利用PA1094T联合抗cd47抗体的NIR-II光声成像引导化学光热疗法:激活热凋亡治疗原位胶质母细胞瘤。

IF 11 2区 医学 Q1 ENGINEERING, BIOMEDICAL Advanced Healthcare Materials Pub Date : 2024-11-30 DOI:10.1002/adhm.202403108
Shiying Li, Fanchu Zeng, Qi Zhou, Lanqing Li, Hsuan Lo, Jiali Chen, Zhijin Fan, Guojia Huang, Liming Nie
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引用次数: 0

摘要

单药化疗治疗胶质母细胞瘤(GBM)由于药物递送效率低和肿瘤微环境免疫抑制导致耐药,往往是无效的。激活程序性细胞死亡机制和肿瘤相关巨噬细胞向抗肿瘤m1样表型重极化的策略可以帮助逆转免疫抑制的肿瘤微环境。在这项研究中,提出了一种使用NIR-II (1000-1700 nm)光声成像(PAI)引导的化学光热疗法的新方法。NIR-II成像具有优越的组织穿透性和降低背景噪声,能够精确定位肿瘤。利用聚乳酸-羟基乙酸纳米颗粒负载A1094染料和替莫唑胺(TMZ),偶联抗cd47抗体,开发了一种靶向纳米前药。该系统采用NIR-II光激活的协同化学光热疗法,诱导细胞凋亡、焦亡和t细胞活化。PAI提供了快速、即时的GBM诊断,并强调了PA1094T纳米平台的有效靶向性。在复发性GBM模型中,PA1094T联合抗cd47抗体可显著增强癌细胞吞噬能力,有效重塑免疫抑制微环境,治疗效果优于常规治疗。这些结果表明,这种NIR-II pai引导的药物鸡尾酒疗法是治疗GBM的一种很有前景的策略,可能通过增强靶向和免疫调节来解决耐药问题并提高治疗效果。
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NIR-II Photoacoustic Imaging-Guided Chemo-Photothermal Therapy Using PA1094T Combined with Anti-CD47 Antibody: Activating Pyroptosis against Orthotopic Glioblastoma

Treating glioblastoma (GBM) with single-agent chemotherapy is often ineffective due to inefficient drug delivery and the immunosuppressive tumor microenvironment, which leads to drug resistance. Strategies that activate programmed cell death mechanisms and repolarized tumor-associated macrophages toward an antitumoral M1-like phenotype can help reverse the immunosuppressive tumor microenvironment. In this study, a novel approach using NIR-II (1000–1700 nm) photoacoustic imaging (PAI)-guided chemo-photothermal therapy is presented. NIR-II imaging, with its superior tissue penetration and reduced background noise, enables precise tumor targeting. A targeted nano prodrug is developed using poly (lactic-co-glycolic acid) nanoparticles loaded with A1094 dye and temozolomide (TMZ), coupled with an anti-CD47 antibody. This system employs synergistic chemo-photothermal therapy activated by NIR-II light, inducing apoptosis, pyroptosis, and T-cell activation. PAI provides rapid, point-of-care GBM diagnosis, and highlighted the effective targeting of the PA1094T nanoplatform. In a recurrent GBM model, the combination of PA1094T and anti-CD47 antibody significantly enhances cancer cell phagocytosis and effectively remodels the immunosuppressive microenvironment, resulting in better therapeutic outcomes compared to conventional therapies. These results indicate that this NIR-II PAI-guided drug cocktail therapy is a promising strategy for treating GBM, potentially addressing drug resistance and improving treatment efficacy through enhanced targeting and immunomodulation.

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来源期刊
Advanced Healthcare Materials
Advanced Healthcare Materials 工程技术-生物材料
CiteScore
14.40
自引率
3.00%
发文量
600
审稿时长
1.8 months
期刊介绍: Advanced Healthcare Materials, a distinguished member of the esteemed Advanced portfolio, has been dedicated to disseminating cutting-edge research on materials, devices, and technologies for enhancing human well-being for over ten years. As a comprehensive journal, it encompasses a wide range of disciplines such as biomaterials, biointerfaces, nanomedicine and nanotechnology, tissue engineering, and regenerative medicine.
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