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High Pulmonary Levels of IL-6 and IL-1beta; in Children with Chronic Suppurative Lung Disease Are Associated with Low Systemic IFN-gamma; Production in Response to Non-Typeable Haemophilus influenzae

机译:慢性化脓性肺疾病患儿肺中高水平的IL-6和IL-1β与对非典型流感嗜血杆菌的低全身性IFN-γ产生有关

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摘要

Non-typeable Haemophilus influenzae (NTHi) is commonly associated with chronic suppurative lung disease in children. We have previously shown that children with chronic suppurative lung disease have a reduced capacity to produce IFN-γ in response to NTHi compared with healthy control children. The aim of this study was to determine if deficient NTHi-specific IFN-γ production is associated with heightened systemic or airway inflammation. We measured a panel of cytokines (IFN-γ, IL-1β, IL-6, IL-8, IL-12 p70), antimicrobial proteins (LL-37, IP-10) as well as cellular and clinical factors associated with airway and systemic inflammation in 70 children with chronic suppurative lung disease. IFN-γ was measured in peripheral blood mononuclear cells challenged in vitro with live NTHi. Regression analysis was used to assess the association between the systemic and airway inflammation and the capacity to produce IFN-γ. On multivariate regression, NTHi-specific IFN-γ production was significantly negatively associated with the BAL concentrations of the inflammatory cytokines IL-6 (β=-0.316; 95%CI -0.49, -0.14; p=0.001) and IL-1β (β=-0.023; 95%CI -0.04, -0.01; p=0.001). This association was independent of bacterial or viral infection, BAL cellularity and the severity of bronchiectasis (using modified Bhalla score on chest CT scans). We found limited evidence of systemic inflammation in children with chronic suppurative lung disease. In summary, increased local airway inflammation is associated with a poorer systemic cell-mediated immune response to NTHi in children with chronic suppurative lung disease. These data support the emerging body of evidence that impaired cell-mediated immune responses and dysregulated airway inflammation may be linked and contribute to the pathobiology of chronic suppurative lung disease.
机译:不可归类的流感嗜血杆菌(NTHi)通常与儿童的慢性化脓性肺疾病有关。先前我们已经表明,与健康对照儿童相比,患有慢性化脓性肺疾病的儿童对NTHi的产生IFN-γ的能力降低。这项研究的目的是确定NTHi特异性IFN-γ产生不足是否与全身或气道炎症加剧有关。我们测量了一组细胞因子(IFN-γ,IL-1β,IL-6,IL-8,IL-12 p70),抗菌蛋白(LL-37,IP-10)以及与气道相关的细胞和临床因素和70例慢性化脓性肺疾病儿童的全身炎症。在体外用活NTHi攻击的外周血单核细胞中测量了IFN-γ。回归分析用于评估全身性和气道炎症与产生IFN-γ的能力之间的关系。多变量回归分析显示,NTHi特异性IFN-γ的产生与炎性细胞因子IL-6(β= -0.316; 95%CI -0.49,-0.14; p = 0.001)和IL-1β(BAL)的浓度显着负相关。 β= -0.023; 95%CI -0.04,-0.01; p = 0.001)。这种关联与细菌或病毒感染,BAL细胞性和支气管扩张的严重性无关(在胸部CT扫描中使用改良的Bhalla评分)。我们发现,患有慢性化脓性肺疾病的儿童出现全身炎症的证据有限。总之,慢性化脓性肺病患儿局部气道炎症增加与对NTHi的全身细胞介导的免疫反应较差有关。这些数据支持了新出现的证据,即细胞介导的免疫应答受损和气道炎症失调可能与慢性化脓性肺病的病理生物学有关,并有助于其发展。

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