共 50 条
Emerging nanoparticle platforms for CpG oligonucleotide delivery
被引:9
|作者:
Li, Mingqiang
[1
]
Yao, Haochen
[2
]
Yi, Ke
[1
]
Lao, Yeh-Hsing
[3
]
Shao, Dan
[4
]
Tao, Yu
[1
]
机构:
[1] Sun Yat Sen Univ, Affiliated Hosp 3, Ctr Nanomed, Lab Biomat & Translat Med, Guangzhou 510630, Peoples R China
[2] First Hosp Jilin Univ, Gen Surg Ctr, Hepatobiliary & Pancreat Surg Dept, 1 Xinmin St, Changchun 130021, Jilin, Peoples R China
[3] SUNY Buffalo, Dept Pharmaceut Sci, Buffalo, NY 14214 USA
[4] South China Univ Technol, Sch Biomed Sci & Engn, Inst Life Sci, Guangzhou 510006, Guangdong, Peoples R China
基金:
中国国家自然科学基金;
关键词:
METAL-ORGANIC-FRAMEWORK;
MESOPOROUS SILICA NANOPARTICLES;
CALCIUM-PHOSPHATE NANOPARTICLES;
PLASMACYTOID DENDRITIC CELLS;
POLYMERIC HYBRID MICELLES;
ENHANCED IMMUNE-RESPONSE;
TOLL-LIKE RECEPTOR-9;
CO-DELIVERY;
IN-VIVO;
GOLD NANOPARTICLES;
D O I:
10.1039/d3bm01970e
中图分类号:
TB3 [工程材料学];
R318.08 [生物材料学];
学科分类号:
0805 ;
080501 ;
080502 ;
摘要:
Unmethylated cytosine-phosphate-guanine (CpG) oligodeoxynucleotides (ODNs), which were therapeutic DNA with high immunostimulatory activity, have been applied in widespread applications from basic research to clinics as therapeutic agents for cancer immunotherapy, viral infection, allergic diseases and asthma since their discovery in 1995. The major factors to consider for clinical translation using CpG motifs are the protection of CpG ODNs from DNase degradation and the delivery of CpG ODNs to the Toll-like receptor-9 expressed human B-cells and plasmacytoid dendritic cells. Therefore, great efforts have been devoted to the advances of efficient delivery systems for CpG ODNs. In this review, we outline new horizons and recent developments in this field, providing a comprehensive summary of the nanoparticle-based CpG delivery systems developed to improve the efficacy of CpG-mediated immune responses, including DNA nanostructures, inorganic nanoparticles, polymer nanoparticles, metal-organic-frameworks, lipid-based nanosystems, proteins and peptides, as well as exosomes and cell membrane nanoparticles. Moreover, future challenges in the establishment of CpG delivery systems for immunotherapeutic applications are discussed. We expect that the continuously growing interest in the development of CpG-based immunotherapy will certainly fuel the excitement and stimulation in medicine research. In this review, we provide a comprehensive summary of the nanoparticle-based CpG delivery systems developed to improve the efficacy of CpG-mediated immune responses.
引用
收藏
页码:2203 / 2228
页数:26
相关论文