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有特应性疾病家族史的新生儿和婴儿中的IgE与特应性过敏

IgE and atopic allergy in newborns and infants with a family history of atopic disease.

作者信息

Kjellman N I, Johansson S G

出版信息

Acta Paediatr Scand. 1976 Sep;65(5):601-7. doi: 10.1111/j.1651-2227.1976.tb04939.x.

Abstract

Serum IgE levels were studied in 2 groups of children with a family history of atopic disease, 30 in whom the mother only and 38 in whom both parents had atopic disease. IgE antibodies were determined with Phadebas RAST Test and serum IgE with Phadebas IgE Test and Phadebas PRIST at 0, 3, 9, 12 and 18 months of age. There was no correlation between the serum IgE levels in mothers and their newborns. RAST tests were frequently positive in maternal sera but no positive RAST test was found in the newborns. Obvious and probable atopic disease developed during the observation period in 42.1% of the children with a double family history of atopic disease. In 75% of these the serum IgE level was above the upper limit of normal on an average 6 months before the onset of atopic symptoms. An elevated IgE level without atopic symptoms during the observation period occurred in only one child. It is concluded that the serum IgE in newborns seems to be of foetal origin and that the determination of serum IgE in infants is of value in predicting atopic allergy.

摘要

对两组有特应性疾病家族史的儿童进行了血清IgE水平研究,其中一组30名儿童的母亲患有特应性疾病,另一组38名儿童的父母双方都患有特应性疾病。在0、3、9、12和18个月龄时,用Phadebas RAST试验测定IgE抗体,用Phadebas IgE试验和Phadebas PRIST测定血清IgE。母亲及其新生儿的血清IgE水平之间没有相关性。RAST试验在母亲血清中经常呈阳性,但在新生儿中未发现阳性RAST试验结果。在有特应性疾病双重家族史的儿童中,42.1%在观察期内出现明显和可能的特应性疾病。其中75%的儿童在特应性症状出现前平均6个月血清IgE水平高于正常上限。在观察期内,只有一名儿童出现IgE水平升高但无特应性症状的情况。结论是,新生儿的血清IgE似乎来源于胎儿,并且测定婴儿血清IgE对预测特应性过敏有价值。

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