PathWest Laboratory Medicine WA, Perth 6009, Australia.
Faculty of Health and Medical Sciences, University of Western Australia, Perth 6009, Australia.
Viruses. 2019 Nov 7;11(11):1038. doi: 10.3390/v11111038.
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.
鼻病毒 C 是导致哮喘和非哮喘儿童因间歇性喘息而住院的重要病原体。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相关,但尚未在 RV-C 感染儿童中进行研究。我们确定了这些儿童的鼻细胞因子谱,并研究了它们与 RV-C 载量和临床结果的关系。从因急性喘息和急性上呼吸道病毒感染而到玛格丽特公主医院急诊科就诊的 24-72 个月大的儿童中采集装有纤维的鼻拭子。通过定量 RT-PCR 确定 RV-C 载量,并用商业的人类细胞因子 34 plex 面板来描述细胞因子谱。RV-C 是学龄前儿童因间歇性喘息而住院的最常见病毒。哮喘和非哮喘患者的 RV-C 载量无显著差异。两组均显示出基于 Th2 的细胞因子谱。然而,在患有预先存在哮喘的 RV-C 感染儿童中,仅升高了 Th17 反应细胞因子 IL-17 和 IL-1β。在这项研究中,无论是 RV-C 载量还是任何特定细胞因子都与疾病严重程度无关。需要医疗干预的 RV-C 引起的喘息以 Th2 炎症模式为特征,与病毒载量无关。任何治疗干预措施都应针对感染后宿主反应进行调节。