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变应原诱导的儿童细胞因子产生、特应性疾病、免疫球蛋白E及喘息

Allergen-induced cytokine production, atopic disease, IgE, and wheeze in children.

作者信息

Contreras J Paola, Ly Ngoc P, Gold Diane R, He Hongzhen, Wand Mathew, Weiss Scott T, Perkins David L, Platts-Mills Thomas A E, Finn Patricia W

机构信息

Pulmonary and Critical Care Division, Brigham and Women's Hospital, Boston, MA 02115, USA.

出版信息

J Allergy Clin Immunol. 2003 Dec;112(6):1072-7. doi: 10.1016/j.jaci.2003.08.036.

Abstract

BACKGROUND

The early childhood allergen-induced immune responses associated with atopic disease and IgE production in early life are not well understood.

OBJECTIVE

We assessed the relationship of allergen-induced cytokine production by PBMCs to both atopic disease and to IgE increase in a cohort of children with a parental history of allergy or asthma (n = 112) at a median of 2 years of age. We examined cockroach (Bla g 1)-induced, house dust mite (Der f 1)-induced, and cat (Fel d 1)-induced cytokine secretion, including secretion of IFN-gamma, IL-13, IL-10, and TNF-alpha. We investigated whether distinct cytokine patterns associated with atopic disease can be detected in immune responses of children.

METHODS

PBMCs were isolated, and allergen-induced cytokine secretion was analyzed by means of ELISA. Atopic disease was defined as physician- or nurse-diagnosed eczema or hay fever. Increased IgE was defined as an IgE level of greater than 35 U/mL to dust mite, cockroach, cat, and egg white or a total IgE level of 60 U/mL or greater.

RESULTS

Compared with children without atopic disease, children with atopic disease had lower Der f 1 (P =.005) and Bla g 2 (P =.03) allergen-induced IFN-gamma levels. Compared with children without increased IgE (n = 95), those with increased IgE (n = 16) had higher Der f 1-induced (P =.006) and Fel d 1-induced (P =.005) IL-13 levels and lower Bla g 2-induced (P =.03) IFN-gamma levels. Compared with children with neither atopic disease nor repeated wheeze, children with both atopic disease and repeated wheeze had lower levels of allergen-induced IFN-gamma (P =.01 for Der f 1 and P =.02 for Bla g 2) cytokine secretion.

CONCLUSION

In young children at risk for asthma or allergy, decreased allergen-induced IFN-gamma secretion is associated with atopic disease and, in some cases, with increased IgE levels. Increased allergen-induced IL-13 secretion is most strongly associated with early life increase of IgE.

摘要

背景

与特应性疾病及生命早期IgE产生相关的幼儿期变应原诱导的免疫反应尚未完全明确。

目的

我们评估了在一组有父母过敏或哮喘病史的儿童(n = 112)中,年龄中位数为2岁时,外周血单核细胞(PBMCs)变应原诱导的细胞因子产生与特应性疾病及IgE升高之间的关系。我们检测了蟑螂(Bla g 1)诱导、屋尘螨(Der f 1)诱导和猫(Fel d 1)诱导的细胞因子分泌,包括γ干扰素(IFN-γ)、白细胞介素13(IL-13)、白细胞介素10(IL-10)和肿瘤坏死因子α(TNF-α)的分泌。我们研究了在儿童免疫反应中是否能检测到与特应性疾病相关的不同细胞因子模式。

方法

分离PBMCs,采用酶联免疫吸附测定(ELISA)分析变应原诱导的细胞因子分泌。特应性疾病定义为由医生或护士诊断的湿疹或花粉症。IgE升高定义为对尘螨、蟑螂、猫和蛋清的IgE水平大于35 U/mL或总IgE水平为60 U/mL或更高。

结果

与无特应性疾病的儿童相比,患有特应性疾病的儿童Der f 1(P = 0.005)和Bla g 2(P = 0.03)变应原诱导的IFN-γ水平较低。与IgE未升高的儿童(n = 95)相比,IgE升高的儿童(n = 16)Der f 1诱导的(P = 0.006)和Fel d 1诱导的(P = 0.005)IL-13水平较高,而Bla g 2诱导的(P = 0.03)IFN-γ水平较低。与既无特应性疾病也无反复喘息的儿童相比,患有特应性疾病且有反复喘息的儿童变应原诱导的IFN-γ细胞因子分泌水平较低(Der f 1为P = 0.01,Bla g 2为P = 0.02)。

结论

在有哮喘或过敏风险的幼儿中,变应原诱导的IFN-γ分泌减少与特应性疾病相关,在某些情况下,与IgE水平升高相关。变应原诱导的IL-13分泌增加与生命早期IgE升高最密切相关。

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