Ruoping Wang, Junpeng Shi*, Xiaofang Luo, Xia Sun, Yuan-Yuan Zhu, Ping’an Ma, Jun Lin* and Yun Zhang*,
{"title":"磁性持续发光纳米颗粒重新极化肿瘤相关巨噬细胞以增强癌症免疫治疗","authors":"Ruoping Wang, Junpeng Shi*, Xiaofang Luo, Xia Sun, Yuan-Yuan Zhu, Ping’an Ma, Jun Lin* and Yun Zhang*, ","doi":"10.1021/acsmaterialslett.5c0017010.1021/acsmaterialslett.5c00170","DOIUrl":null,"url":null,"abstract":"<p >M2-like tumor-associated macrophages (M2-TAMs) are key factors in creating an immunosuppressive tumor microenvironment (TME). Transforming M2-TAMs to immunostimulatory M1-TAMs is essential to reverse the immunosuppressive state of the TME. Herein, we develop a TAM nanopolarization regulator (mZ@ZFR@CM) by loading persistent luminescence nanoparticles, magnetic nanoparticles ZnFe<sub>2</sub>O<sub>4</sub> and R848 in mesoporous silica while wrapping tumor cell membrane, which efficiently converts M2-TAMs to M1-TAMs. We first discovered that ZnFe<sub>2</sub>O<sub>4</sub> has excellent M2-TAM repolarization capability. Furthermore, high-sensitivity persistent luminescence imaging confirms the efficient accumulation of mZ@ZFR@CM in tumor, significantly improving M2-TAM repolarization efficiency. In vivo assays demonstrate that mZ@ZFR@CM induces efficient repolarization of M2-TAMs and successfully reverses the immunosuppressive TME. Assisted by anti-PD-L1, mZ@ZFR@CM triggers a potent antitumor immune response, significantly inhibits tumor growth, and further initiates a specific antitumor immune memory response, providing protection against tumor recurrence and metastasis. This study demonstrates an efficient nanopolarization regulator of TAMs to reverse the immunosuppressive TME.</p>","PeriodicalId":19,"journal":{"name":"ACS Materials Letters","volume":"7 6","pages":"2094–2104 2094–2104"},"PeriodicalIF":8.7000,"publicationDate":"2025-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Magnetic Persistent Luminescence Nanoparticles Repolarize Tumor-Associated Macrophages for Enhanced Cancer Immunotherapy\",\"authors\":\"Ruoping Wang, Junpeng Shi*, Xiaofang Luo, Xia Sun, Yuan-Yuan Zhu, Ping’an Ma, Jun Lin* and Yun Zhang*, \",\"doi\":\"10.1021/acsmaterialslett.5c0017010.1021/acsmaterialslett.5c00170\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >M2-like tumor-associated macrophages (M2-TAMs) are key factors in creating an immunosuppressive tumor microenvironment (TME). Transforming M2-TAMs to immunostimulatory M1-TAMs is essential to reverse the immunosuppressive state of the TME. Herein, we develop a TAM nanopolarization regulator (mZ@ZFR@CM) by loading persistent luminescence nanoparticles, magnetic nanoparticles ZnFe<sub>2</sub>O<sub>4</sub> and R848 in mesoporous silica while wrapping tumor cell membrane, which efficiently converts M2-TAMs to M1-TAMs. We first discovered that ZnFe<sub>2</sub>O<sub>4</sub> has excellent M2-TAM repolarization capability. Furthermore, high-sensitivity persistent luminescence imaging confirms the efficient accumulation of mZ@ZFR@CM in tumor, significantly improving M2-TAM repolarization efficiency. In vivo assays demonstrate that mZ@ZFR@CM induces efficient repolarization of M2-TAMs and successfully reverses the immunosuppressive TME. Assisted by anti-PD-L1, mZ@ZFR@CM triggers a potent antitumor immune response, significantly inhibits tumor growth, and further initiates a specific antitumor immune memory response, providing protection against tumor recurrence and metastasis. This study demonstrates an efficient nanopolarization regulator of TAMs to reverse the immunosuppressive TME.</p>\",\"PeriodicalId\":19,\"journal\":{\"name\":\"ACS Materials Letters\",\"volume\":\"7 6\",\"pages\":\"2094–2104 2094–2104\"},\"PeriodicalIF\":8.7000,\"publicationDate\":\"2025-05-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Materials Letters\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsmaterialslett.5c00170\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Materials Letters","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsmaterialslett.5c00170","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Magnetic Persistent Luminescence Nanoparticles Repolarize Tumor-Associated Macrophages for Enhanced Cancer Immunotherapy
M2-like tumor-associated macrophages (M2-TAMs) are key factors in creating an immunosuppressive tumor microenvironment (TME). Transforming M2-TAMs to immunostimulatory M1-TAMs is essential to reverse the immunosuppressive state of the TME. Herein, we develop a TAM nanopolarization regulator (mZ@ZFR@CM) by loading persistent luminescence nanoparticles, magnetic nanoparticles ZnFe2O4 and R848 in mesoporous silica while wrapping tumor cell membrane, which efficiently converts M2-TAMs to M1-TAMs. We first discovered that ZnFe2O4 has excellent M2-TAM repolarization capability. Furthermore, high-sensitivity persistent luminescence imaging confirms the efficient accumulation of mZ@ZFR@CM in tumor, significantly improving M2-TAM repolarization efficiency. In vivo assays demonstrate that mZ@ZFR@CM induces efficient repolarization of M2-TAMs and successfully reverses the immunosuppressive TME. Assisted by anti-PD-L1, mZ@ZFR@CM triggers a potent antitumor immune response, significantly inhibits tumor growth, and further initiates a specific antitumor immune memory response, providing protection against tumor recurrence and metastasis. This study demonstrates an efficient nanopolarization regulator of TAMs to reverse the immunosuppressive TME.
期刊介绍:
ACS Materials Letters is a journal that publishes high-quality and urgent papers at the forefront of fundamental and applied research in the field of materials science. It aims to bridge the gap between materials and other disciplines such as chemistry, engineering, and biology. The journal encourages multidisciplinary and innovative research that addresses global challenges. Papers submitted to ACS Materials Letters should clearly demonstrate the need for rapid disclosure of key results. The journal is interested in various areas including the design, synthesis, characterization, and evaluation of emerging materials, understanding the relationships between structure, property, and performance, as well as developing materials for applications in energy, environment, biomedical, electronics, and catalysis. The journal has a 2-year impact factor of 11.4 and is dedicated to publishing transformative materials research with fast processing times. The editors and staff of ACS Materials Letters actively participate in major scientific conferences and engage closely with readers and authors. The journal also maintains an active presence on social media to provide authors with greater visibility.