Smart Nanoparticle-Based Platforms for Regulating Tumor Microenvironment and Cancer Immunotherapy

被引:32
|
作者
Cheng, Ruoyu [1 ,2 ,3 ]
Santos, Helder A. [1 ,2 ,3 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Biomed Engn, Ant Deusinglaan 1, NL-9713 AV Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, WJ Kolff Inst Biomed Engn & Mat Sci, Ant Deusinglaan 1, NL-9713 AV Groningen, Netherlands
[3] Univ Helsinki, Fac Pharm, Drug Res Program, Div Pharmaceut Chem & Technol, FI-00014 Helsinki, Finland
基金
芬兰科学院;
关键词
cancer immunotherapy; clinical translation; drug delivery; nanoparticles; tumor microenvironment; MHC CLASS-I; ENDOTHELIAL MARKERS; POLYMERIC MICELLES; BLACK PHOSPHORUS; CELLS; COLD;
D O I
10.1002/adhm.202202063
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Tumor development and metastasis are closely related to the tumor microenvironment (TME). Recently, several studies indicate that modulating TME can enhance cancer immunotherapy. Among various approaches to modulating TME, nanoparticles (NPs) with unique inherent advantages and smart modified characteristics are promising candidates in delivering drugs to cancer cells, amplifying the therapeutic effects, and leading to a cascade of immune responses. In this review, several smart NP-based platforms are briefly introduced, such as responsive NPs, targeting NPs, and the composition of TME, including dendritic cells, macrophages, fibroblasts, endothelial cells, myeloid-derived suppressor cells, and regulatory T cells. Moreover, the recent applications of smart NP-based platforms in regulating TME and cancer immunotherapy are briefly introduced. Last, the advantages and disadvantages of these smart NP-based platforms in potential clinical translation are discussed.
引用
收藏
页数:24
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