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Journal of Southern Medical University ; (12): 1893-1895, 2009.
Article in Chinese | WPRIM | ID: wpr-336057

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate the immunostimulatory capacity of human peripheral blood dendritic cells (DCs) with Her2/neu gene transfection mediated by adeno-associated virus.</p><p><b>METHODS</b>The HLA genotypes of the breast cancer cells SK-BR-3 and MCF7 were determined, and the mononuclear cells from healthy donors with matching HLA genotype were isolated by Ficoll-Hypaque density gradient separation. The isolated cells were divided into two groups with or without transfection with the recombinant virus harboring Her2/neu gene. The cells were cultured for 7 days in RPMI 1640 medium supplemented with 10% AB human serum, GM-CSF, interleukin-4 (IL-4) and tumor necrosis factor-alpha (TNF-alpha). The mature DCs were then harvested from the cell culture and their phenotypes were identified using flow cytometry. MTT assay was employed to examine the specific killing activity of the T cells induced by the DCs.</p><p><b>RESULTS</b>The DCs transfected with the recombinant adeno-associated virus expressed CD1a, CD86 and CD83 at the rate of 98.10%, 99.42%, and 84.59%, and those without the viral transfection expressed the markers at the rate 92.69%, 98.07%, and 82.72%, respectively, showing no obvious differences in the phenotypes of the two DCs. The transfected DCs, however, showed markedly higher expression rates of CD40 and CD80 than the non-transfected DCs (61.02% vs 36.19%, and 97.61% vs 55.5%, respectively). The DCs, irrespective of the transfection, showed comparable capacities in stimulating T cell proliferation. The transfected DCs exhibited the capacity of inducing the T cells to specifically kill the target tumor cells, with the highest killing rate of (39.7-/+7.2)%.</p><p><b>CONCLUSION</b>The immunostimulatory capacity of human peripheral blood DCs are enhanced by Her2/neu gene transfection mediated by adeno-associated virus.</p>


Subject(s)
Humans , Breast Neoplasms , Pathology , Cell Line, Tumor , Cells, Cultured , Dendritic Cells , Cell Biology , Allergy and Immunology , Metabolism , Dependovirus , Genetics , Metabolism , Genes, erbB-2 , Genetics , Genetic Vectors , Granulocyte-Macrophage Colony-Stimulating Factor , Pharmacology , Leukocytes, Mononuclear , Cell Biology , Receptor, ErbB-2 , Genetics , Recombinant Proteins , Genetics , Allergy and Immunology , Metabolism , Transfection
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