工程纳米微热亡发生器:磁-金属-免疫治疗策略,以加强经动脉栓塞。

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Di Wang, Linzhu Zhang, Jihu Nie, Nailin Yang, Shumin Sun, Chunjie Wang, Zifan Pei, Fei Gong, Xingwei Sun, Yong Jin, Liang Cheng
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引用次数: 0

摘要

气凝胶介导的焦亡是一种很有前途的免疫治疗策略,但需要精确的肿瘤特异性激活。磁热疗法(MHT)在肝细胞癌(HCC)中具有诱导凋亡的潜力,但其疗效受到加热效率不佳和肿瘤耐药性的限制。在此,我们开发了一种创新的磁金属免疫治疗平台,通过工程纳米微热亡发生器,从而增强经动脉栓塞(TAE)。通过组成和结构优化,获得了具有增强磁热性能的Zn-Fe3O4@Co-Fe3O4核壳纳米立方(ZnCo-Fe3O4 CSNCs),其饱和磁化强度(Ms)和矫顽力(Hc)均有显著提高。这些纳米立方体通过微流控技术进一步组装成可调节大小的磁性微球(MSs),整合了TAE和MHT的治疗功能。在交变磁场(AMF)下,ZnCo-Fe3O4 MSs表现出温度依赖性的离子释放和局部热疗,同时通过代谢干扰抑制热休克蛋白(HSP)的上调。这种精心安排的治疗级联有效地触发了癌细胞的焦亡,随后激活了免疫反应,从而提高了磁金属免疫治疗的疗效。该平台与免疫检查点阻断(immune checkpoint blockade, ICB)疗法的战略结合,引发了全面的全身免疫激活,显著提高了治疗效果,抑制了原发肿瘤和远处肿瘤的进展。值得注意的是,ZnCo-Fe3O4 MSs表现出特殊的调节免疫抑制肿瘤生态位的能力,同时通过其独特的栓塞-免疫调节功能显著提高TAE的性能。总之,本研究强调了探索热分解介导的磁金属免疫疗法用于有效癌症治疗的新途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Engineered Nano-Micro Pyroptosis Generators: A Magnetic-Metallo-Immunotherapeutic Strategy to Reinforce Transarterial Embolization.

Gasdermin-mediated pyroptosis represents a promising immunotherapeutic strategy, yet requires precise tumor-specific activation. Magnetic hyperthermia therapy (MHT) has the potential to induce pyroptosis in hepatocellular carcinoma (HCC), while its efficacy is limited by suboptimal heating efficiency and tumor resistance. Herein, we developed an innovative magnetic-metallo-immunotherapeutic platform by engineering nanomicro pyroptosis generators, thereby enhancing transarterial embolization (TAE). Through compositional and structural optimization, Zn-Fe3O4@Co-Fe3O4 core-shell nanocubes (ZnCo-Fe3O4 CSNCs) with enhanced magnetothermal properties were obtained, which exhibited significantly improved saturation magnetization (Ms) and coercivity (Hc). These nanocubes were further assembled via microfluidic technology into magnetic microspheres (MSs) with tunable sizes, integrating the therapeutic functions of TAE and MHT. Under an alternating magnetic field (AMF), the ZnCo-Fe3O4 MSs demonstrated temperature-dependent ion release and localized hyperthermia while simultaneously inhibiting heat shock protein (HSP) upregulation through metabolic interference. This orchestrated therapeutic cascade effectively triggered pyroptosis in cancer cells, subsequently activating the immune response and thereby enhancing the efficacy of magnetic-metallo-immunotherapy. The strategic combination of this platform with immune checkpoint blockade (ICB) therapy provoked comprehensive systemic immune activation, markedly enhancing treatment efficacy and suppressing the progression of both primary tumors and distant tumors. Notably, ZnCo-Fe3O4 MSs demonstrated an exceptional capacity to modulate the immunosuppressive tumor niche while substantially improving TAE performance through their unique embolization-immunomodulation functionality. Overall, this study highlights new avenues for exploring pyroptosis-mediated magnetic-metallo-immunotherapy for effective cancer therapy.

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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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