Abstract
Improving vaccine immunogenicity remains a major challenge in the fight against developing country diseases like malaria and AIDS. We describe a novel strategy to identify new DNA vaccine adjuvants. We have screened components of the Toll-like receptor signalling pathways for their ability to activate pro-inflammatory target genes in transient transfection assays and assessed in vivo adjuvant activity by expressing the activators from the DNA backbone of vaccines. We find that a robust increase in the immune response necessitates co-expression of two activators. Accordingly, the combination of tak1 and tram elicits synergistic reporter activation in transient transfection assays. In a mouse model this combination, but not the individual molecules, induced approximately twofold increases in CD8+ T-cell immune responses. These results indicate that optimal immunogenicity may require activation of distinct innate immune signalling pathways. Thus this strategy offers a novel route to the discovery of a new generation of adjuvants. © 2009 Elsevier Ltd. All rights reserved.
Author supplied keywords
Cite
CITATION STYLE
Larsen, K. C., Spencer, A. J., Goodman, A. L., Gilchrist, A., Furze, J., Rollier, C. S., … Wyllie, D. H. (2009). Expression of tak1 and tram induces synergistic pro-inflammatory signalling and adjuvants DNA vaccines. Vaccine, 27(41), 5589–5598. https://doi.org/10.1016/j.vaccine.2009.07.025
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.