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Theranostics ; 13(12): 4121-4137, 2023.
Article in English | MEDLINE | ID: mdl-37554266

ABSTRACT

Background: Due to the immunosuppressive tumor microenvironment (TME), radiation therapy (RT)-mediated immune response is far from satisfactory. How to improve the efficacy of immunogenic RT by priming strong immunogenic cell death (ICD) is an interesting and urgent challenge. Methods: A polyacrylic acid-coated core-shell UiO@Mn3O4 (denoted as UMP) nanocomposite is constructed for immunogenic RT via multiple strategies. Results: Reshaping the TME via Mn3O4-mediated integration of O2 production, GSH depletion, ROS generation and cell cycle arrest, accompanied by Hf-based UiO-mediated radiation absorption, eventually amplifies UMP-mediated RT to induce intense ICD. With the potent ICD induction and reprogrammed tumor-associated macrophages, this synergetic strategy can promote dendritic cells maturation and CD8+ T cells infiltration, and potentiate anti-tumor immunity against primary, distant, and metastatic tumors. Conclusion: This work is expected to shed light on the immunosuppressive TME-reshaping via multiple strategies to reinforce the immunogenic RT outcome and facilitate the development of effective cancer nanomedicine.


Subject(s)
Cell Death , Nanomedicine , Nanostructures , Neoplasms , Animals , Humans , Mice , CD8-Positive T-Lymphocytes/immunology , Cell Cycle Checkpoints , Cell Death/immunology , Cell Death/radiation effects , Cell Line, Tumor , Dendritic Cells/immunology , Glutathione/metabolism , Mice, Inbred BALB C , Nanomedicine/methods , Nanostructures/chemistry , Nanostructures/therapeutic use , Neoplasm Metastasis/immunology , Neoplasms/immunology , Neoplasms/pathology , Neoplasms/radiotherapy , Oxygen/metabolism , Reactive Oxygen Species/metabolism , Tumor Microenvironment , Tumor-Associated Macrophages/immunology , Xenograft Model Antitumor Assays
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