Nano‐Engineered Magnesium Implants for Magnetothermal Enhanced Pyroptosis to Boost Immunotherapy

Author:

Han Xiao12,Sun Shumin3,Yang Nailin34,Han Zhihui3,Pei Zifan3,Yu Qiao3,Nie Jihu3,Wang Li3,Liu Anhong12,Meng Xiangxue12,Wang Zhanhui125,Cheng Liang34ORCID

Affiliation:

1. Luoyang Key Laboratory of Basic and Clinical Application Research of Biomaterials Luoyang Central Hospital affiliated to Zhengzhou University Luoyang 471000 China

2. Henan Provincial Health Commission Key Laboratory of Tumor Nanotechnology Luoyang Central Hospital affiliated to Zhengzhou University Luoyang 471000 China

3. Institute of Functional Nano & Soft Materials (FUNSOM) Jiangsu Key Laboratory for Carbon‐Based Functional Materials and Devices Soochow University Suzhou 215123 China

4. Macao Institute of Materials Science and Engineering Macau University of Science and Technology Taipa Macau SAR 999078 China

5. Henan International Joint Laboratory of Tumor Cell Immunity and Regenerative Medicine Luoyang Central Hospital affiliated to Zhengzhou University Luoyang 471000 China

Abstract

Abstract Hepatocellular carcinoma (HCC) is one of the leading contributors to cancer‐related death because the immunosuppressive tumor microenvironment (TME) limits its therapeutic efficacy. Gasdermin (GSDM)‐mediated pyroptosis is a new programmed cell death that can boost antitumor immune responses. However, inducing efficient pyroptosis to reverse the immunosuppressive TME is challenging. Herein, layered double hydroxide‐coated magnesium (Zn‐LDH@Mg) implants are designed and constructed as alternating magnetic field (AMF)‐activated pyroptosis inducers to induce highly effective pyroptosis in cancer cells. The powerful eddy‐thermal effects of Zn‐LDH@Mg implants markedly amplify pyroptosis in malignant cells through the Caspase‐1/GSDMD‐dependent canonical pathway. Moreover, Mg2+ and pyroptosis synergistically activate T cells (especially CD8+ T cells) and enhance the infiltration of immune‐supportive cells. This innovative strategy not only significantly suppresses the proliferation of the primary tumor but also stimulates the immune response to further enhance the efficacy of immune checkpoint inhibitors and impede the progression of distant tumors. This work not only emphasizes the importance of surface engineering strategies for the preparation of novel pyroptosis inducers but also highlights the effectiveness of the strategy in reversing the immunosuppressive TME to enhance immunotherapy, providing a new approach for the rational design of bioactive materials to increase the efficacy of immunotherapy.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Higher Education Discipline Innovation Project

Publisher

Wiley

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