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Catalytical nano-immunocomplexes for remote-controlled sono-metabolic checkpoint trimodal cancer therapy

Author

Listed:
  • Chi Zhang

    (Nanyang Technological University)

  • Jingsheng Huang

    (Nanyang Technological University)

  • Ziling Zeng

    (Nanyang Technological University)

  • Shasha He

    (Nanyang Technological University)

  • Penghui Cheng

    (Nanyang Technological University)

  • Jingchao Li

    (Nanyang Technological University)

  • Kanyi Pu

    (Nanyang Technological University
    Nanyang Technological University
    Nanyang Technological University)

Abstract

Checkpoint immunotherapies have been combined with other therapeutic modalities to increase patient response rate and improve therapeutic outcome, which however exacerbates immune-related adverse events and requires to be carefully implemented in a narrowed therapeutic window. Strategies for precisely controlled combinational cancer immunotherapy can tackle this issue but remain lacking. We herein report a catalytical nano-immunocomplex for precise and persistent sono-metabolic checkpoint trimodal cancer therapy, whose full activities are only triggered by sono-irradiation in tumor microenvironment (TME). This nano-immunocomplex comprises three FDA-approved components, wherein checkpoint blockade inhibitor (anti-programmed death-ligand 1 antibody), immunometabolic reprogramming enzyme (adenosine deaminase, ADA), and sonosensitizer (hematoporphyrin) are covalently immobilized into one entity via acid-cleavable and singlet oxygen-activatable linkers. Thus, the activities of the nano-immunocomplex are initially silenced, and only under sono-irradiation in the acidic TME, the sonodynamic, checkpoint blockade, and immunometabolic reprogramming activities are remotely awakened. Due to the enzymatic conversion of adenosine to inosine by ADA, the nano-immunocomplex can reduce levels of intratumoral adenosine and inhibit A2A/A2B adenosine receptors-adenosinergic signaling, leading to efficient activation of immune effector cells and inhibition of immune suppressor cells in vivo. Thus, this study presents a generic and translatable nanoplatform towards precision combinational cancer immunotherapy.

Suggested Citation

  • Chi Zhang & Jingsheng Huang & Ziling Zeng & Shasha He & Penghui Cheng & Jingchao Li & Kanyi Pu, 2022. "Catalytical nano-immunocomplexes for remote-controlled sono-metabolic checkpoint trimodal cancer therapy," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-31044-6
    DOI: 10.1038/s41467-022-31044-6
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    1. Akio Ohta & Michail Sitkovsky, 2001. "Role of G-protein-coupled adenosine receptors in downregulation of inflammation and protection from tissue damage," Nature, Nature, vol. 414(6866), pages 916-920, December.
    2. Chi Zhang & Ziling Zeng & Dong Cui & Shasha He & Yuyan Jiang & Jingchao Li & Jiaguo Huang & Kanyi Pu, 2021. "Semiconducting polymer nano-PROTACs for activatable photo-immunometabolic cancer therapy," Nature Communications, Nature, vol. 12(1), pages 1-12, December.
    3. Yuyan Jiang & Jiaguo Huang & Cheng Xu & Kanyi Pu, 2021. "Activatable polymer nanoagonist for second near-infrared photothermal immunotherapy of cancer," Nature Communications, Nature, vol. 12(1), pages 1-14, December.
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    1. Dongdong Wang & Jiawei Liu & Changlai Wang & Weiyun Zhang & Guangbao Yang & Yun Chen & Xiaodong Zhang & Yinglong Wu & Long Gu & Hongzhong Chen & Wei Yuan & Xiaokai Chen & Guofeng Liu & Bin Gao & Qianw, 2023. "Microbial synthesis of Prussian blue for potentiating checkpoint blockade immunotherapy," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
    2. Yongjiang Li & Wei Chen & Yong Kang & Xueyan Zhen & Zhuoming Zhou & Chuang Liu & Shuying Chen & Xiangang Huang & Hai-Jun Liu & Seyoung Koo & Na Kong & Xiaoyuan Ji & Tian Xie & Wei Tao, 2023. "Nanosensitizer-mediated augmentation of sonodynamic therapy efficacy and antitumor immunity," Nature Communications, Nature, vol. 14(1), pages 1-17, December.

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