Charge-Reversal Polymer Nano-modulators for Photodynamic Immunotherapy of Cancer

被引:120
作者
He, Shasha [1 ]
Li, Jingchao [1 ]
Cheng, Penghui [1 ]
Zeng, Ziling [1 ]
Zhang, Chi [1 ]
Duan, Hongwei [1 ]
Pu, Kanyi [1 ]
机构
[1] Nanyang Technol Univ, Sch Chem & Biomed Engn, Sch Phys & Math Sci, 70 Nanyang Dr, Singapore 637457, Singapore
关键词
cancer therapy; charge reversal; immunotherapy; photodynamic therapy; tumor penetration; GROWTH-FACTOR-BETA; NORCANTHARIDIN;
D O I
10.1002/anie.202106392
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanomedicine can regulate the balance between cytotoxic T lymphocytes (CTLs) and suppressive regulatory T lymphocytes (Tregs), which however has been rarely exploited for cancer immunotherapy. We report a charge-reversal polymer nano-modulator (SPDMCN) activated by tumor micro-environment (TME) for photodynamic immunotherapy of cancer. SPDMCN is constructed by conjugating an immunomodulator (demethylcantharidin, DMC) to the side chains of a photodynamic polymer via an acid-liable linker. The negative charge of SPDMCN ensures its high stability in blood circulation and ideal tumor accumulation; exposure to acidic TME reverses its surface charge to positive, enhancing tumor penetration and locally releasing DMC. Upon near-infrared photoirradiation, SPDMCN generates singlet oxygen to ablate tumors and promote maturation of dendritic cells. Released DMC inhibits protein phosphatase 2 (PP2A) activity and decreases Tregs differentiation. Such combinational action induces a sharp increase in CTL/Treg ratio in TME and effectively inhibits both primary and distant tumors in living mice.
引用
收藏
页码:19355 / 19363
页数:9
相关论文
共 51 条
[1]  
[Anonymous], 2019, ANGEW CHEM, V131, P12810
[2]  
[Anonymous], 2020, ANGEW CHEM, V132, P10720
[3]   Phosphatase PP2A is requisite for the function of regulatory T cells [J].
Apostolidis, Sokratis A. ;
Rodriguez-Rodriguez, Noe ;
Suarez-Fueyo, Abel ;
Dioufa, Nikolina ;
Ozcan, Esra ;
Crispin, Jose C. ;
Tsokos, Maria G. ;
Tsokos, George C. .
NATURE IMMUNOLOGY, 2016, 17 (05) :556-+
[4]   In situ sprayed bioresponsive immunotherapeutic gel for post-surgical cancer treatment [J].
Chen, Qian ;
Wang, Chao ;
Zhang, Xudong ;
Chen, Guojun ;
Hu, Quanyin ;
Li, Hongjun ;
Wang, Jinqiang ;
Wen, Di ;
Zhang, Yuqi ;
Lu, Yifei ;
Yang, Guang ;
Jiang, Chen ;
Wang, Jun ;
Dotti, Gianpietro ;
Gu, Zhen .
NATURE NANOTECHNOLOGY, 2019, 14 (01) :89-+
[5]   Photothermal therapy with immune-adjuvant nanoparticles together with checkpoint blockade for effective cancer immunotherapy [J].
Chen, Qian ;
Xu, Ligeng ;
Liang, Chao ;
Wang, Chao ;
Peng, Rui ;
Liu, Zhuang .
NATURE COMMUNICATIONS, 2016, 7
[6]   NIR-light-mediated spatially selective triggering of anti-tumor immunity via upconversion nanoparticle-based immunodevices [J].
Chu, Hongqian ;
Zhao, Jian ;
Mi, Yongsheng ;
Di, Zhenghan ;
Li, Lele .
NATURE COMMUNICATIONS, 2019, 10 (1)
[7]   Dual Drug Backboned Shattering Polymeric Theranostic Nanomedicine for Synergistic Eradication of Patient-Derived Lung Cancer [J].
Cong, Yuwei ;
Xiao, Haihua ;
Xiong, Hejian ;
Wang, Zigui ;
Ding, Jianxun ;
Li, Chan ;
Chen, Xuesi ;
Liang, Xing-Jie ;
Zhou, Dongfang ;
Huang, Yubin .
ADVANCED MATERIALS, 2018, 30 (11)
[8]   mToR signaling and drug development in cancer [J].
Dancey, Janet .
NATURE REVIEWS CLINICAL ONCOLOGY, 2010, 7 (04) :209-219
[9]   Moving towards personalized treatments of immune-related adverse events [J].
Esfahani, Khashayar ;
Elkrief, Arielle ;
Calabrese, Cassandra ;
Lapointe, Rejean ;
Hudson, Marie ;
Routy, Bertrand ;
Miller, Wilson H., Jr. ;
Calabrese, Leonard .
NATURE REVIEWS CLINICAL ONCOLOGY, 2020, 17 (08) :504-515
[10]   Improving cancer immunotherapy through nanotechnology [J].
Goldberg, Michael S. .
NATURE REVIEWS CANCER, 2019, 19 (10) :587-602