A biomimetic spore nanoplatform for boosting chemodynamic therapy and bacteria-mediated antitumor immunity for synergistic cancer treatment

被引:0
|
作者
Zheng, Cuixia [2 ]
Sun, Lingling [5 ]
Zhao, Hongjuan [1 ,3 ]
Niu, Mengya [1 ]
Zhang, Dandan [1 ]
Liu, Xinxin [1 ]
Song, Qingling [1 ]
Zhong, Weijie [2 ]
Wang, Baojin [4 ]
Zhang, Yun [1 ,3 ]
Wang, Lei [1 ,3 ]
机构
[1] Zhengzhou Univ, Sch Pharmaceut Sci, Zhengzhou 450001, Peoples R China
[2] Henan Univ, Huaihe Hosp, Translat Med Ctr, Kaifeng 475000, Peoples R China
[3] Henan Normal Univ, Pingyuan Lab, Xinxiang 453007, Peoples R China
[4] Zhengzhou Univ, Affiliated Hosp 3, Gynecol, Zhengzhou 450052, Peoples R China
[5] Shandong Univ, Weihai Municipal Hosp, Cheeloo Coll Med, Weihai 264200, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Biomimetic spore shell; Bacteria-mediated antitumor; therapy; Chemodynamic therapy; Immunotherapy; Tumor microenvironment; DOXORUBICIN; PYROPTOSIS; DELIVERY;
D O I
10.1016/j.ajps.2024.100912
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Bacterial -based antitumor immunity has become a promising strategy to activate the immune system for fighting cancer. However, the potential application of bacterial therapy is hindered by the presence of instability and susceptibility to infections within bacterial populations. Furthermore, monotherapy is ineffective in completely eliminating complex cancer with multiple contributing factors. In this study, based on our discovery that spore shell (SS) of Bacillus coagulans exhibits excellent tumor -targeting ability and adjuvant activity, we develop a biomimetic spore nanoplatform to boost bacteria -mediated antitumor therapy, chemodynamic therapy and antitumor immunity for synergistic cancer treatment. In detail, SS is separated from probiotic spores and then attached to the surface of liposome (Lipo) that was loaded with hemoglobin (Hb), glucose oxidase (GOx) and JQ1 to construct SS@Lipo/Hb/GOx/JQ1. In tumor tissue, highly toxic hydroxyl radicals ( center dot OH) are generated via sequential catalytic reactions: GOx catalyzing glucose into H 2 O 2 and Fe 2 + in Hb decomposing H 2 O 2 into center dot OH. The combination of center dot OH and SS adjuvant can improve tumor immunogenicity and activate immune system. Meanwhile, JQ1-mediated down -regulation of PD -L1 and Hb-induced hypoxia alleviation synergistically reshape immunosuppressive tumor microenvironment and potentiate immune response. In this manner, SS@Lipo/Hb/GOx/JQ1 significantly suppresses tumor growth and metastasis. To summarize, the nanoplatform represents an optimum strategy to potentiate bacteria -based cancer immunotherapy. (c) 2024 Shenyang Pharmaceutical University. Published by Elsevier B.V. This is an open access article under the CC BY -NC -ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )
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页数:13
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