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.
引用
收藏
页码:2127 / 2140
页数:14
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