The immunostimulatory effects of retinoblastoma cell supernatant on dendritic cells.
10.1007/s13238-014-0029-0
- Author:
Juan MA
1
;
Huamin HAN
;
Li MA
;
Changzhen LIU
;
Xin XUE
;
Pan MA
;
Xiaomei LI
;
Hua TAO
Author Information
1. CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100101, China, majuan96@sina.com.
- Publication Type:Journal Article
- MeSH:
B7-1 Antigen;
metabolism;
B7-2 Antigen;
metabolism;
Cell Line, Tumor;
Cell Proliferation;
drug effects;
Culture Media, Conditioned;
pharmacology;
Cytokines;
metabolism;
Dendritic Cells;
drug effects;
immunology;
metabolism;
Humans;
Lipopolysaccharides;
toxicity;
Retinal Neoplasms;
metabolism;
pathology;
Retinoblastoma;
metabolism;
pathology;
T-Lymphocytes;
cytology;
immunology;
metabolism;
Tumor Necrosis Factor-alpha;
pharmacology
- From:
Protein & Cell
2014;5(4):307-316
- CountryChina
- Language:English
-
Abstract:
Dendritic cells (DCs) are crucial for the induction and maintenance of tumor-specific immune responses. Studies have shown that tumor-associated DCs are immunosuppressed in some human tumors. However, phenotype and function of DCs in retinoblastoma (RB) remain unclear. RB cell supernatant (RBcs) was used to treat DCs in vitro to explore the effect of RB cells on DCs. DCs were generated from peripheral blood mononuclear cells of healthy donors. On day 5 of culture, DCs were treated with RBcs for 24 h, and then purified using magnetic beads. The maturation of DCs was induced by TNF-α or LPS. After treatment with RBcs, expression of co-stimulatory molecules CD80 and CD86 was elevated in DCs, accompanied by increased production of IL-12p70, TNF-α, IL-6, IL-1β, and IL-8 but decreased production of IL-10. RBcs neither inhibited DC maturation nor promoted DC apoptosis. Moreover, RBcs-exposed DCs stimulated allogenetic T cell proliferation and T cell-derived cytokine production. These results indicate that RBcs can improve DCs' antigen presenting function and capability to activate T cells, suggesting that RB cells may have an immunostimulatory effect on DCs, and DC-based immunotherapy may be adopted in the treatment of RB.
