Bont L, Heijnen C J, Kavelaars A, van Aalderen W M, Brus F, Draaisma J T, Geelen S M, Kimpen J L
University Hospital for Children and Youth "Het Wilhelmina Kinderziekenhuis," Utrecht, The Netherlands.
Am J Respir Crit Care Med. 2000 May;161(5):1518-23. doi: 10.1164/ajrccm.161.5.9904078.
Respiratory syncytial virus (RSV) bronchiolitis is associated with subsequent recurrent wheezing episodes. To determine whether cytokine responses during infection can be of predictive value for the development of recurrent wheezing, we performed a follow-up study in 50 hospitalized children with RSV bronchiolitis. Monocyte and lymphocyte cytokine responses in vitro were studied during the acute phase of disease, and again during the convalescent phase, 3 to 4 wk later. Monocyte cytokine responses, including interleukin-10 (IL-10), were measured in whole blood cultures, stimulated with lipopolysaccharide and interferon-gamma (LPS + IFN-gamma). In addition, T-cell cytokine responses, including IFN-gamma and IL-4 production, were measured in whole-blood cultures stimulated with phytohemagglutinin (PHA) or alphaCD2 + alphaCD28. Cytokine responses were analyzed in relation to the development of recurrent episodes of wheezing, documented by parents in a diary during a 1-yr follow-up period. IL-10 responses during the acute phase of RSV bronchiolitis were comparable to those in healthy control subjects. During the convalescent phase, IL-10 responses were significantly increased in patients as compared with those in healthy control subjects (p < 0.001). At follow-up, 27 children (58%) had recurrent episodes of wheezing. IL-10 levels, measured during the convalescent phase, were significantly higher in patients who developed recurrent wheezing during the year after RSV bronchiolitis than in patients without recurrent episodes of wheezing (p = 0.006). Moreover, IL-10 responses during the convalescent phase correlated significantly with the number of wheezing episodes (r = 0.42, n = 46, p = 0.004). Interestingly, no association was found between IFN-gamma responses, IL-4 responses, or IFNgamma/IL-4 ratios and recurrent wheezing. We conclude that monocyte IL-10 responses in vitro upon stimulation with nonspecific stimuli may have predictive value for the development of recurrent wheezing after RSV bronchiolitis. Moreover, our results indicate that not only allergen-driven Th2 cytokine responses can lead to asthmatic symptoms but also virus-induced changes in cytokine responses may result in asthmatic symptoms.
呼吸道合胞病毒(RSV)细支气管炎与随后的反复喘息发作相关。为了确定感染期间的细胞因子反应是否对反复喘息的发生具有预测价值,我们对50名住院的RSV细支气管炎患儿进行了一项随访研究。在疾病急性期以及3至4周后的恢复期,研究了体外单核细胞和淋巴细胞的细胞因子反应。在全血培养物中,用脂多糖和干扰素-γ(LPS + IFN-γ)刺激后,测量单核细胞细胞因子反应,包括白细胞介素-10(IL-10)。此外,在用植物血凝素(PHA)或αCD2 +αCD28刺激的全血培养物中,测量T细胞细胞因子反应,包括IFN-γ和IL-4的产生。根据家长在1年随访期间日记中记录的反复喘息发作情况,分析细胞因子反应。RSV细支气管炎急性期的IL-10反应与健康对照受试者相当。在恢复期,与健康对照受试者相比,患者的IL-10反应显著增加(p < 0.001)。随访时,27名儿童(58%)有反复喘息发作。在RSV细支气管炎后一年内出现反复喘息的患者中,恢复期测量的IL-10水平显著高于无反复喘息发作的患者(p = 0.006)。此外,恢复期的IL-10反应与喘息发作次数显著相关(r = 0.42,n = 46,p = 0.004)。有趣的是,未发现IFN-γ反应、IL-4反应或IFN-γ/IL-4比值与反复喘息之间存在关联。我们得出结论,体外非特异性刺激后单核细胞IL-10反应可能对RSV细支气管炎后反复喘息的发生具有预测价值。此外,我们的结果表明,不仅变应原驱动的Th2细胞因子反应可导致哮喘症状,病毒诱导的细胞因子反应变化也可能导致哮喘症状。