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基于纳米颗粒的光热疗法和抗 PD-1 检查点抑制联合诱导小鼠抗肿瘤免疫。

Induction of antitumor immunity in mice by the combination of nanoparticle-based photothermolysis and anti-PD-1 checkpoint inhibition.

机构信息

Department of Cancer Systems Imaging, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

出版信息

Nanomedicine. 2020 Apr;25:102169. doi: 10.1016/j.nano.2020.102169. Epub 2020 Feb 12.

Abstract

Generation of durable tumor-specific immune response without isolation and expansion of dendritic cells or T cells ex vivo remains a challenge. In this study, we investigated the impact of nanoparticle-mediated photothermolysis in combination with checkpoint inhibition on the induction of systemic antitumor immunity. Photothermolysis based on near-infrared light-absorbing copper sulfide nanoparticles and 15-ns laser pulses combined with the immune checkpoint inhibitor anti-PD-1 antibody (αPD-1) increased tumor infiltration by antigen-presenting cells and CD8-positive T lymphocytes in the B16-OVA mouse model. Moreover, combined photothermolysis, polymeric conjugate of the Toll-like receptor 9 agonist CpG, and αPD-1 significantly prolonged mouse survival after re-inoculation of tumor cells at a distant site compared to individual treatments alone in the poorly immunogenic syngeneic ID8-ip1-Luc ovarian tumor model. Thus, photothermolysis is a promising interventional technique that synergizes with Toll-like receptor 9 agonists and immune checkpoint inhibitors to enhance the abscopal effect in tumors.

摘要

在不分离和扩增树突状细胞或 T 细胞的情况下产生持久的肿瘤特异性免疫反应仍然是一个挑战。在这项研究中,我们研究了纳米颗粒介导的光热疗法联合检查点抑制对诱导全身抗肿瘤免疫的影响。基于近红外光吸收的硫化铜纳米颗粒和 15 纳秒激光脉冲的光热疗法与免疫检查点抑制剂抗 PD-1 抗体(αPD-1)联合使用,增加了 B16-OVA 小鼠模型中抗原呈递细胞和 CD8 阳性 T 淋巴细胞的肿瘤浸润。此外,与单独使用单一疗法相比,联合光热疗法、Toll 样受体 9 激动剂 CpG 的聚合物缀合物和 αPD-1 在重新接种远处肿瘤细胞后显著延长了 ID8-ip1-Luc 卵巢肿瘤模型中同种异体小鼠的存活时间。因此,光热疗法是一种很有前途的介入技术,可与 Toll 样受体 9 激动剂和免疫检查点抑制剂协同作用,增强肿瘤的远隔效应。

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