肿瘤光免疫治疗的内源性纳米平台:缺氧调节和STING通路激活。

Yongqing Yang, Ni Shao, Qiao Luo, Nianlan Cheng, Jifeng Chen, Yanyu Huang, Cuiqing Huang, Jiang Ouyang, Liangping Luo, Zeyu Xiao
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摘要

光免疫疗法(PIT)由于其空间精度和持续的治疗效果,在癌症治疗中具有重要的前景。然而,克服肿瘤微环境(TME)的免疫抑制和缺氧仍然是一个主要挑战。为了解决这个问题,我们开发了一个多功能的PIT纳米平台(BYMnNps)。其组成具有不同的作用:1)胆绿素可诱导轻度光热和光动力治疗,增强纳米平台对肿瘤的渗透,诱导免疫原性细胞死亡;Ii)免疫治疗肽酪serletide诱导肿瘤细胞凋亡,增强肿瘤特异性免疫应答;iii) Mn 2⁺可以催化过氧化氢生成氧气,减少肿瘤缺氧,同时激活cGAS-STING通路,进一步促进癌症免疫治疗。纳米平台显著抑制肿瘤生长,增加肿瘤对α-PD - 1治疗的敏感性。值得注意的是,BYMnNps还具有光声和磁共振成像能力。综上所述,BYMnNps能有效对抗肿瘤免疫抑制,缓解TME缺氧,具有良好的生物相容性和抗肿瘤功效,在多模态成像指导下的精准癌症治疗中具有广阔的潜力。意义声明:光免疫疗法因其空间精度和持续治疗效果而在癌症治疗中具有很大的前景。然而,光疗诱导的肿瘤缺氧导致抵抗,提出了重大挑战。本研究利用内源性光敏剂胆绿素、免疫治疗肽酪氨酸和Mn 2⁺自组装成多功能纳米粒子,旨在同时逆转肿瘤微环境的免疫抑制和缓解缺氧。具有良好的生物安全性和抗肿瘤疗效,可增强肿瘤对α-PD1治疗的敏感性。此外,它还具有光声和磁共振成像能力,显示出在多模态成像指导下精确癌症治疗的广阔潜力。它有可能克服目前光免疫疗法的局限性,为癌症治疗提供新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endogenous nanoplatforms for tumor photoimmunotherapy: Hypoxia modulation and STING pathway activation.

Photoimmunotherapy (PIT) holds significant promise for cancer treatment due to its spatial precision and sustained therapeutic effects. However, overcoming the immunosuppression and hypoxia of the tumor microenvironment (TME) remains a major challenge. To solve this problem, we developed a multifunctional PIT nanoplatform (BYMnNps). Its composition plays different roles: i) Biliverdin can induce mild photothermal and photodynamic therapy, enhance the penetration of nanoplatforms into tumors, and induce immunogenic cell death; ii) the immunotherapy peptide tyroserleutide induces tumor cell apoptosis and enhances tumor-specific immune responses; iii) Mn²⁺ can catalyze the generation of oxygen from hydrogen peroxide, reducing tumor hypoxia, while activating the cGAS-STING pathway, further boosting cancer immunotherapy. The nanoplatforms significantly inhibit tumor growth and increase tumor sensitivity to α-PD 1 therapy. Notably, BYMnNps also exhibit photoacoustic and magnetic resonance imaging capabilities. Overall, BYMnNps effectively counteract tumor immune suppression and alleviates TME hypoxia, demonstrating good biocompatibility and antitumor efficacy, with broad potential for precision cancer treatment guided by multimodal imaging. STATEMENT OF SIGNIFICANCE: Photoimmunotherapy holds great promise for cancer treatment due to its spatial precision and sustained therapeutic effects. However, phototherapy-induced tumor hypoxia leads to resistance, posing a significant challenge. This study utilizes endogenous photosensitizer biliverdin, immunotherapy peptide tyroserleutide, and Mn²⁺ to self-assemble into a multifunctional nanoparticle, aimed at simultaneously reversing the immunosuppression of the tumor microenvironment and alleviating hypoxia. It demonstrates good biosafety and antitumor efficacy, enhancing tumor sensitivity to α-PD1 therapy. Additionally, it exhibits photoacoustic and magnetic resonance imaging capabilities, showing broad potential for precision cancer treatment guided by multimodal imaging. It has the potential to overcome the current limitations of photoimmunotherapy, offering a new avenue for cancer treatment.

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