Nanoscale coordination polymers induce immunogenic cell death by amplifying radiation therapy mediated oxidative stress

被引:213
作者
Huang, Zhusheng [1 ,2 ,3 ]
Wang, Yuxiang [1 ,2 ,3 ]
Yao, Dan [1 ,2 ,3 ]
Wu, Jinhui [1 ,2 ,3 ,4 ]
Hu, Yiqiao [1 ,2 ,3 ,4 ]
Yuan, Ahu [1 ,2 ,3 ,4 ]
机构
[1] Nanjing Univ, State Key Lab Pharmaceut Biotechnol, Sch Life Sci, Nanjing 210093, Peoples R China
[2] Nanjing Univ, Med Sch, Nanjing 210093, Peoples R China
[3] Nanjing Univ, Jiangsu Key Lab Nano Technol, Nanjing 210093, Peoples R China
[4] Nanjing Univ, Inst Drug R&D, Med Sch, Nanjing 210093, Peoples R China
关键词
TUMOR MICROENVIRONMENT; PEROXIDASE-ACTIVITY; CANCER-TREATMENT; PD-1; BLOCKADE; T-CELLS; RADIOTHERAPY; NANOPARTICLES; FUTURE; IMMUNOSURVEILLANCE; MECHANISMS;
D O I
10.1038/s41467-020-20243-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Radiation therapy can potentially induce immunogenic cell death, thereby priming anti-tumor adaptive immune responses. However, radiation-induced systemic immune responses are very rare and insufficient to meet clinical needs. Here, we demonstrate a synergetic strategy for boosting radiation-induced immunogenic cell death by constructing gadolinium-hemin based nanoscale coordination polymers to simultaneously perform X-ray deposition and glutathione depletion. Subsequently, immunogenic cell death is induced by sensitized radiation to potentiate checkpoint blockade immunotherapies against primary and metastatic tumors. In conclusion, nanoscale coordination polymers-sensitized radiation therapy exhibits biocompatibility and therapeutic efficacy in preclinical cancer models, and has the potential for further application in cancer radio-immunotherapy. Radiotherapy has the potential to induce immunogenic cell death (ICD), however radiation-induced immune responses are often limited. Here the authors design gadolinium-based nanoscale coordination polymers to amplify radiation-mediated oxidative stress, promoting ICD and anti-tumor immune responses.
引用
收藏
页数:18
相关论文
共 65 条
  • [1] Systematic review of case reports on the abscopal effect
    Abuodeh, Yazan
    Venkat, Puja
    Kim, Sungjune
    [J]. CURRENT PROBLEMS IN CANCER, 2016, 40 (01) : 25 - 37
  • [2] BANSAL A, 2018, CHEM REV, V217, P2291, DOI DOI 10.1083/JCB.201804161
  • [3] The tumour microenvironment after radiotherapy: mechanisms of resistance and recurrence
    Barker, Holly E.
    Paget, James T. E.
    Khan, Aadil A.
    Harrington, Kevin J.
    [J]. NATURE REVIEWS CANCER, 2015, 15 (07) : 409 - 425
  • [4] Normal tissue reactions to radiotherapy: towards tailoring treatment dose by genotype
    Barnett, Gillian C.
    West, Catherine M. L.
    Dunning, Alison M.
    Elliott, Rebecca M.
    Coles, Charlotte E.
    Pharoah, Paul D. P.
    Burnet, Neil G.
    [J]. NATURE REVIEWS CANCER, 2009, 9 (02) : 134 - 142
  • [5] Behrend L, 2003, BIOCHEM SOC T, V31, P1441
  • [6] Bernhard EJ, 2000, CANCER RES, V60, P86
  • [7] CD4+ T cell help in cancer immunology and immunotherapy
    Borst, Jannie
    Ahrends, Tomasz
    Babala, Nikolina
    Melief, Cornelis J. M.
    Kastenmueller, Wolfgang
    [J]. NATURE REVIEWS IMMUNOLOGY, 2018, 18 (10) : 635 - 647
  • [8] Oncology Meets Immunology: The Cancer-Immunity Cycle
    Chen, Daniel S.
    Mellman, Ira
    [J]. IMMUNITY, 2013, 39 (01) : 1 - 10
  • [9] Curiel T.J., 2007, Tregs and rethinking cancer immunotherapy Find the latest version: Review series personal perspective Tregs and rethinking cancer immunotherapy, V117, P1167, DOI DOI 10.1172/JCI31202
  • [10] The role of radiotherapy in cancer treatment - Estimating optimal utilization from a review of evidence-based clinical guidelines
    Delaney, G
    Jacob, S
    Featherstone, C
    Barton, M
    [J]. CANCER, 2005, 104 (06) : 1129 - 1137