van Schaik S M, Tristram D A, Nagpal I S, Hintz K M, Welliver R C, Welliver R C
Department of Pediatrics, State University of New York at Buffalo, School of Medicine and Biomedical Sciences, Buffalo, NY, USA.
J Allergy Clin Immunol. 1999 Apr;103(4):630-6. doi: 10.1016/s0091-6749(99)70235-6.
An imbalance of production of T-helper lymphocyte cytokines, favoring overproduction of IL-4, is believed to be important in the pathogenesis of allergic asthma. However, less is known about the cytokine response in virus-induced wheezing, which is a major cause of morbidity in asthma.
We undertook this study to determine the magnitude of IFN-gamma, IL-4 and IL-10, and leukotriene (LT) responses in infants and children with virus-induced wheezing.
We measured the concentrations of IFN-gamma, IL-4 and IL-10, and cysteinyl LTs in respiratory secretions of 82 infants and young children during acute episodes of virus-induced wheezing. Control subjects were 47 infants and children with uncomplicated upper respiratory infections and 18 normal healthy infants.
Ratios of IFN-gamma to IL-4 were higher (due to increased quantities of IFN-gamma) in subjects with wheezing than in those with upper respiratory infection alone (P =. 003). Quantities of LTs were also increased in wheezing subjects in comparison with those with upper respiratory infections (P =.009). There was a significant correlation between measured concentrations of IFN-gamma and LTs (correlation coefficient =.451, P =.007). Quantities of IL-4 were slightly suppressed in the wheezing groups.
An imbalance favoring overproduction of IFN-gamma appears to be associated temporarily with virus-induced wheezing. A possible mechanism is the enhanced release of LTs from eosinophils or mast cells after sensitization by IFN-gamma.
辅助性T淋巴细胞细胞因子产生失衡,有利于白细胞介素-4的过量产生,这被认为在过敏性哮喘的发病机制中很重要。然而,关于病毒诱导的喘息(这是哮喘发病的主要原因)中的细胞因子反应,人们了解较少。
我们进行这项研究以确定病毒诱导喘息的婴幼儿中干扰素-γ、白细胞介素-4和白细胞介素-10以及白三烯(LT)的反应程度。
我们测量了82例婴幼儿在病毒诱导喘息急性发作期间呼吸道分泌物中干扰素-γ、白细胞介素-4和白细胞介素-10以及半胱氨酰白三烯的浓度。对照组为47例患有单纯上呼吸道感染的婴幼儿和18例正常健康婴幼儿。
喘息患者中干扰素-γ与白细胞介素-4的比值更高(由于干扰素-γ量增加),高于仅患有上呼吸道感染的患者(P = 0.003)。与上呼吸道感染患者相比,喘息患者中的白三烯量也增加(P = 0.009)。测量的干扰素-γ浓度与白三烯之间存在显著相关性(相关系数 = 0.451,P = 0.007)。喘息组中白细胞介素-4的量略有抑制。
有利于干扰素-γ过量产生的失衡似乎与病毒诱导的喘息暂时相关。一种可能的机制是干扰素-γ致敏后嗜酸性粒细胞或肥大细胞释放白三烯增加。