Anti-tumor immune response of dendritic cells derived from lymphoma cells transduced with recombinant adenovirus encoding human P53.
- Author:
Ze-Fa LIU
1
;
Hua TANG
;
Fei-Xue SONG
;
Peng-Yun ZENG
;
Ling-Ling YUE
;
Lian-Sheng ZHANG
Author Information
1. Department of Hematology, Xinghua Municipal People Hospital, Jiangsu Province, China.
- Publication Type:Journal Article
- MeSH:
Adenoviridae;
Cell Line, Tumor;
Dendritic Cells;
cytology;
immunology;
Genes, p53;
Genetic Vectors;
Humans;
Lymphocyte Activation;
Lymphocyte Culture Test, Mixed;
Lymphoma, Large B-Cell, Diffuse;
blood;
immunology;
Transfection
- From:
Journal of Experimental Hematology
2012;20(3):592-597
- CountryChina
- Language:Chinese
-
Abstract:
This study was aimed to investigate the immunological effect of modified dendritic cells (DC) which inducing cytotoxic T cells (CTL) against lymphoma cells. The DC were isolated from the lymph node and peripheral blood of patients with diffuse large B cell lymphoma (DLBCL). DC were transfected with recombinant adenovirus vector carrying human p53 gene (rAd-p53-DC). The expression of p53 gene was detected by flow cytometry. Western-blot was used to detect the expression of P53. ELISA was used to detect IL-12 level in supernatant. The mixed lymphocyte reaction (MLR) was used to detect the proliferative ability of auto-lymphocyte stimulated by DC. The lactate dehydrogenase (LDH) release test was used to determine the cytotoxicity of CTL. The results indicates that the expressions of DC surface molecule (except for CD1a) such as CD83, CD80, CD86 and HLA-DR were significantly higher in experiment group than that in control group and blank control group. The secretion of IL-12 in supernatant was higher in experiment group than that in control group. The autologous T lymphocyte proliferation and cytotoxic activity against the same kind of DLBL-cells increased in experiment group as compared with control group and blank control group (P < 0.05). The ability to stimulate T lymphocyte proliferation increased with the rising of the ratio of DC and T lymphocyte. However, there was statistically significant difference between rAd-p53-DC derived from Lymph node and peripheral blood (P < 0.05). It is concluded that rAd-p53-transfected DC can induce CTL response in vitro against lymphoma cells.
