This article is part of the supplement: AIDS Vaccine 2009
Poster presentation
P19-10. Induction of dendritic cell maturation by a liposomally-delivered multivalent HIV vaccine
1 Variation Biotechnologies Inc., 1740 Woodroffe Ave, Building 400, Ottawa, ON, K2G 3R8, Canada
2 Department of Biochemistry, Microbiology and Immunology, University of Ottawa, and Infectious Disease and Vaccine Research Center, Children's Hospital of Eastern Ontario Research Institute, 401 Smyth, Ottawa, ON, K1H 8L1, Canada
3 Department of Pathology and Laboratory Medicine, University of Ottawa, 451 Smyth, Ottawa, ON, K1H 8M5, Canada
4 Department of Medical Microbiology and Immunology, Davis School of Medicine, University of California, Davis, CA 95616, USA
Retrovirology 2009, 6(Suppl 3):P330 doi:10.1186/1742-4690-6-S3-P330
The electronic version of this article is the complete one and can be found online at: http://www.retrovirology.com/content/6/S3/P330
| Published: | 22 October 2009 |
© 2009 Azizi et al; licensee BioMed Central Ltd.
Background
We have previously developed an innovative vaccine based on the genetic mutability and diversity of variable HIV-1 epitopes. This polyvalent peptide vaccine has been shown to induce a broadly reactive peripheral immune response in mice and macaques (Azizi A, J. Immunol, 2008). Our group recently developed a lipid-based vesicle as an oral vaccine delivery system for the induction of mucosal immunity within mucosal tissues. In this study, we take advantage of this technology to entrap our HIV-1 vaccine into this lipid-based vesicle. We then evaluated the ability of our vaccine formulations to induce maturation of mouse dendritic cells. In vitro experiments have shown our liposomally-delivered candidate vaccine to be effective in inducing the maturation of mouse dendritic cells, as demonstrated by increased cell surface MHCII and CD86 expression.
Methods
Mice were sacrificed and bone marrow from femur, tibia and humerus was collected. Marrow cells were then cultured in the presence of IL-4 and GM-CSF for 5 days before being loaded with antigen to induce maturation. The presence of cell surface markers related to dendritic cell maturation was then evaluated by flow cytometry.
Results
Stimulation of immature bone marrow-derived murine dendritic cells with liposomally-delivered HIV peptides induces maturation of these cells, as determined by increased expression of cell-surface markers MHCII and CD86.
Conclusion
Our data indicate that the incorporation of multiple HIV-1 epitopes into a lipid-based delivery system is effective in inducing the maturation of murine dendritic cells. Our findings suggest that a liposomal-based delivery system may act as an effective delivery vehicle.