Department of Biomedical and Molecular Sciences, Queen's University, Kingston, Canada.
Department of Biomedical and Molecular Sciences, Queen's University, Kingston, Canada.
Cytokine. 2018 Aug;108:105-114. doi: 10.1016/j.cyto.2018.03.017. Epub 2018 Mar 27.
Dendritic cells produce IL-12 and IL-23 in response to viral and bacterial infection and these cytokines are responsible for successful pathogen clearance. How sequential viral and bacterial infections affect the production of IL-12 and IL-23 is currently not known. Our study demonstrates that in dendritic cells infected with Lymphocytic choriomeningitis virus (LCMV), TLR activation with bacterial PAMPs resulted in reduced IL-12 and IL-23 expression compared to non-infected cells. Furthermore, expression of other proinflammatory cytokines, TNF-α and IL-6, were not inhibited under these conditions. We discovered that TLR-induced phosphorylation of p38 was significantly inhibited in LCMV-infected cells. We detected enhanced expression of suppressor of cytokine signalling (SOCS)-3 and IL-10. Yet, neutralizing IL-10 did not restore IL-12/IL-23 expression. Taken together, these results show that virus infection interferes with the magnitude of TLR-mediated inflammatory responses by repressing specific cytokine expression.
树突状细胞在受到病毒和细菌感染时会产生 IL-12 和 IL-23,这些细胞因子对于成功清除病原体至关重要。目前尚不清楚连续的病毒和细菌感染如何影响 IL-12 和 IL-23 的产生。我们的研究表明,在感染淋巴细胞性脉络丛脑膜炎病毒 (LCMV) 的树突状细胞中,与非感染细胞相比,细菌 PAMP 的 TLR 激活导致 IL-12 和 IL-23 的表达减少。此外,在这些条件下,其他促炎细胞因子 TNF-α和 IL-6 的表达并未受到抑制。我们发现,LCMV 感染细胞中 TLR 诱导的 p38 磷酸化明显受到抑制。我们检测到细胞因子信号转导抑制剂 (SOCS)-3 和 IL-10 的表达增强。然而,中和 IL-10 并不能恢复 IL-12/IL-23 的表达。综上所述,这些结果表明病毒感染通过抑制特定细胞因子的表达来干扰 TLR 介导的炎症反应的幅度。