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Figure 1. Structures and IUPAC names of DOTAP, DC-Chol and DDA.
(Figure omitted. See article PDF.)
Figure 2. Dimethyldioctadecylammonium (DDA) liposomes enhance uptake and presentation of antigen by dendritic cells. (A) Antigen-loaded DDA liposomes associate with antigen-presenting cells thus enhancing the uptake of antigen. (B) This can be visualized by confocal microscopy: antigen is shown in green, the actin filaments of a dendritic cell in red. It is not yet known whether the antigen is internalized alone (as depicted) or together with the liposomes. (B-C) The enhanced uptake leads to enhanced presentation of antigen by the dendritic cells. This results in increased proliferation of antigen-specific T cells and their subsequent release of IFN-γ as demonstrated by incorporation of radioactively labeled thymidine and detection of IFN-γ by ELISA after 2 days of coculture. Previously published in [47]. Ag: Antigen.
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Figure 3. Incorporation of glycolipids into dimethyldioctadecylammonium (DDA) liposomes can stabilize the particle size distribution and avoid aggregation. (A) The particle size of liposomes formed by DDA, DDA/TDB and DDA/LAcCer. Furthermore, (B) shows the synergistic effect between DDA and TDB, on their own generating a very low immune response, but together generating a strong immune response. However, not all glycolipids obtain as powerful an adjuvant effect upon incorporation into the DDA liposomes as TDB; this is illustrated with LacCer showing antigen-specific IFN-γ levels in blood (pg/ml) after three immunizations with Ag85B-ESAT-6. *After 28 days, DDA is too aggregated to measure the particle size. LacCer: :actocylceramide; TDB: Trehalose 6,6´-dibehenate.
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Figure 4. Immune responses generated by DDA/TDB liposomes and Al(OH)3 . (A) Dimethyldioctadecylammonium/trehalose 6,6´-dibehenate (DDA/TDB) induces high levels of the Th1 cytokine IFN-γ and (B) low levels of the Th2 cytokine IL-5, which is diametrical opposite to the induction obtained by Al(OH)3 . (C) DDA/TDB induces IgG1 levels similar to Al(OH)3 , but (D) higher levels of IgG2b . Previously published in [31]
(Figure omitted. See article PDF.)
Figure 5. Formulation of immunomodulators together with cationic liposomes is a promising method to enhance and modulate the immune response in a desirable direction and can be used when designing tailor-made adjuvants for specific disease targets. CTL: Cytotoxic T lymphocyte; MDP: Muramyl dipeptide; MPL: Monophosphoryl...





