Immunologically modified MnFe2O4 nanoparticles to synergize photothermal therapy and immunotherapy for cancer treatment

被引:71
作者
Zhou, Benqing [1 ,2 ]
Wu, Qiang [1 ]
Wang, Meng [1 ]
Hoover, Ashley [3 ]
Wang, Xin [1 ]
Zhou, Feifan [1 ]
Towner, Rheal A. [4 ]
Smith, Nataliya [4 ]
Saunders, Debra [4 ]
Song, Jun [1 ]
Qu, Junle [1 ]
Chen, Wei R. [3 ]
机构
[1] Shenzhen Univ, Coll Phys & Optoelect Engn, Key Lab Optoelect Devices & Syst, Minist Educ & Guangdong Prov, Shenzhen 518060, Peoples R China
[2] Shantou Univ, Dept Biomed Engn, Coll Engn, Shantou 515063, Peoples R China
[3] Univ Cent Oklahoma, Coll Math & Sci, Ctr Interdisciplinary Biomed Educ & Res, Biophoton Res Lab, Edmond, OK 73034 USA
[4] Oklahoma Med Res Fdn, Adv Magnet Resonance Ctr, 825 NE 13th St, Oklahoma City, OK 73104 USA
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
MnFe2O4; nanoparticles; Photothermal therapy; Immunotherapy; Immunoadjuvant; OVA; CHECKPOINT BLOCKADE; T-CELLS; PHOTODYNAMIC THERAPY; DELIVERY; VACCINE; COMBINATION; GROWTH;
D O I
10.1016/j.cej.2020.125239
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Immunotherapy has been a promising candidate for cancer treatment. The combination of photothermal therapy (PTT) and immunotherapy have shown to cause tumor ablation and induce host immune response. However, this strategy is often hampered by a limited immune response and undesirable immunosuppression. In this work, we developed an immunologically modified nanoplatform, using ovalbumin (OVA)-coated PEGylated MnFe2O4 nanoparticles (NPs) loaded with R837 immunoadjuvant (R837-OVA-PEG-MnFe2O4 NPs) to synergize PTT and immunotherapy for the treatment of breast cancer. The designed R837-OVA-PEG-MnFe2O4 NPs are able to elicit significant immune responses in vitro and in vivo. MnFe2O4 NPs also allowed for a reduction of systemic immunosuppression through downregulation of M2-associated cytokines. More importantly, the R837-OVA-PEGMnFe(2)O(4) NPs under laser irradiation effectively inhibited tumor growth and prevented lung metastases, leading to a prolonged survival time and improved survival rate. In addition, the designed multitasking MnFe2O4 NPs showed as a desirable contrast agent for magnetic resonance (MR) imaging to diagnose orthotopic breast tumor in vivo. Our work provides a novel strategy for combined PTT and improved immunotherapy in the treatment of breast and other metastatic cancers.
引用
收藏
页数:12
相关论文
共 51 条
  • [1] In vivo Expansion, Persistence, and Function of Peptide Vaccine-Induced CD8 T Cells Occur Independently of CD4 T Cells
    Assudani, Deepak
    Cho, Hyun-Il
    DeVito, Nicholas
    Bradley, Norma
    Celis, Esteban
    [J]. CANCER RESEARCH, 2008, 68 (23) : 9892 - 9899
  • [2] Nutlin-3a and Cytokine Co-loaded Spermine-Modified Acetalated Dextran Nanoparticles for Cancer Chemo-Immunotherapy
    Bauleth-Ramos, Tomas
    Shahbazi, Mohammad-Ali
    Liu, Dongfei
    Fontana, Flavia
    Correia, Alexandra
    Figueiredo, Patricia
    Zhang, Hongbo
    Martins, Joao Pedro
    Hirvonen, Jouni T.
    Granja, Pedro
    Sarmento, Bruno
    Santos, Helder A.
    [J]. ADVANCED FUNCTIONAL MATERIALS, 2017, 27 (42)
  • [3] Conjugating Prussian blue nanoparticles onto antigen-specific T cells as a combined nanoimmunotherapy
    Burga, Rachel A.
    Patel, Shabnum
    Bollard, Catherine M.
    Cruz, Conrad Russell Y.
    Fernandes, Rohan
    [J]. NANOMEDICINE, 2016, 11 (14) : 1759 - 1767
  • [4] Photothermal therapy with immune-adjuvant nanoparticles together with checkpoint blockade for effective cancer immunotherapy
    Chen, Qian
    Xu, Ligeng
    Liang, Chao
    Wang, Chao
    Peng, Rui
    Liu, Zhuang
    [J]. NATURE COMMUNICATIONS, 2016, 7
  • [5] Stimuli-responsive nanocomposites for magnetic targeting synergistic multimodal therapy and T1/T2-weighted dual-mode imaging
    Chen, Yinyin
    Deng, Xiaoran
    Li, Chunxia
    He, Fei
    Liu, Bei
    Hou, Zhiyao
    Cheng, Ziyong
    Xing, Bengang
    Lin, Jun
    [J]. NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2017, 13 (03) : 875 - 883
  • [6] Combination of fucoidan-based magnetic nanoparticles and immunomodulators enhances tumour-localized immunotherapy
    Chiang, Chih-Sheng
    Lin, Yu-Jung
    Lee, Rachel
    Lai, Yen-Ho
    Cheng, Hung-Wei
    Hsieh, Chia-Hung
    Shyu, Woei-Cherng
    Chen, San-Yuan
    [J]. NATURE NANOTECHNOLOGY, 2018, 13 (08) : 746 - +
  • [7] PPAR-Induced Fatty Acid Oxidation in T Cells Increases the Number of Tumor-Reactive CD8+ T Cells and Facilitates Anti-PD-1 Therapy
    Chowdhury, Partha S.
    Chamoto, Kenji
    Kumar, Alok
    Honjo, Tasuku
    [J]. CANCER IMMUNOLOGY RESEARCH, 2018, 6 (11) : 1375 - 1387
  • [8] MRI of Tumor-Associated Macrophages with Clinically Applicable Iron Oxide Nanoparticles
    Daldrup-Link, Heike E.
    Golovko, Daniel
    Ruffell, Brian
    DeNardo, David G.
    Castaneda, Rosalinda
    Ansari, Celina
    Rao, Jianghong
    Tikhomirov, Grigory A.
    Wendland, Michael F.
    Corot, Claire
    Coussens, Lisa M.
    [J]. CLINICAL CANCER RESEARCH, 2011, 17 (17) : 5695 - 5704
  • [9] MnFe2O4-decorated large-pore mesoporous silica-coated upconversion nanoparticles for near-infrared light-induced and O2 self-sufficient photodynamic therapy
    Ding, Binbin
    Shao, Shuai
    Xiao, Haihua
    Sun, Chunqiang
    Cai, Xuechao
    Jiang, Fan
    Zhao, Xueyan
    Ma, Ping'an
    Lin, Jun
    [J]. NANOSCALE, 2019, 11 (31) : 14654 - 14667
  • [10] Glioma Morphology and Tumor-Induced Vascular Alterations Revealed in Seven Rodent Glioma Models by In Vivo Magnetic Resonance Imaging and Angiography
    Doblas, Sabrina
    He, Ting
    Saunders, Debbie
    Pearson, Jamie
    Hoyle, Jessica
    Smith, Nataliya
    Lerner, Megan
    Towner, Rheal A.
    [J]. JOURNAL OF MAGNETIC RESONANCE IMAGING, 2010, 32 (02) : 267 - 275