Magnetic Drug Delivery System Capable of Remodeling the Tumor Immune Microenvironment for Photothermal Immunotherapy/Chemotherapy

Innovative therapeutic strategies are urgently needed to address the challenges posed by the limited efficacy of monotherapies and the ineffective immune response of "cold" tumors. To address this, a multifunctional magnetic drug delivery system (MDDS) is designed utilizing polydopamine-coated Fe<sub>3</sub>O<sub>4</sub> magnetic nanoparticles. This system is capable of loading the chemotherapeutic drug doxorubicin (DOX) and the OTU deubiquitinating enzyme 2 inhibitor LN5P45 through a sophisticated design. The MDDS not only enables targeted drug delivery using magnetic forces but also promotes tumor destruction and enhances the immunogenic cell death effect by leveraging photothermal properties when exposed to laser irradiation. Furthermore, it triggers a robust anti-tumor immune response by disrupting the endoplasmic reticulum protein degradation pathway, which specifically reduces programmed death-ligand 1 expression on the surfaces of tumor cells in combination with LN5P45. Experimental results demonstrated that this MDDS-mediated photothermal immunotherapy/chemotherapy can simultaneously activate both innate and adaptive immunity, enhance the infiltration of cytotoxic T-lymphocytes in both primary and distal tumors, and remodel the tumor immune microenvironment. This study presents a multifunctional MDDS that offers a novel approach to optimizing tumor immunotherapy and showcases significant potential for clinical application.

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Publication Details

Journal
Advanced Healthcare Materials
Published
2025-06-16
DOI
https://doi.org/10.1002/adhm.202501088
Citations
3
Primary Topic
Nanoplatforms for cancer theranostics
Type
article
Field-Weighted Citation Impact
2.02

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article

Magnetic Drug Delivery System Capable of Remodeling the Tumor Immune Microenvironment for Photothermal Immunotherapy/Chemotherapy

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3 citations
Advanced Healthcare Materials
Nanoplatforms for cancer theranostics
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article

Magnetic Drug Delivery System Capable of Remodeling the Tumor Immune Microenvironment for Photothermal Immunotherapy/Chemotherapy

Shikang Liu, Qiaoli Feng, Jiarong Liang, Zhiyi Wang, Lujia Chen, Meng‐Die Duan
article en
3 citations

Abstract

Innovative therapeutic strategies are urgently needed to address the challenges posed by the limited efficacy of monotherapies and the ineffective immune response of "cold" tumors. To address this, a multifunctional magnetic drug delivery system (MDDS) is designed utilizing polydopamine-coated Fe<sub>3</sub>O<sub>4</sub> magnetic nanoparticles. This system is capable of loading the chemotherapeutic drug doxorubicin (DOX) and the OTU deubiquitinating enzyme 2 inhibitor LN5P45 through a sophisticated design. The MDDS not only enables targeted drug delivery using magnetic forces but also promotes tumor destruction and enhances the immunogenic cell death effect by leveraging photothermal properties when exposed to laser irradiation. Furthermore, it triggers a robust anti-tumor immune response by disrupting the endoplasmic reticulum protein degradation pathway, which specifically reduces programmed death-ligand 1 expression on the surfaces of tumor cells in combination with LN5P45. Experimental results demonstrated that this MDDS-mediated photothermal immunotherapy/chemotherapy can simultaneously activate both innate and adaptive immunity, enhance the infiltration of cytotoxic T-lymphocytes in both primary and distal tumors, and remodel the tumor immune microenvironment. This study presents a multifunctional MDDS that offers a novel approach to optimizing tumor immunotherapy and showcases significant potential for clinical application.

Advanced Healthcare MaterialsVol. 14(22)
Sun Yat-sen University (CN), Nanfang Hospital (CN), Southern Medical University (CN), South China University of Technology (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Good health and well-being
Openalex Percentile: Top 14%
Nanoplatforms for cancer theranostics
2.02
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