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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
来源:
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.
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页码:5589 / 5598
页数:10
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