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[热性惊厥患儿特异性体液免疫反应紊乱]

[Disorders of specific humoral immunological response in children with febrile seizures].

作者信息

Zubiel Maria, Wendorff Janusz, Zeman Krzysztof, Tosik Marcin

机构信息

Klinika Neurologii, Instytut Centrum Zdrowia Matki Polki, ul. Rzgowska 281/289, 93-338 Łódź.

出版信息

Neurol Neurochir Pol. 2004;38(1 Suppl 1):S39-44.

Abstract

The aim of the study was to analyse a few recent aspects concerning the humoral immunological response deficiency in children with febrile seizures. 33 children were involved in the study: 16 with a single fit of febrile seizures and 17 with more than one fit. Children's average age was 37.6 months. The control group consisted of 14 healthy children chosen according to the age criterion. In the last three weeks there were no symptoms of infection. Blood for immunological tests was taken in the interictal period. In each case blood was taken for evaluation of B lymphocytes subpopulation (CD19/CD5, CD19/CD10, CD19/CD21), T lymphocytes (CD4/CD45RA, CD4/CD45RO) and the proliferative response to the action of PWM and PHA mitogens. The concentrations of released IgA, IgG, IgM and subgroups of IgG were also measured. In the children's group with single febrile seizures there were statistically higher levels of lymphocytes: CD19/CD5 and CD19/CD21, lower level of T lymphocytes: CD4/CD45RA and CD4/CD45RO, poorer lymphocyte response to the action of PWM and PHA mitogens. Moreover there were lower concentrations of the total IgG and IgG2 and IgG4 subgroups. In children who had only one fit of febrile seizures, abnormalities in the conducted tests were expressed much more than in the control group and the children's group with the multiple febrile seizures. The results suggest that there is a connection between the genetic factors and the dysfunction of immunological system and the course of febrile seizures.

摘要

本研究的目的是分析近期一些与热性惊厥患儿体液免疫反应缺陷相关的方面。33名儿童参与了该研究:16名仅有一次热性惊厥发作,17名有不止一次发作。儿童的平均年龄为37.6个月。对照组由14名根据年龄标准选取的健康儿童组成。在过去三周内无感染症状。在发作间期采集血液进行免疫检测。在每种情况下,采集血液以评估B淋巴细胞亚群(CD19/CD5、CD19/CD10、CD19/CD21)、T淋巴细胞(CD4/CD45RA、CD4/CD45RO)以及对PWM和PHA有丝分裂原作用的增殖反应。还测量了释放的IgA、IgG、IgM浓度以及IgG亚群。在仅有一次热性惊厥发作的儿童组中,淋巴细胞水平在统计学上较高:CD19/CD5和CD19/CD21,T淋巴细胞水平较低:CD4/CD45RA和CD4/CD45RO,淋巴细胞对PWM和PHA有丝分裂原作用的反应较差。此外,总IgG以及IgG2和IgG4亚群的浓度较低。在仅有一次热性惊厥发作的儿童中,所进行检测中的异常表现比对照组和有多次热性惊厥发作的儿童组更为明显。结果表明,遗传因素与免疫系统功能障碍以及热性惊厥的病程之间存在关联。

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