Beijing Key Laboratory of Molecular Pharmaceutics and New Drug Delivery System, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, PR China.
Beijing Key Laboratory of Molecular Pharmaceutics and New Drug Delivery System, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, PR China.
Biomaterials. 2021 Feb;269:120648. doi: 10.1016/j.biomaterials.2020.120648. Epub 2021 Jan 4.
Phototherapy and immunogenic cell death (ICD) are powerful strategies to fight cancer. However, their therapeutic outcomes are diminished by immunosuppressive and hypoxia microenvironment. Herein, a photo-based, immunomodulating and hypoxia-alleviated nanosystem, PDA-ICG@CAT-DTA-1, is proposed to achieve the synergism between phototherapy and immunotherapy. Catalase (CAT) and anti-GITR antibody (DTA-1) are loaded to photothermal agent and photosensitizer composed PDA-ICG nanoparticles. The PDA-ICG@CAT-DTA-1 exhibits intrinsic local hyperthermia and enhanced ROS generation in tumor, and abrogates tumor immune suppression. It results in reduction of intratumoral FOXP3 regulatory T cells (4.3-fold) and increase of CD4 effector T cells (1.5-fold) compare with the control, and promotes damage associated molecular patterns generation to reinvigorate ICD effect. The potent antitumor of PDA-ICG@CAT-DTA-1 is proved in 4T1 bilateral tumor-bearing mice, with inhibition ratio of 95.1% for primary cancers and 68.7% for abscopal cancers. Our findings highlight great promise of the constructed versatility nanosystem to fix bottlenecks for cancer therapy.
光疗和免疫原性细胞死亡(ICD)是对抗癌症的强大策略。然而,它们的治疗效果受到免疫抑制和缺氧微环境的影响。本文提出了一种基于光的、免疫调节和缓解缺氧的纳米系统 PDA-ICG@CAT-DTA-1,以实现光疗和免疫疗法的协同作用。将过氧化氢酶(CAT)和抗 GITR 抗体(DTA-1)负载到由光热剂和光敏剂组成的 PDA-ICG 纳米颗粒中。PDA-ICG@CAT-DTA-1 在肿瘤中表现出固有局部热疗和增强的 ROS 生成,并消除肿瘤免疫抑制。与对照组相比,它导致肿瘤内 FOXP3 调节性 T 细胞减少 4.3 倍,CD4 效应性 T 细胞增加 1.5 倍,并促进损伤相关分子模式的产生,以重新激活 ICD 效应。PDA-ICG@CAT-DTA-1 在 4T1 双侧荷瘤小鼠中的抗肿瘤作用得到了证明,对原发性肿瘤的抑制率为 95.1%,对远处肿瘤的抑制率为 68.7%。我们的研究结果突出了构建多功能纳米系统克服癌症治疗瓶颈的巨大潜力。