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用于肿瘤协同免疫治疗、光疗和化疗的功能性二维铁基纳米片。

Functional 2D Iron-Based Nanosheets for Synergistic Immunotherapy, Phototherapy, and Chemotherapy of Tumor.

机构信息

Laboratory of Chemical Biology, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin, 130022, P. R. China.

School of Applied Chemistry and Engineering, University of Science and Technology of China, Hefei, Anhui, 230026, P. R. China.

出版信息

Adv Healthc Mater. 2022 Oct;11(19):e2200776. doi: 10.1002/adhm.202200776. Epub 2022 Aug 12.

Abstract

Immunotherapy efficacy has been limited by tumor-associated macrophages (TAMs), which are the most abundant immune regulatory cells infiltrating around tumor tissues. The repolarization of pro-tumor M2 TAMs to anti-tumor M1 TAMs is a very promising immunotherapeutic strategy for cancer therapy. In this manuscript, multifunctional 2D iron-based nanosheets (FeNSs) are synthesized via a simple hydrothermal method for the first time, which not only possess photothermal and photodynamic properties, but also can repolarize TAMs from M2 to M1. After modifying with polyethylene glycol and loading with bioreductive prodrug banoxantrone (AQ4N), abbreviated as FeNSs, it can effectively repolarize TAMs from M2 to M1 and deliver AQ4N to tumor microenvironment (TME). Moreover, the repolarized M1 TAMs overexpress inducible nitric oxide synthase, which can convert nontoxic AQ4N to cytotoxic AQ4 under hypoxic TME, enabling immunomodulation-activated chemotherapy. A series of in vitro and in vivo results corroborate that FeNSs effectively exert photothermal and photodynamic effects and repolarize M2 TAMs to M1 TAMs, releasing inflammatory factors and activating the chemotherapeutic effect, thereby realizing synergistic tumor therapy.

摘要

免疫疗法的疗效受到肿瘤相关巨噬细胞(TAMs)的限制,TAMs 是浸润在肿瘤组织周围最丰富的免疫调节细胞。将促肿瘤 M2 TAMs 重极化为抗肿瘤 M1 TAMs 是癌症治疗非常有前途的免疫治疗策略。在本手稿中,首次通过简单的水热法合成了多功能二维铁基纳米片(FeNSs),其不仅具有光热和光动力特性,而且还可以将 TAMs 从 M2 重极化到 M1。用聚乙二醇修饰并装载生物还原前药氨甲喋呤(AQ4N)后,缩写为 FeNSs,可有效将 TAMs 从 M2 重极化到 M1,并将 AQ4N 递送至肿瘤微环境(TME)。此外,重极化的 M1 TAMs 过表达诱导型一氧化氮合酶,可在缺氧 TME 下将无毒的 AQ4N 转化为细胞毒性 AQ4,从而实现免疫调节激活化疗。一系列体外和体内结果证实,FeNSs 可有效发挥光热和光动力作用,并将 M2 TAMs 重极化到 M1 TAMs,释放炎症因子并激活化疗效果,从而实现协同肿瘤治疗。

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