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Production of Interleukin-20 cytokines limits bacterial clearance and lung inflammation during infection by Streptococcus pneumoniae

机译:白细胞介素20细胞因子的产生限制了肺炎链球菌感染期间的细菌清除率和肺部炎症

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Background Streptococcus pneumoniae is the leading cause of bacterial pneumonia worldwide. Previous reports showed that IL-20 cytokines (IL-19, IL-20 and IL-24) are induced and have an immuno-regulatory function during cutaneous infection. In the current study, our aim was to demonstrate the implication of IL-20 cytokines and their receptors and their role during experimental pneumococcal infection. Methods C57BL/6 mice were infected with S. pneumoniae by intranasal route . The bacterial burden, the immune response and the cytokine production were evaluated after treatment with an anti-IL-20 receptor-b (IL-20Rb) neutralizing antibody (anti-IL-20Rb). Findings Of interest, expression of IL-20 cytokines mRNA and protein were transiently increased in the lung tissue during infection. Blocking of the IL-20Rb decreased the bacterial burden both in the bronchoalveolar lavage and the lung whereas there was no significant drop in the blood. This treatment also reduced the pulmonary damages (as shown by the alveolar wall thickening), the recruitment of neutrophils and dendritic cells, and the levels of the pro-inflammatory cytokines IL-1β and IL-6 in the lung. Administration of the anti-IL-20Rb antibody enhanced the synthesis of the antibacterial peptide LCN2. However, this effect is transient and did not affect the survival of the infected mice. Interpretation Collectively, this study highlights the implication of IL-20 related cytokines during lung infection by S. pneumoniae and might have therapeutic applications in bacterial pneumonia. Fundings This work was supported by CNRS, INSERM, INSERM-transfert, the University of Lille and the Fondation du Souffle (Paris, France).
机译:背景技术肺炎链球菌是全世界细菌性肺炎的主要原因。先前的报道表明,IL-20细胞因子(IL-19,IL-20和IL-24)被诱导并在皮肤感染期间具有免疫调节功能。在当前的研究中,我们的目的是证明IL-20细胞因子及其受体的含义及其在实验性肺炎球菌感染中的作用。方法C57BL / 6小鼠经鼻内途径感染肺炎链球菌。用抗IL-20受体-b(IL-20Rb)中和抗体(抗IL-20Rb)处理后,评估细菌负担,免疫应答和细胞因子产生。有趣的发现,在感染过程中,肺组织中IL-20细胞因子的mRNA和蛋白的表达瞬时增加。 IL-20Rb的阻断减少了支气管肺泡灌洗和肺中的细菌负担,而血液中却没有明显的下降。这种治疗还减少了肺损伤(如肺泡壁增厚所示),中性粒细胞和树突状细胞的募集以及肺中促炎性细胞因子IL-1β和IL-6的水平。抗IL-20Rb抗体的施用增强了抗菌肽LCN2的合成。但是,这种作用是暂时的,不会影响被感染小鼠的存活。总体而言,该研究突出了肺炎链球菌在肺部感染期间与IL-20相关的细胞因子的含义,并且可能在细菌性肺炎中具有治疗应用。资金这项工作得到了CNRS,INSERM,INSERM转让,里尔大学和Souffle基金会(法国巴黎)的支持。

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