Nanomedicines modulating myeloid-derived suppressor cells for improving cancer immunotherapy

被引:22
|
作者
Dai, Xinghang [1 ,2 ]
Ren, Long [1 ]
Liu, Mengxi [1 ,2 ]
Cai, Hao [1 ]
Zhang, Hu [4 ]
Gong, Qiyong [1 ,2 ,3 ]
Gu, Zhongwei [1 ]
Luo, Kui [1 ]
机构
[1] Sichuan Univ, West China Hosp, Huaxi MR Res Ctr HMRRC, Natl Clin Res Ctr Geriatr,Dept Radiol,Funct & Mol, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Sch Med, Chengdu 610041, Peoples R China
[3] Chinese Acad Med Sci, Res Unit Psychoradiol, Chengdu 610041, Peoples R China
[4] Keck Grad Inst, Amgen Bioproc Ctr, Claremont, CA 91711 USA
基金
中国国家自然科学基金;
关键词
Cancer immunotherapy; Myeloid-derived suppressor cells; Nanomedicine; Tumor microenvironment; Drug delivery; Antitumor immunity; IMMUNE-CHECKPOINT BLOCKADE; ENHANCES VACCINE THERAPY; TUMOR MICROENVIRONMENT; URSOLIC-ACID; ANTITUMOR IMMUNITY; MULTILAMELLAR LIPOSOMES; PHOTODYNAMIC THERAPY; PREMETASTATIC NICHE; POLYMERIC MICELLES; TARGETED DELIVERY;
D O I
10.1016/j.nantod.2021.101163
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Great success in immunotherapy has revolutionized clinical cancer treatments. However, the response rate and overall survival rate remain unsatisfactory. As one of the immunological hallmarks of cancer, myeloidderived suppressor cells (MDSCs) induce strong immunosuppression, which leads to great hindrance for immunotherapy of cancer. Thus, MDSCs have been explored as an important immunotherapeutic target to enhance anticancer responses. Nanomedicines have been developed to target MDSCs to improve the immunotherapeutic efficacy owing to their ability of reversing immunosuppressive tumors into immunoresponsive ones. In this review, we describe the function of MDSCs in the tumor microenvironment and the immunosuppressive pathways that inhibit T cell functions. Additionally, recent developments in various nanoparticulate platforms, including nanocapsules, micelles, liposomes, mineralized/metallic nanoparticles and hydrogels, affecting through different pathways and functions of MDSCs as immunomodulatory agents are discussed and highlighted. These nanomedicines have been demonstrated with improved therapeutic efficacies by modulating MDSCs, and they have great potential of translation to clinical application in cancer nano-immunotherapy. (c) 2021 Elsevier Ltd. All rights reserved.
引用
收藏
页数:23
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