CpG motifs are efficient adjuvants for DNA cancer vaccines

被引:50
|
作者
Schneeberger, A
Wagner, C [1 ]
Zemann, A
Lührs, P
Kutil, R
Goos, M
Stingl, G
Wagner, SN
机构
[1] Med Univ Vienna, Dept Dermatol, Div Immunol Allergy & Infect Dis, Vienna, Austria
[2] Austrian Acad Sci, CeMM Res Ctr Mol Med, A-1010 Vienna, Austria
[3] Univ Duisburg Essen, Dept Dermatol, Duisburg, Germany
关键词
CpG motifs; CTL; melanoma; pDNA; tumor immunity;
D O I
10.1111/j.0022-202X.2004.23208.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
DNA vaccines can induce impressive specific cellular immune response (IR) when taking advantage of their recognition as pathogen-associated molecular patterns (PAMP) through Toll-like receptors (TLR) expressed on/in cells of the innate immune system. Among the many types of PAMP, immunostimulatory DNA, so-called CpG motifs, was shown to interact specifically with TLR9, which is expressed in plasmacytoid dendritic cells (pDC), a key regulatory cell for the activation of innate and adaptive IR. We now report that CpG motifs, when introduced into the backbone, are a useful adjuvant for plasmid-based DNA (pDNA) vaccines to induce melanoma antigen-specific protective T cell responses in the Cloudman M3/DBA/2 model. The CpG-enriched pDNA vaccine induced protection against subsequent challenge with melanoma cells at significantly higher levels than its parental unmodified vector. Preferential induction of an antigen-specific, protective T cell response could be demonstrated by (i) induction of antigen-dependent tumor cell protection, (ii) complete loss of protection by in vivo CD4(+)/CD8(+)T cell- but not NK cell-depletion, and (iii) the detection of antigen-specific T cell responses but not of relevant NK cell activity in vitro. These results demonstrate that employing PAMP in pDNA vaccines improves the induction of protective, antigen-specific, T cell-mediated IR.
引用
收藏
页码:371 / 379
页数:9
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