Delivery of therapeutics with nanoparticles: what's new in cancer immunotherapy?

被引:64
作者
Fontana, Flavia [1 ]
Liu, Dongfei [1 ]
Hirvonen, Jouni [1 ]
Santos, Helder A. [1 ]
机构
[1] Univ Helsinki, Div Pharmaceut Chem & Technol, Fac Pharm, Helsinki, Finland
基金
芬兰科学院; 欧洲研究理事会;
关键词
MESOPOROUS SILICA NANOPARTICLES; T-CELL RESPONSE; POLY(PROPYLENE SULFIDE) NANOPARTICLES; ACETALATED DEXTRAN MICROPARTICLES; POTENT ANTITUMOR RESPONSES; TARGETING DENDRITIC CELLS; ENHANCED IMMUNE-RESPONSE; ANTIGEN-PRESENTING CELLS; DRUG-DELIVERY; IN-VIVO;
D O I
10.1002/wnan.1421
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The application of nanotechnology to the treatment of cancer or other diseases has been boosted during the last decades due to the possibility to precise deliver drugs where needed, enabling a decrease in the drug's side effects. Nanocarriers are particularly valuable for potentiating the simultaneous co-delivery of multiple drugs in the same particle for the treatment of heavily burdening diseases like cancer. Immunotherapy represents a new concept in the treatment of cancer and has shown outstanding results in patients treated with check-point inhibitors. Thereby, researchers are applying nanotechnology to cancer immunotherapy toward the development of nanocarriers for delivery of cancer vaccines and chemo-immunotherapies. Cancer nanovaccines can be envisioned as nanocarriers co-delivering antigens and adjuvants, molecules often presenting different physicochemical properties, in cancer therapy. A wide range of nanocarriers (e.g., polymeric, lipid-based and inorganic) allow the co-formulation of these molecules, or the delivery of chemo- and immune-therapeutics in the same system. Finally, there is a trend toward the use of biologically inspired and derived nanocarriers. In this review, we present the recent developments in the field of immunotherapy, describing the different systems proposed by categories: polymeric nanoparticles, lipid-based nanosystems, metallic and inorganic nanosystems and, finally, biologically inspired and derived nanovaccines. WIREs Nanomed Nanobiotechnol 2017, 9:e1421. doi: 10.1002/wnan.1421 For further resources related to this article, please visit the .
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页数:26
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