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
相关论文
共 60 条
[1]   Combined TLR and CD40 triggering induces potent CD8+ T cell expansion with variable dependence on type I IFN [J].
Ahonen, CL ;
Doxsee, CL ;
McGurran, SM ;
Riter, TR ;
Wade, WF ;
Barth, RJ ;
Vasilakos, JP ;
Noelle, RJ ;
Kedl, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 199 (06) :775-784
[2]   Activation of NF-κB by the intracellular expression of NF-κB-inducing kinase acts as a powerful vaccine adjuvant [J].
Andreakos, E. ;
Williams, R. O. ;
Wales, J. ;
Foxwell, B. M. ;
Feldmann, M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (39) :14459-14464
[3]   Activation of innate immunity, inflammation, and potentiation of DNA vaccination through mammalian expression of the TLR5 agonist flagellin [J].
Applequist, SE ;
Rollman, E ;
Wareing, MA ;
Lidén, M ;
Rozell, B ;
Hinkula, J ;
Ljunggren, HG .
JOURNAL OF IMMUNOLOGY, 2005, 175 (06) :3882-3891
[4]   The HIV-1 matrix protein p 17 can be efficiently delivered by intranasal route in mice using the TLR 2/6 agonist MALP-2 as mucosal adjuvant [J].
Becker, Pablo D. ;
Fiorentini, Simona ;
Link, Claudia ;
Tosti, Giorgio ;
Ebensen, Thomas ;
Caruso, Arnaldo ;
Guzman, Carlos A. .
VACCINE, 2006, 24 (25) :5269-5276
[5]  
Bergman PJ, 2003, CLIN CANCER RES, V9, P1284
[6]   An orthogonal proteomic-genomic screen identifies AIM2 as a cytoplasmic DNA sensor for the inflammasome [J].
Buerckstuemmer, Tilmann ;
Baumann, Christoph ;
Blueml, Stephan ;
Dixit, Evelyn ;
Duernberger, Gerhard ;
Jahn, Hannah ;
Planyavsky, Melanie ;
Bilban, Martin ;
Colinge, Jacques ;
Bennett, Keiryn L. ;
Superti-Furga, Giulio .
NATURE IMMUNOLOGY, 2009, 10 (03) :266-272
[7]   Phase I clinical evaluation of a six-plasmid multiclade HIV-1 DNA candidate vaccine [J].
Catanzaro, Andrew T. ;
Roederer, Mario ;
Koup, Richard A. ;
Bailer, Robert T. ;
Enama, Mary E. ;
Nason, Martha C. ;
Martin, Julie E. ;
Rucker, Steve ;
Andrews, Charla A. ;
Gomez, Phillip L. ;
Mascola, John R. ;
Nabel, Gary J. ;
Graham, Barney S. .
VACCINE, 2007, 25 (20) :4085-4092
[8]   Rip1 mediates the Trif-dependent Toll-like receptor 3- and 4-induced NF-κB activation but does not contribute to interferon regulatory factor 3 activation [J].
Cusson-Hermance, N ;
Khurana, S ;
Lee, TH ;
Fitzgerald, KA ;
Kelliher, MA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (44) :36560-36566
[9]   Activation of c-Jun N-terminal kinase (JNK) pathway by HSV-1 immediate early protein ICP0 [J].
Diao, LR ;
Zhang, BH ;
Xuan, CH ;
Sun, SG ;
Yang, K ;
Tang, YJ ;
Qiao, WT ;
Chen, QM ;
Geng, YQ ;
Wang, C .
EXPERIMENTAL CELL RESEARCH, 2005, 308 (01) :196-210
[10]   Induction of cytotoxic T lymphocytes by intramuscular immunization with plasmid DNA is facilitated by bone marrow-derived cells [J].
Doe, B ;
Selby, M ;
Barnett, S ;
Baenziger, J ;
Walker, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (16) :8578-8583