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Nasal Cytokine Profiles of Patients Hospitalised with Respiratory Wheeze Associated with Rhinovirus C

机译:鼻呼吸病合并鼻病毒C住院患者的鼻细胞因子谱

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摘要

Background: Rhinovirus C is an important pathogen of asthmatic and non-asthmatic children hospitalised with episodic wheeze. Previous studies on other respiratory viruses have shown that several host cytokines correlate with duration of hospitalisation, but this has yet to be investigated in children with RV-C infection. We determined the nasal cytokine profiles of these children and investigated their relationship with RV-C load and clinical outcome. Flocked nasal swabs were collected from children aged 24–72 months presenting to the Emergency Department at Princess Margaret Hospital with a clinical diagnosis of acute wheeze and an acute upper respiratory tract viral infection. RV-C load was determined by quantitative RT-PCR and cytokine profiles were characterised by a commercial human cytokine 34-plex panel. RV-C was the most commonly detected virus in pre-school-aged children hospitalised with an episodic wheeze. RV-C load did not significantly differ between asthmatic and non-asthmatic patients. Both groups showed a Th2-based cytokine profile. However, Th17 response cytokines IL-17 and IL-1β were only elevated in RV-C-infected children with pre-existing asthma. Neither RV-C load nor any specific cytokines were associated illness severity in this study. Medically attended RV-C-induced wheeze is characterised by a Th2 inflammatory pattern, independent of viral load. Any therapeutic interventions should be aimed at modulating the host response following infection.
机译:背景:鼻病毒C是哮喘和非哮喘儿童的发作性喘息的重要病原体。先前对其他呼吸道病毒的研究表明,几种宿主细胞因子与住院时间有关,但是尚未对患有RV-C感染的儿童进行调查。我们确定了这些儿童的鼻细胞因子谱,并调查了它们与RV-C负荷和临床结局的关系。从呈报给玛格丽特公主医院急诊科的24-72个月大的儿童中收集了成群的鼻拭子,临床诊断为急性喘鸣和急性上呼吸道病毒感染。 RV-C负荷是通过定量RT-PCR确定的,而细胞因子谱则是通过商业化的人类细胞因子34-plex面板来表征的。在因发作性喘息而住院的学龄前儿童中,RV-C是最常见的病毒。哮喘和非哮喘患者的RV-C负荷无明显差异。两组均显示基于Th2的细胞因子谱。然而,仅在RV-C感染的哮喘患者中,Th17应答细胞因子IL-17和IL-1β升高。在这项研究中,RV-C负荷和任何特定的细胞因子均与疾病的严重程度无关。医学上由RV-C引起的喘息的特征是Th2炎症模式,与病毒载量无关。任何治疗干预措施均应旨在调节感染后的宿主反应。

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