CpG motifs are efficient adjuvants for DNA cancer vaccines

被引:49
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
相关论文
共 58 条
  • [1] Ahmad-Nejad P, 2002, EUR J IMMUNOL, V32, P1958, DOI 10.1002/1521-4141(200207)32:7<1958::AID-IMMU1958>3.0.CO
  • [2] 2-U
  • [3] Role of plasmacytoid dendritic cells in immunity and tolerance after allogeneic hematopoietic stem cell transplantation
    Arpinati, M
    Chirumbolo, G
    Urbini, B
    Perrone, G
    Rondelli, D
    Anasetti, C
    [J]. TRANSPLANT IMMUNOLOGY, 2003, 11 (3-4) : 345 - 356
  • [4] Baines J, 2003, CLIN CANCER RES, V9, P2693
  • [5] Divergent therapeutic and immunologic effects of oligodeoxynucleotides with distinct CpG motifs
    Ballas, ZK
    Krieg, AM
    Warren, T
    Rasmussen, W
    Davis, HL
    Waldschmidt, M
    Weiner, GJ
    [J]. JOURNAL OF IMMUNOLOGY, 2001, 167 (09) : 4878 - 4886
  • [6] Immunostimulatory CpG oligonucleotides enhance the immune response of anti-idiotype vaccine that mimics carcinoembryonic antigen
    Baral, RN
    Saba, A
    Chatterjee, SK
    Foon, KA
    Krieg, AM
    Weiner, GJ
    Bhattacharya-Chatterjee, M
    [J]. CANCER IMMUNOLOGY IMMUNOTHERAPY, 2003, 52 (05) : 317 - 327
  • [7] Bacterial CpG-DNA triggers activation and maturation of human CD11c-, CD123+ dendritic cells
    Bauer, M
    Redecke, V
    Ellwart, JW
    Scherer, B
    Kremer, JP
    Wagner, H
    Lipford, GB
    [J]. JOURNAL OF IMMUNOLOGY, 2001, 166 (08) : 5000 - 5007
  • [8] Human TLR9 confers responsiveness to bacterial DNA via species-specific CpG motif recognition
    Bauer, S
    Kirschning, CJ
    Häcker, H
    Redecke, V
    Hausmann, S
    Akira, S
    Wagner, H
    Lipford, GB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (16) : 9237 - 9242
  • [9] Cellular cytotoxic response induced by DNA vaccination in HIV-1-infected patients
    Calarota, S
    Bratt, G
    Nordlund, S
    Hinkula, J
    Leandersson, AC
    Sandström, E
    Wahren, B
    [J]. LANCET, 1998, 351 (9112) : 1320 - 1325
  • [10] Carpentier AF, 2000, CLIN CANCER RES, V6, P2469