Institute of Molecular Sciences and Engineering, Institute of Frontier and Interdisciplinary Science, Shandong University, Qingdao, 266237, P. R. China.
State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, 130022, P. R. China.
Adv Sci (Weinh). 2022 Nov;9(31):e2202332. doi: 10.1002/advs.202202332. Epub 2022 Sep 25.
Notwithstanding immune checkpoint blocking (ICB) therapy has made eminent clinical breakthroughs, overcoming immunologically "cold" tumors remains challenging. Here, a cascade potentiated nanomodulator AuPtAg-GOx is engineered for boosting immune responsiveness. Upon 1064 nm laser irradiation, AuPtAg-mediated mild photothermal therapy (PTT) activates cytotoxic T lymphocytes and reverses the immunogenic "cold" tumor microenvironment. Further, to amplify the thermal sensitivity of tumor cells, glucose oxidase (GOx) is introduced to suppress the production of heat shock proteins, thereby promoting mild photothermal therapy. Complementarily, AuPtAg nanozymes with catalase-like activity can ameliorate tumor hypoxia, significantly improving the GOx activity. As a result, the combination of AuPtAg-GOx with self-augmented photothermal ability and PD-L1 antibody can further escalate the antitumor efficacy. The AuPtAg-GOx-based synergistic starvation therapy, mild PTT, and immunotherapy cascade enhancement therapy strategy can be a favorable tool to effectively kill cancer cells.
尽管免疫检查点阻断 (ICB) 疗法取得了显著的临床突破,但克服免疫“冷”肿瘤仍然具有挑战性。在这里,设计了一种级联增强型纳米调节剂 AuPtAg-GOx,用于增强免疫反应性。在 1064nm 激光照射下,AuPtAg 介导的温和光热疗法 (PTT) 激活细胞毒性 T 淋巴细胞并逆转免疫原性“冷”肿瘤微环境。此外,为了放大肿瘤细胞的热敏感性,引入葡萄糖氧化酶 (GOx) 以抑制热休克蛋白的产生,从而促进温和的光热疗法。此外,具有类过氧化物酶活性的 AuPtAg 纳米酶可以改善肿瘤缺氧,显著提高 GOx 活性。结果,AuPtAg-GOx 与自我增强的光热能力和 PD-L1 抗体的结合可以进一步提高抗肿瘤疗效。基于 AuPtAg-GOx 的协同饥饿治疗、温和 PTT 和免疫治疗级联增强治疗策略可能是有效杀死癌细胞的有利工具。