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Efficacy and Mechanism of a Biomimetic Nanosystem Carrying Doxorubicin and an IDO Inhibitor for Treatment of Advanced Triple-Negative Breast Cancer
被引:7
作者:
Hu, Chuling
[1
]
Liu, Yan
[2
]
Cao, Wei
[3
]
Li, Na
[4
]
Gao, Shen
[5
]
Wang, Zhuo
[5
]
Gu, Fenfen
[2
]
机构:
[1] Jiaxing Univ, Affiliated Women & Childrens Hosp, Jiaxing Matern & Child Hlth Care Hosp, Dept Pharm, Jiaxing, Peoples R China
[2] Shanghai Jiao Tong Univ, Xinhua Hosp, Sch Med, Dept Clin Pharm, Shanghai, Peoples R China
[3] Tongji Univ, Shanghai Peoples Hosp 4, Sch Med, Dept Neurovasc Dis, Shanghai, Peoples R China
[4] Jiaxing Univ, Jiaxing Matern & Child Hlth Care Hosp, Dept Pathol, Affiliated Women & Childrens Hosp, Jiaxing, Peoples R China
[5] Second Mil Med Univ, Changhai Hosp, Dept Pharm, Shanghai, Peoples R China
关键词:
immunogenic cell death;
doxorubicin;
bionic nanoparticle;
IDO1;
inhibitor;
triple-negative breast cancer;
IMMUNOGENIC CELL-DEATH;
IMMUNOTHERAPY;
NANOPARTICLES;
CHECKPOINT;
TUMOR;
D O I:
10.2147/IJN.S440332
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Introduction: Chemotherapy is still the treatment of choice for advanced triple-negative breast cancer. Chemotherapy combined with immunotherapy is being tried in patients with triple-negative breast cancer. As a kind of "cold tumor", triple-negative breast cancer has a bottleneck in immunotherapy. Indoleamine 2, 3-dioxygenase-1 inhibitors can reverse the immunosuppressive state and enhance the immune response.Methods: In this study, mesoporous silica nanoparticles were coated with the chemotherapeutic drug doxorubicin and indoleamine 2, 3-dioxygenase 1 inhibitor 1-Methyl-DL-tryptophan (1-MT), and then encapsulate the surfaces of a triple-negative breast cancer cell membrane to construct the tumor dual-targeted delivery system CDIMSN for chemotherapy and immunotherapy, and to investigate the immunogenic death effect of CDIMSN.Results and discussion: The CDIMSN could target the tumor microenvironment. Doxorubicin induced tumor immunogenic death, while 1-MT reversed immunosuppression. In vivo findings showed that the tumor size in the CDIMSN group was 2.66-fold and 1.56fold smaller than that in DOX and DIMSN groups, respectively. CDIMSN group was better than naked DIMSN in stimulating CD8+T cells, CD4+T cells and promoting Dendritic Cells(DC) maturation. In addition, blood analysis, biochemical analysis and Hematoxylin staining analysis of mice showed that the bionic nanoparticles had good biological safety.
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页码:507 / 526
页数:20
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