CAS Key Laboratory for the Biological Effects of Nanomaterials and Nanosafety, Institute of High Energy Physics , Chinese Academy of Sciences , Beijing 100049 , China.
School of Pharmacy , Hebei University , Baoding 071002 , China.
ACS Appl Mater Interfaces. 2019 Apr 17;11(15):13964-13972. doi: 10.1021/acsami.9b01107. Epub 2019 Apr 8.
Nanomaterial-based tumor photothermal therapy (PTT) has attracted increasing attention and been a promising method for cancer treatment because of its low level of adverse effects and noninvasiveness. However, thermotherapy alone still cannot control tumor metastasis and recurrence. Here, we developed surface-functionalized modified copper sulfide nanoparticles (CuS NPs). CuS NPs can not only be used as photothermal mediators for tumor hyperthermia but can adsorb tumor antigens released during hyperthermia as an antigen-capturing agent to induce antitumor immune response. We selected maleimide polyethylene glycol-modified CuS NPs (CuS NPs-PEG-Mal) with stronger antigen adsorption capacity, in combination with an immune checkpoint blocker (anti-PD-L1) to evaluate the effect of hyperthermia, improving immunotherapy in a 4T1 breast cancer tumor model. The results showed that hyperthermia based on CuS NPs-PEG-Mal distinctly increased the levels of inflammatory cytokines in the serum, leading to a tumor immunogenic microenvironment. In cooperation with anti-PD-L1, PTT mediated by CuS NPs-PEG-Mal enhanced the number of tumor-infiltrating CD8 T cells and inhibited the growth in primary and distant tumor sites of the 4T1 tumor model. The therapeutic strategies provide a simple and effective treatment option for metastatic and recurrent tumors.
基于纳米材料的肿瘤光热疗法(PTT)因其低副作用和非侵入性而受到越来越多的关注,是一种很有前途的癌症治疗方法。然而,单纯的热疗仍然无法控制肿瘤的转移和复发。在这里,我们开发了表面功能化修饰的改性硫化铜纳米粒子(CuS NPs)。CuS NPs 不仅可以用作肿瘤高热的光热介质,还可以吸附热疗过程中释放的肿瘤抗原,作为抗原捕获剂,诱导抗肿瘤免疫反应。我们选择了具有更强抗原吸附能力的马来酰亚胺聚乙二醇修饰的 CuS NPs(CuS NPs-PEG-Mal),并结合免疫检查点抑制剂(抗 PD-L1),以评估在 4T1 乳腺癌肿瘤模型中高热诱导的免疫治疗效果。结果表明,基于 CuS NPs-PEG-Mal 的热疗显著提高了血清中炎症细胞因子的水平,导致肿瘤免疫原性微环境。与抗 PD-L1 联合应用时,CuS NPs-PEG-Mal 介导的 PTT 增强了肿瘤浸润性 CD8 T 细胞的数量,并抑制了 4T1 肿瘤模型的原发和远处肿瘤部位的生长。这些治疗策略为转移性和复发性肿瘤提供了一种简单有效的治疗选择。