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Combination of NIR therapy and regulatory T cell modulation using layer-by-layer hybrid nanoparticles for effective cancer photoimmunotherapy

机译:NIR治疗和调节性T细胞调节的组合,使用逐层混合纳米颗粒进行有效的癌症光免疫治疗

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The efficacy of combined near-infrared (NIR) and immune therapies for inhibiting tumor growth and recurrence has gained increasing research attention. Regulatory T cells in the tumor microenvironment constitute a major obstacle in achieving robust CD8+ T cell antitumor immunotherapy. In the present study, we designed a photoimmunotherapy-based strategy involving a combination of photothermal and photodynamic therapies, followed by Treg cell suppression, for eliciting an immune response with IR-780- and imatinib-loaded layer-by-layer hybrid nanoparticles. Methods: The layer-by-layer hybrid nanoparticles were prepared through electrostatic interactions. Their photothermal effect, photodynamic effect as well as their effect on inhibiting Treg cells' suppressive function were investigated in vitro and in vivo . Their antitumor effect was evaluated using B16/BL6 and MC-38 tumor-bearing mice. Results: The layer-by-layer hybrid nanoparticles, which were pH-sensitive, enabled the release of IR-780 dye for NIR-induced photothermal and photodynamic effects, and the release of imatinib-loaded glucocorticoid-induced TNF receptor family-related protein/poly(lactic-co-glycolic acid) (GITR-PLGA) nanoparticles to initiate antitumor immunotherapy. The photothermal and photodynamic effects caused by IR-780 under NIR exposure resulted in direct tumor apoptosisecrosis and the production of tumor-associated antigen, promoted dendritic cell maturation, and enhanced the presentation of tumor-associated antigen to T cells, while the imatinib-loaded GITR-PLGA cores reduced the suppressive function of Treg cells, and consequently activated effective CD8+ T cells towards tumors. Conclusion: With the significant photothermal, photodynamic and immunotherapies, the system successfully eradicated tumor growth, diminished tumor recurrence, and improved survival in vivo . The proposed nanoparticles provide a novel and versatile approach to boost antitumor photoimmunotherapy.
机译:近红外(NIR)和免疫疗法联合用于抑制肿瘤生长和复发的功效已引起越来越多的研究关注。肿瘤微环境中的调节性T细胞构成了实现可靠的CD8 + T细胞抗肿瘤免疫疗法的主要障碍。在本研究中,我们设计了一种基于光免疫疗法的策略,包括将光热疗法与光动力疗法相结合,然后抑制Treg细胞,以引发与IR-780和伊马替尼负载的逐层混合纳米颗粒的免疫反应。方法:通过静电相互作用制备层状杂化纳米粒子。在体外和体内研究了它们的光热作用,光动力作用以及它们抑制Treg细胞抑制功能的作用。使用B16 / BL6和MC-38荷瘤小鼠评估了它们的抗肿瘤作用。结果:对pH敏感的逐层杂化纳米颗粒能够释放IR-780染料以产生NIR诱导的光热和光动力效应,并释放载有伊马替尼的糖皮质激素诱导的TNF受体家族相关蛋白/聚(乳酸-乙醇酸共聚物)(GITR-PLGA)纳米颗粒可启动抗肿瘤免疫治疗。在近红外照射下,IR-780引起的光热和光动力效应导致肿瘤直接凋亡/坏死和肿瘤相关抗原的产生,促进树突状细胞成熟,并增强肿瘤相关抗原向T细胞的呈递,而伊马替尼载有GITR-PLGA的核降低了Treg细胞的抑制功能,因此激活了有效的CD8 + T细胞对肿瘤。结论:通过重要的光热,光动力和免疫疗法,该系统成功消除了肿瘤的生长,减少了肿瘤的复发,并提高了体内存活率。提出的纳米粒子提供了一种新颖且通用的方法来增强抗肿瘤光免疫疗法。

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