Sá-Nunes Anderson, Bafica André, Lucas David A, Conrads Thomas P, Veenstra Timothy D, Andersen John F, Mather Thomas N, Ribeiro José M C, Francischetti Ivo M B
Section of Vector Biology, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases/National Institutes of Health, Rockville, MD 20852, USA.
J Immunol. 2007 Aug 1;179(3):1497-505. doi: 10.4049/jimmunol.179.3.1497.
Tick saliva is thought to contain a number of molecules that prevent host immune and inflammatory responses. In this study, the effects of Ixodes scapularis saliva on cytokine production by bone marrow-derived dendritic cells (DCs) from C57BL/6 mice stimulated by TLR-2, TLR-4, and TLR-9 ligands were studied. Saliva at remarkably diluted concentrations (<1/2000) promotes a dose-dependent inhibition of IL-12 and TNF-alpha production induced by all TLR ligands used. Using a combination of fractionation techniques (microcon filtration, molecular sieving, and reversed-phase chromatography), we unambiguously identified PGE(2) as the salivary inhibitor of IL-12 and TNF-alpha production by DCs. Moreover, we have found that I. scapularis saliva (dilution 1/200; approximately 10 nM PGE(2)) marginally inhibited LPS-induced CD40, but not CD80, CD86, or MHC class II expression. In addition, saliva significantly suppressed the ability of DCs to stimulate Ag-specific CD4(+) T cell proliferation and IL-2 production. Notably, the effect of saliva on DC maturation and function was reproduced by comparable concentrations of standard PGE(2). These findings indicate that PGE(2) accounts for most inhibition of DC function observed with saliva in vitro. The role of salivary PGE(2) in vector-host interaction and host immune modulation and inflammation in vivo is also discussed. This study is the first to identify molecularly a DC inhibitor from blood-sucking arthropods.
蜱虫唾液被认为含有多种可阻止宿主免疫和炎症反应的分子。在本研究中,研究了肩突硬蜱唾液对C57BL/6小鼠骨髓来源的树突状细胞(DCs)在受到TLR-2、TLR-4和TLR-9配体刺激时细胞因子产生的影响。显著稀释浓度(<1/2000)的唾液可促进对所有所用TLR配体诱导的IL-12和TNF-α产生的剂量依赖性抑制。通过结合分级分离技术(微滤、分子筛和反相色谱),我们明确鉴定出PGE(2)是DCs产生IL-12和TNF-α的唾液抑制剂。此外,我们发现肩突硬蜱唾液(稀释1/200;约10 nM PGE(2))对LPS诱导的CD40有轻微抑制作用,但对CD80、CD86或MHC II类分子的表达无抑制作用。此外,唾液显著抑制了DCs刺激抗原特异性CD4(+) T细胞增殖和IL-2产生的能力。值得注意的是,唾液对DC成熟和功能的影响可被相当浓度的标准PGE(2)重现。这些发现表明,PGE(2)是体外观察到的唾液对DC功能的大部分抑制作用的原因。还讨论了唾液中PGE(2)在载体-宿主相互作用以及体内宿主免疫调节和炎症中的作用。本研究首次从吸血节肢动物中分子鉴定出一种DC抑制剂。