Yabuhara A, Macaubas C, Prescott S L, Venaille T J, Holt B J, Habre W, Sly P D, Holt P G
TVW Telethon Institute for Child Health Research, West Perth, Western Australia.
Clin Exp Allergy. 1997 Nov;27(11):1261-9.
There is increasing evidence that the T-cell reactivity to environmental allergens underlying expression of allergic disease in adulthood, develops initially during childhood. However, there is little information available on the kinetics of these early responses, or on the patterns of cytokine production during this period.
The purpose of this study was twofold: to obtain further information on the reported differences between responses to food versus inhalant allergens during early childhood, and to ascertain the age-range over which T-cell responses to inhalant allergens become polarized towards the TH2 cytokine profile, in potentially atopic children.
In vitro cytokine responses to house dust mite (HDM) and egg (OVA) were assessed by semiquantitative RT-PCR in panels of 2- and 5-year-old children and adults; lymphoproliferative responses to OVA were subjected to epitope analysis.
At age 2 years IL-4/IL-5 responses to HDM grouped with positive atopic family history, and by age 5 years cytokine responses correlated strongly with individual SPT reactivity to HDM. In contrast, OVA responses were restricted to weak and transient IL-5 signals in the 2-year-old family history positive group. Lymphoproliferation assays performed in parallel indicate a log-scale greater postnatal expansion of T-cell reactivity to the inhalant allergen; preliminary epitope analysis of OVA responses indicate that the number of OVA epitopes recognised decrease during early childhood.
Inhalant allergen-specific in vitro cytokine production associated with positive skin-prick test (SPT) reactions, one of the hallmarks of adult atopy, manifests in children at or before 5 years of age; additionally, cytokine responses in SPT negative 5 year-olds are restricted to IFNgamma, as per normal adults. In contrast, T-cell responses to a typical food allergen appear to be deleted during early childhood.
越来越多的证据表明,成年期过敏性疾病表达背后的T细胞对环境过敏原的反应性最初在儿童期就已形成。然而,关于这些早期反应的动力学或此期间细胞因子产生模式的信息却很少。
本研究的目的有两个:一是获取更多关于幼儿期对食物过敏原与吸入性过敏原反应差异的信息;二是确定在潜在特应性儿童中,T细胞对吸入性过敏原的反应向TH2细胞因子谱极化的年龄范围。
通过半定量逆转录聚合酶链反应(RT-PCR)评估2岁、5岁儿童和成人群体对屋尘螨(HDM)和鸡蛋(OVA)的体外细胞因子反应;对OVA的淋巴细胞增殖反应进行表位分析。
2岁时,对HDM的IL-4/IL-5反应与特应性家族史阳性相关,到5岁时,细胞因子反应与个体对HDM的皮肤点刺试验(SPT)反应性密切相关。相比之下,在有家族史阳性的2岁组中,OVA反应仅限于微弱且短暂的IL-5信号。同时进行的淋巴细胞增殖试验表明,T细胞对吸入性过敏原的反应性在出生后呈对数级更大程度的扩展;对OVA反应的初步表位分析表明,幼儿期识别的OVA表位数量减少。
与成人特应性的标志之一——阳性皮肤点刺试验(SPT)反应相关的吸入性过敏原特异性体外细胞因子产生,在5岁及5岁以前的儿童中就已出现;此外,5岁SPT阴性儿童的细胞因子反应如正常成人一样仅限于γ干扰素。相比之下,T细胞对典型食物过敏原的反应在幼儿期似乎被消除。