Expression of tak1 and tram induces synergistic pro-inflammatory signalling and adjuvants DNA vaccines

被引:18
作者
Larsen, Karen Colbjorn [1 ]
Spencer, Alexandra J. [1 ]
Goodman, Anna L. [1 ]
Gilchrist, Ashley [2 ]
Furze, Julie [1 ]
Rollier, Christine S. [1 ]
Kiss-Toth, Endre [3 ]
Gilbert, Sarah C. [1 ]
Bregu, Migena [1 ]
Soilleux, Elizabeth J. [2 ]
Hill, Adrian V. S. [1 ]
Wyllie, David H. [1 ]
机构
[1] Univ Oxford, Jenner Inst, Oxford OX3 7DQ, England
[2] John Radcliffe Hosp, Dept Cellular Pathol, Oxford OX3 9DU, England
[3] Univ Sheffield, Cardiovasc Res Unit, Sheffield S10 2RX, S Yorkshire, England
基金
美国国家卫生研究院; 英国惠康基金;
关键词
DNA vaccine; Adjuvant; tak1; tram; cxcl2; NF-KAPPA-B; T-CELL RESPONSES; IMMUNE-RESPONSES; PLASMID DNA; NEUTRALIZING ANTIBODY; ADAPTER MOLECULE; GENE-EXPRESSION; HEALTHY-ADULTS; KINASE CASCADE; PRIME-BOOST;
D O I
10.1016/j.vaccine.2009.07.025
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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. (c) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5589 / 5598
页数:10
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