Enhancing CAR-T cell therapy against solid tumor by drug-free triboelectric immunotherapy

被引:1
|
作者
Li, Haimei [1 ,2 ]
Wang, Zichen [1 ,2 ]
Hu, Yulin [1 ,2 ]
He, Guangqin [1 ,2 ]
Huang, Liang [7 ,8 ]
Liu, Yi [3 ,4 ,6 ]
Wang, Zhong Lin [5 ]
Jiang, Peng [1 ,2 ]
机构
[1] Wuhan Univ, Zhongnan Hosp, Sch Pharmaceut Sci, Dept Orthoped Trauma & Microsurg, Wuhan 430071, Peoples R China
[2] Wuhan Univ, Key Lab Combinatorial Biosynth & Drug Discovery MO, Wuhan 430072, Peoples R China
[3] South Cent Minzu Univ, Sch Chem & Mat Sci, Wuhan 430074, Peoples R China
[4] South Cent Minzu Univ, Sch Pharmaceut Sci, Wuhan 430074, Peoples R China
[5] Chinese Acad Sci, Beijing Inst Nanoenergy & Nanosyst, Beijing 100083, Peoples R China
[6] Hubei Univ Sci & Technol, Sch Nucl Technol & Chem & Biol, Hubei Key Lab Radiat Chem & Funct Mat, Xianning 437100, Peoples R China
[7] Chinese Acad Med Sci & Peking Union Med Coll, State Key Lab Expt Hematol, Inst Hematol & Blood Dis Hosp, Natl Clin Res Ctr Blood Dis,Haihe Lab Cell Ecosyst, Tianjin 300020, Peoples R China
[8] Tianjin Inst Hlth Sci, Tianjin 301600, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
CAR-T cell; Solid tumor treatment; Triboelectric immunotherapy; Immunosuppressive microenvironment; Triboelectric nanogenerator; CANCER;
D O I
10.1016/j.biomaterials.2024.122871
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Chimeric antigen receptor (CAR) T cell therapy is a highly effective immunotherapy for hematological tumors, but its efficacy against most solid tumors remains challenging. Herein, a novel synergistic combination therapy of drug-free triboelectric immunotherapy and CAR-T cell therapy against solid tumor was proposed. A triboelectric nanogenerator (TENG) that can generate pulsed direct-current by coupling triboelectrification effect and electrostatic breakdown effect was fabricated. The TENG can generate up to 30 pulse direct-current peaks with peak current output approximate to 35 mu A in a single sliding to power the triboelectric immunotherapy. The pulsed direct-current stimulation induced immunogenic cell death of tumor cells (survival rate of 35.9 %), which promoted dendritic cells maturation, accelerated the process of antigen presentation to CAR-T cells and enhanced the systemic adaptive immune response. Furthermore, triboelectric immunotherapy promoted M1-like macrophage polarization, reduced regulatory T cells differentiation and reprogrammed the tumor immunosuppressive microenvironment, which ultimately enhanced the efficacy of CAR-T cells to eradicate nearly 60 % of NALM6 solid tumor mass. Notably, considering that triboelectric immunotherapy is a safe and effective drug-free antitumor strategy, the combined therapy did not increase the burden of double-medication on patients.
引用
收藏
页数:10
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