Tumor immune microenvironment modulation-based drug delivery strategies for cancer immunotherapy

被引:54
作者
Han, Shuyan [1 ]
Huang, Keqing [1 ]
Gu, Zhipeng [2 ]
Wu, Jun [1 ]
机构
[1] Sun Yat Sen Univ, Sch Biomed Engn, Key Lab Sensing Technol & Biomed Instrument Guang, Guangzhou 510006, Peoples R China
[2] Sichuan Univ, Coll Polymer Sci & Engn, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R China
关键词
REGULATORY T-CELLS; LYSOSOMAL ACID LIPASE; DENDRITIC CELLS; IN-VIVO; CHECKPOINT INHIBITORS; MAST-CELLS; NANOPARTICLE DELIVERY; LYMPHOID STRUCTURES; ONCOLYTIC VIRUSES; ANTIBODY THERAPY;
D O I
10.1039/c9nr08086d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The past years have witnessed promising clinical feedback for anti-cancer immunotherapies, which have become one of the hot research topics; however, they are limited by poor delivery kinetics, narrow patient response profiles, and systemic side effects. To the best of our knowledge, the development of cancer is highly associated with the immune system, especially the tumor immune microenvironment (TIME). Based on the comprehensive understanding of the complexity and diversity of TIME, drug delivery strategies focused on the modulation of TIME can be of great significance for directing and improving cancer immunotherapy. This review highlights the TIME modulation in cancer immunotherapy and summarizes the versatile TIME modulation-based cancer immunotherapeutic strategies, medicative principles and accessory biotechniques for further clinical transformation. Remarkably, the recent advances of cancer immunotherapeutic drug delivery systems and future prospects of TIME modulation-based drug delivery systems for much more controlled and precise cancer immunotherapy will be emphatically discussed.
引用
收藏
页码:413 / 436
页数:24
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