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Sex Differences in the Response to Viral Infections: TLR8 and TLR9 Ligand Stimulation Induce Higher IL10 Production in Males

机译:对病毒感染的反应中的性别差异:TLR8和TLR9配体刺激导致男性产生更高的IL10。

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摘要

Background: Susceptibility to viral infections as well as their severity are higher in men than in women. Heightened antiviral responses typical of women are effective for rapid virus clearance, but if excessively high or prolonged, can result in chronic/inflammatory pathologies. We investigated whether this variability could be in part attributable to differences in the response to the Toll-Like Receptors (TLR) more involved in the virus recognition. Methods: Cytokine production by peripheral blood mononuclear cells (PBMCs) from male and female healthy donors after stimulation with Toll-like receptors (TLR) 3, 7, 8, 9 ligands or with viruses (influenza and Herpes-simplex-1) was evaluated. Results: Compared to females, PBMCs from males produced not only lower amounts of IFN-alpha in response to TLR7 ligands but also higher amounts of the immunosuppressive cytokine IL10 after stimulation with TLR8 and TLR9 ligands or viruses. IL10 production after TLR9 ligands or HSV-1 stimulation was significantly related with plasma levels of sex hormones in both groups, whereas no correlation was found in cytokines produced following TLR7 and TLR8 stimulation. Conclusions: Given the role of an early production of IL10 by cells of innate immunity in modulating innate and adaptive immune response to viruses, we suggest that sex-related difference in its production following viral nucleic acid stimulation of TLRs may be involved in the sex-related variability in response to viral infections.
机译:背景:男性对病毒感染的易感性及其严重程度高于女性。女性典型的增强抗病毒反应可快速清除病毒,但如果过高或过长,则会导致慢性/炎症性病变。我们调查了这种可变性是否部分归因于对病毒识别中更多涉及的Toll样受体(TLR)的反应差异。方法:评估了用Toll样受体(TLR)3、7、8、9配体或病毒(流感和疱疹-单纯疱疹1型)刺激后,男性和女性健康供体的外周血单个核细胞(PBMC)产生的细胞因子。 。结果:与雌性相比,雄性的PBMC在响应TLR7和TLR9配体或病毒刺激后,不仅产生较少量的IFN-α响应TLR7配体,而且产生较高量的免疫抑制细胞因子IL10。在两组中,TLR9配体或HSV-1刺激后IL10的产生与血浆性激素水平显着相关,而在TLR7和TLR8刺激后产生的细胞因子中没有相关性。结论:鉴于先天性免疫细胞早期产生IL10在调节对病毒的先天性和适应性免疫应答中的作用,我们建议在通过病毒核酸刺激TLRs后产生性相关的差异可能与性相关。病毒感染的相关变异性。

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