment (low pH plus high concentrations of adenosine 5 '-triphosphate (ATP))-activated photodynamic effect sensitized by long-wavelength photons is validated for PEG2000-SiNcTI-Ph/CpG-ZIF-8@CM, advancing the precision of cancer therapy. Moreover, PEG2000-SiNcTI-Ph/CpG-ZIF-8@CM evades immune surveillance to target CT26 colon tumors in mice mediated by CD47/signal regulatory proteins alpha (SIRP alpha) interaction and PD-1/programmed death ligand 1 (PD-L1) interaction, respectively. Tumor environment-activated photodynamic therapy realized by PEG2000-SiNcTI-Ph/CpG-ZIF-8@CM induces immunogenic cell death (ICD) to elicit anti-tumor immune response, which is empowered by enhanced dendritic cells (DC) uptake of CpG and PD-L1 blockade contributed by the nanoplatform. The photodynamic immunotherapy efficiently combats primary and distant CT26 tumors, and additionally generates immune memory to inhibit tumor recurrence and metastasis. The nanoplatform developed here provides insights for the development of precise cancer therapeutic strategies. A photosensitized biomimetic nanoplatform (PEG2000-SiNcTI-Ph/CpG-ZIF-8@CM) activated by tumor environment is designed for precise therapy of colon cancer. The ability of developed molecular photosensitizer PEG2000-SiNcTI-Ph to generate ROS sensitized by long-wavelength photons is dormant after being loaded into ZIF-8. Responding to tumor environment (low pH plus high ATP concentrations), PEG2000-SiNcTI-Ph/CpG-ZIF-8@CM is degraded to restore ROS generating capacity sensitized by long-wavelength photons. image
引用
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页数:17
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