Differential effects of CpG-DNA in Toll-like receptor-2/-4/-9 tolerance and cross-tolerance

被引:94
作者
Dalpke, AH [1 ]
Lehner, MD
Hartung, T
Heeg, K
机构
[1] Heidelberg Univ, Dept Hyg & Med Microbiol, INF 324, D-69120 Heidelberg, Germany
[2] Univ Marburg, Inst Med Microbiol & Hyg, Marburg, Germany
[3] Univ Konstanz, D-7750 Constance, Germany
关键词
CpG-DNA; lipopolysaccharide; lipoteichoic acid; tolerance; Toll-like receptors;
D O I
10.1111/j.1365-2567.2005.02211.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lipopolysaccharide (LPS) tolerance is a state of refractoriness towards a second stimulation by LPS after a preceding stimulation. LPS is recognized by Toll-like receptor-4 (TLR-4), which belongs to a group of pattern recognition receptors mediating activation of innate immunity by microbial components. To date, it is not known in detail to what extent other TLR-dependent stimuli also induce tolerance and whether preceding and challenging stimuli are interchangeable. We have examined tolerance induction in detail for lipoteichoic acid (LTA), LPS and CpG-DNA, which are recognized by TLR-2, -4 and -9, respectively. In RAW264.7 macrophages, all three stimuli induced tolerance towards a subsequent challenge with the same stimulus used for priming, as well as cross-tolerance towards subsequent challenge with other stimuli signalling via different TLRs. However, whereas LPS/LTA cross-tolerance was also functional in an in vivo model of galactosamine (GalN)-primed liver damage, pretreatment with CpG only protected against GalN/CpG challenge and failed to induce cross-tolerance for LPS and LTA. CpG-DNA pretreatment even enhanced tumour necrosis factor (TNF)-alpha production and liver damage upon subsequent challenge with LPS or LTA. Stimulation with CpG-DNA resulted in a peculiar sensitization for interferon (IFN)-gamma secretion. The data indicate that, in contrast to in vitro macrophage desensitization, the in vivo consequences of repeated TLR stimulation greatly differ amongst different TLR ligands.
引用
收藏
页码:203 / 212
页数:10
相关论文
共 50 条
  • [1] Toll-like receptor signalling
    Akira, S
    Takeda, K
    [J]. NATURE REVIEWS IMMUNOLOGY, 2004, 4 (07) : 499 - 511
  • [2] Toll-like receptors differentially induce nucleosome remodelling at the IL-12p40 promoter
    Albrecht, I
    Tapmeier, T
    Zimmermann, S
    Frey, M
    Heeg, K
    Dalpke, A
    [J]. EMBO REPORTS, 2004, 5 (02) : 172 - 177
  • [3] Clinical review: Immunodepression in the surgical patient and increased susceptibility to infection
    Angele M.K.
    Faist E.
    [J]. Critical Care, 6 (4): : 298 - 305
  • [4] 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
  • [5] Bundschuh DS, 1997, J IMMUNOL, V158, P2862
  • [6] Cowdery J, 1996, J IMMUNOL, V156, P4570
  • [7] Cowdery JS, 1999, J IMMUNOL, V162, P6770
  • [8] Preexposure of murine macrophages to CpG oligonucleotide results in a biphasic tumor necrosis factor alpha response to subsequent lipopolysaccharide challenge
    Crabtree, TD
    Jin, L
    Raymond, DP
    Pelletier, SJ
    Houlgrave, CW
    Gleason, TG
    Pruett, TL
    Sawyer, RG
    [J]. INFECTION AND IMMUNITY, 2001, 69 (04) : 2123 - 2129
  • [9] Induction of in vitro reprogramming by toll-like receptor (TLR)2 and TLR4 agonists in murine macrophages:: Effects of TLR "homotolerance" versus "heterotolerance" on NF-κB signaling pathway components
    Dobrovolskaia, MA
    Medvedev, AE
    Thomas, KE
    Cuesta, N
    Toshchakov, V
    Ren, TB
    Cody, MJ
    Michalek, SM
    Rice, NR
    Vogel, SN
    [J]. JOURNAL OF IMMUNOLOGY, 2003, 170 (01) : 508 - 519
  • [10] Mal (MyD88-adapter-like) is required for Toll-like receptor-4 signal transduction
    Fitzgerald, KA
    Palsson-McDermott, EM
    Bowie, AG
    Jefferies, CA
    Mansell, AS
    Brady, G
    Brint, E
    Dunne, A
    Gray, P
    Harte, MT
    McMurray, D
    Smith, DE
    Sims, JE
    Bird, TA
    O'Neill, LAJ
    [J]. NATURE, 2001, 413 (6851) : 78 - 83