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      DiC14-amidine cationic liposomes stimulate myeloid dendritic cells through Toll-like receptor 4.

      European Journal of Immunology
      Adaptor Proteins, Vesicular Transport, genetics, Adjuvants, Immunologic, administration & dosage, pharmacology, Amidines, Animals, Cell Line, Cytokines, metabolism, Dendritic Cells, drug effects, Female, Humans, Interleukin-12 Subunit p40, Lymphocyte Antigen 96, Mice, Mice, Inbred BALB C, Mice, Inbred C57BL, Mice, Knockout, Mice, Mutant Strains, Mitogen-Activated Protein Kinases, Myeloid Cells, cytology, Myeloid Differentiation Factor 88, NF-kappa B, Phosphorylation, Toll-Like Receptor 4, agonists, Toll-Like Receptors, Transfection, Tumor Necrosis Factor-alpha

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          Abstract

          DiC14-amidine cationic liposomes were recently shown to promote Th1 responses when mixed with allergen. To further define the mode of action of diC14-amidine as potential vaccine adjuvant, we characterized its effects on mouse and human myeloid dendritic cells (DC). First, we observed that, as compared with two other cationic liposomes, only diC14-amidine liposomes induced the production of IL-12p40 and TNF-alpha by mouse bone marrow-derived DC. DiC14-amidine liposomes also activated human DC, as shown by synthesis of IL-12p40 and TNF-alpha, accumulation of IL-6, IFN-beta and CXCL10 mRNA, and up-regulation of membrane expression of CD80 and CD86. DC stimulation by diC14-amidine liposomes was associated with activation of NF-kappaB, ERK1/2, JNK and p38 MAP kinases. Finally, we demonstrated in mouse and human cells that diC14-amidine liposomes use Toll-like receptor 4 to elicit both MyD88-dependent and Toll/IL-1R-containing adaptor inducing interferon IFN-beta (TRIF)-dependent responses.

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