共 27 条
Surface-Engineered Monocyte Immunotherapy Combined Graphene Quantum Dots Effective Against Solid Tumor Targets
被引:8
|作者:
Xia, Qing
[1
]
Tang, Yue
[1
]
Li, Wang
[1
]
Liang, Tingting
[1
]
Zhou, Yue
[1
]
Liu, Jun
[1
]
Liu, Feila
[1
]
机构:
[1] Chongqing Univ Technol, Sch Pharm & Bioengn, Chongqing, Peoples R China
来源:
关键词:
solid tumor;
surface-engineered monocyte;
GQDs;
miR155;
immunotherapy;
MICRORNA DELIVERY;
PROTECTIVE ROLE;
T-CELLS;
MACROPHAGES;
NANOPARTICLES;
INJURY;
DRUG;
GROWTH;
D O I:
10.2147/IJN.S404486
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Introduction: The immunosuppressive tumor microenvironment (TME) of solid tumors inhibits most drug delivery system-based nanomaterials from achieving deep penetration in tumor tissue and interferes with T cell activity in terms of differentiation and exhaustion, which is becoming a critical therapy hurdle for solid tumors. Therefore, developing a therapeutic strategy with abilities of rapid establishment of tumor-targeted cells, elimination of immune obstacles, and enhanced active immunization is very important, while is still a big challenge. Methods: A new strategy was explored to enhance immune therapy via the conjugation of microRNA155 (miR) to the surface of therapeutic monocyte with graphene quantum dots (GQDs). Results: TME was reversed using surface-engineered monocyte immunotherapy via reprogramming pro-tumoral M2 TAMs into antitumor M1, and thus tumor elimination was dramatically enhanced. Conclusion: Such a surface-engineered monocyte immunotherapy has been demonstrated to be well tolerated to intravenous administration and bio-compatible, showing the potential to be extended for the solid tumor treatment.
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页码:2127 / 2140
页数:14
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