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免疫刺激纳米药物与检查点阻断免疫疗法协同作用,以根除结直肠肿瘤。

Immunostimulatory nanomedicines synergize with checkpoint blockade immunotherapy to eradicate colorectal tumors.

机构信息

Department of Chemistry, The University of Chicago, 929 E 57th St, Chicago, IL, 60637, USA.

Cancer Research Institute, Guangdong Provincial Key Laboratory of Cancer Immunotherapy, School of Basic Medical Sciences, Southern Medical University, 510515, Guangzhou, PR China.

出版信息

Nat Commun. 2019 Apr 23;10(1):1899. doi: 10.1038/s41467-019-09221-x.

Abstract

Nanoparticles can potentially stimulate tumour microenvironments to elicit antitumour immunity. Herein, we demonstrate effective immunotherapy of colorectal cancer via systemic delivery of an immunostimulatory chemotherapeutic combination in nanoscale coordination polymer (NCP) core-shell particles. Oxaliplatin and dihydroartemesinin have contrasting physicochemical properties but strong synergy in reactive oxygen species (ROS) generation and anticancer activity. The combined ROS generation is harnessed for immune activation to synergize with an anti-PD-L1 antibody for the treatment of murine colorectal cancer tumours. The favourable biodistribution and tumour uptake of NCPs and the absence of peripheral neuropathy allow for repeated dosing to afford 100% tumour eradication. The involvement of innate and adaptive immune systems elicit strong and long lasting antitumour immunity which prevents tumour formation when cured mice are challenged with cancer cells. The intrinsically biodegradable, well tolerated, and systemically available immunostimulatory NCP promises to enter clinical testing as an immunotherapy against colorectal cancer.

摘要

纳米颗粒有可能刺激肿瘤微环境,引发抗肿瘤免疫。在此,我们通过在纳米级配位聚合物(NCP)核壳粒子中系统递送来展示结直肠癌的有效免疫治疗。奥沙利铂和青蒿琥酯具有相反的物理化学性质,但在活性氧(ROS)生成和抗癌活性方面具有很强的协同作用。联合产生的 ROS 被用于免疫激活,与抗 PD-L1 抗体协同作用,用于治疗小鼠结直肠肿瘤。NCPs 的有利的生物分布和肿瘤摄取以及没有周围神经病变允许重复给药,以实现 100%的肿瘤消除。先天和适应性免疫系统的参与引发了强烈和持久的抗肿瘤免疫,当治愈的小鼠受到癌细胞的挑战时,可防止肿瘤形成。固有可生物降解、耐受性良好且可系统获得的免疫刺激 NCP 有望作为结直肠癌的免疫疗法进入临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27bd/6478897/10565f6585d7/41467_2019_9221_Fig1_HTML.jpg

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