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过敏性疾病患儿的血清白细胞介素4和可溶性CD23水平。

Serum levels of interleukin 4 and soluble CD23 in children with allergic disorders.

作者信息

Ohshima Y, Katamura K, Miura M, Mikawa H, Mayumi M

机构信息

Department of Paediatrics, Minami-Kyoto National Hospital, Japan.

出版信息

Eur J Pediatr. 1995 Sep;154(9):723-8. doi: 10.1007/BF02276715.

Abstract

UNLABELLED

In order to clarify the clinical significance of serum interleukin 4 (IL-4) levels, we measured serum IL-4 concentrations in allergic and non-allergic children using a highly sensitive sandwich ELISA. The limit of detection of the assay was 0.15 pg/ml in serum samples. Serum IL-4 was detected in 96.3% (53/55) of non-allergic controls, in 92.9% (183/197) of allergic children, in 70% (7/10) of cord blood samples and in 86.7% (26/30) of neonates. The IL-4 levels in sera from non-allergic controls were relatively constant during the ages examined and all samples were under 1.5 pg/ml. In allergic children, the serum levels of IL-4 were significantly elevated, particularly at age 13-24 months. The serum levels of IL-4 did not differ in children with different clinical manifestations of allergy, such as bronchial asthma, and atopic dermatitis. The serum level of soluble CD23 (sCD23) showed an age-dependent change in allergic and non-allergic children and was significantly higher in allergic than in non-allergic infants aged 7 to 12 months, but not in other age groups. There was no significant correlation among serum levels of IL-4, sCD23 and IgE.

CONCLUSION

It is suggested that the measurement of serum IL-4 and sCD23 is helpful in the examination of allergic patients in infancy and early childhood, but neither the serum level of IL-4 nor sCD23 directly reflects in vivo IgE production.

摘要

未标记

为了阐明血清白细胞介素4(IL-4)水平的临床意义,我们使用高灵敏度夹心酶联免疫吸附测定法(ELISA)测量了过敏性和非过敏性儿童的血清IL-4浓度。该检测方法在血清样本中的检测限为0.15 pg/ml。在96.3%(53/55)的非过敏性对照、92.9%(183/197)的过敏性儿童、70%(7/10)的脐带血样本以及86.7%(26/30)的新生儿中检测到了血清IL-4。在检查的年龄段中,非过敏性对照血清中的IL-4水平相对稳定,所有样本均低于1.5 pg/ml。在过敏性儿童中,血清IL-4水平显著升高,尤其是在13 - 24个月龄时。不同过敏临床表现(如支气管哮喘和特应性皮炎)的儿童血清IL-4水平没有差异。可溶性CD23(sCD23)的血清水平在过敏性和非过敏性儿童中呈现年龄依赖性变化,在7至12个月龄的过敏性婴儿中显著高于非过敏性婴儿,但在其他年龄组中并非如此。血清IL-4、sCD23和IgE水平之间没有显著相关性。

结论

建议测量血清IL-4和sCD23有助于婴幼儿期过敏性患者的检查,但血清IL-4水平和sCD23均不能直接反映体内IgE的产生。

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