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• W2037498110 startingPage "278" @default.
• W2037498110 abstract "Monocyte-derived dendritic cells (mDC), the most frequently applied DC subset in clinical studies, which can be obtained easily from peripheral blood monocytes after incubation with GM-CSF and IL-4, have not been clearly demonstrated to be activated by CpG oligodeoxynucleotides (ODN). The development of novel molecular strategies - such as the use of CpG-ODN - to increase immunological functions and thus improve the therapeutic efficiency of mDC vaccines in the treatment of malignant diseases is highly desirable. CpG-ODN need to be internalized into specific intracellular compartments to be active. Therefore, we applied electroporation and lipofection and compared these techniques with incubation to overcome possible defects in localization. Conditions of CpG-ODN transfection of these cells were optimized using fluorescein-marked ODN 2216. We were able to achieve high transfection efficiencies with various methods of delivery. However, we did not observe increased expression of maturation-associated and functionally relevant surface antigens (CD14, HLA-DR, CD40, CD83, CD80 and CD86), significant secretion of IL-12 and IFN-alpha in culture supernatant, or enhanced antitumour activation of cytokine-induced killer cells. In conclusion, our results show that non-viral transfection of CpG-ODN is not sufficient to overcome resistance of mDC to CpG activation." @default.
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• W2037498110 date "2005-06-01" @default.
• W2037498110 modified "2023-09-26" @default.
• W2037498110 title "Transfection of human monocyte‐derived dendritic cells with CpG oligonucleotides" @default.
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• W2037498110 doi "https://doi.org/10.1111/j.1440-1711.2005.01328.x" @default.
• W2037498110 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/15877606" @default.
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