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
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