CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Engineered macrophage-derived cellular vesicles for NIR-II fluorescence imaging-guided precise cancer photo-immunotherapy.
Engineered macrophage-derived cellular vesicles for NIR-II fluorescence imaging-guided precise cancer photo-immunotherapy.
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癌症免疫治疗已取得显著进展,但患者间差异、治疗反应有限和严重副作用等挑战依然存在。尽管纳米免疫治疗已成为一种有前景的方法,但构建精准高效纳米系统仍是艰巨挑战。
在此,我们利用巨噬细胞来源的细胞囊泡(MCVs)开发了一种多功能纳米平台,用于NIR-II成像引导的精准癌症光免疫治疗。MCVs表现出优异的肿瘤靶向和TAMs再教育效果,既可作为递送载体又可作为治疗剂。通过酰胺键,将吲哚菁绿(ICG)偶联到MCVs表面,实现了对MCVs体内分布的追踪。
值得注意的是,ICG表现出作为NIR-II荧光剂的双重功能,并具有光动力和光热效应,能够将光能转化为化学能或热能以消除肿瘤细胞。这种精准光疗触发了肿瘤的免疫原性细胞死亡(ICD),从而激活抗肿瘤免疫反应。
此外,负载R848(一种toll样受体激动剂)的MCVs增强了ICD诱导的抗肿瘤免疫。动物实验证实,MCVs介导的光免疫治疗促进了T细胞浸润,抑制了肿瘤生长,并提高了生存率。
总之,我们开发了一种有前景的精准免疫治疗策略,能够增强免疫反应,同时减轻脱靶效应。这些发现为临床转化提供了令人鼓舞的前景。
Significant progress has been made in cancer immunotherapy; however, challenges such as interpatient variability, limited treatment response, and severe side effects persist. Although nanoimmunotherapy has emerged as a promising approach, the construction of precise and efficient nanosystems remain formidable challenges.
Herein, a multifunctional nanoplatform was developed using macrophage-derived cellular vesicles (MCVs) for NIR-II imaging-guided precise cancer photo-immunotherapy. MCVs exhibited excellent tumor targeting and TAMs re-education effects, serving as both delivery carriers and therapeutic agents. Through amide bond, indocyanine green (ICG) was conjugated to the surface of MCVs, enabling in vivo tracking of MCVs distribution.
Notably, ICG exhibited dual functionality as a NIR-II fluorescent agent and possessed photodynamic and photothermal effects, enabling the conversion of light energy into chemical or heat energy to eliminate tumor cells. This precision phototherapy triggered immunogenic cell death (ICD) of tumor, thereby activating the anti-tumor immune response.
Additionally, MCVs loaded with R848, a toll-like receptor agonist, augmented the ICD-induced anti-tumor immunity. Animal experiments confirmed that MCVs-mediated photoimmunotherapy promoted T cell infiltration, inhibited tumor growth, and improved survival rates.
In conclusion, we have developed a promising precision immunotherapy strategy capable of enhancing the immune response while mitigating off-target effects.
These findings offer encouraging prospects for clinical translation.
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