Biodegradable Hollow Mesoporous Silica Nanoparticles for Regulating Tumor Microenvironment and Enhancing Antitumor Efficiency

被引:153
作者
Kong, Miao [1 ,2 ]
Tang, Jiamin [3 ]
Qiao, Qi [1 ]
Wu, Tingting [1 ]
Qi, Yan [1 ]
Tan, Songwei [1 ,4 ]
Gao, Xueqin [1 ]
Zhang, Zhiping [1 ,4 ,5 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Sch Pharm, Wuhan 430030, Hubei, Peoples R China
[2] Sanmenxia Cent Hosp, Dept Pharm, Sanmenxia 472000, Peoples R China
[3] China Three Gorges Univ, Yichang 443002, Peoples R China
[4] Huazhong Univ Sci & Technol, Natl Engn Res Ctr Nanomed, Wuhan 430030, Hubei, Peoples R China
[5] Huazhong Univ Sci & Technol, Hubei Engn Res Ctr Novel Drug Delivery Syst, Wuhan 430030, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
nanoparticles; tumor microenvironment; immunosuppression; drug delivery; cancer treatment; TRANS-RETINOIC ACID; STEM-CELL DIFFERENTIATION; DRUG-DELIVERY SYSTEMS; EFFECTOR T-CELLS; CANCER-THERAPY; DEGRADATION BEHAVIOR; SUPPRESSOR-CELLS; INTERFERON-GAMMA; MYELOID CELLS; CO-DELIVERY;
D O I
10.7150/thno.19987
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
There is accumulating evidence that regulating tumor microenvironment plays a vital role in improving antitumor efficiency. Herein, to remodel tumor immune microenvironment and elicit synergistic antitumor effects, lipid-coated biodegradable hollow mesoporous silica nanoparticle (dHMLB) was constructed with co-encapsulation of all-trans retinoic acid (ATRA), doxorubicin (DOX) and interleukin-2 (IL-2) for chemo-immunotherapy. The nanoparticle-mediated combinational therapy provided a benign regulation on tumor microenvironment through activation of tumor infiltrating T lymphocytes and natural killer cells, promotion of cytokines secretion of IFN-gamma and IL-12, and down-regulation of immunosuppressive myeloid-derived suppressor cells, cytokine IL-10 and TGF-beta. ATRA/DOX/IL-2 co-loaded dHMLB demonstrated significant tumor growth and metastasis inhibition, and also exhibited favorable biodegradability and safety. This nanoplatform has great potential in developing a feasible strategy to remodel tumor immune microenvironment and achieve enhanced antitumor effect.
引用
收藏
页码:3276 / 3292
页数:17
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