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儿童复发性支气管肺炎伴极高 IgE 水平与白细胞介素 12 受体缺陷。

Interleukin 12 receptor deficiency in a child with recurrent bronchopneumonia and very high IgE levels.

机构信息

Department of Pediatrics, Federico II University, Naples, Italy.

出版信息

Ital J Pediatr. 2012 Sep 19;38:46. doi: 10.1186/1824-7288-38-46.

DOI:10.1186/1824-7288-38-46
PMID:22992471
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3485094/
Abstract

Interleukin-12 (IL-12) is involved in cellular immune responses against intracellular pathogens by promoting the generation of T naive in T helper 1 (Th1) cells and by increasing interferon-gamma (IFN-gamma) production from T and natural killer (NK) cells. A defective induction of a Th1 response may lead to a higher risk of infections, and, in particular, infections due to typical and atypical Mycobacteria. We report on the case of a girl with suffering from recurrent bronchopneumonia associated with very high serum IgE levels, who exhibited a profound impairment of the Th1 generation associated with a novel mutation in the exon 5 of the IL-12R β1 gene (R156H). Our data suggest that in children with severe and recurrent infections, even in the absence of a mycobacterial infection, functional and/or genetic alterations of the molecular mechanisms governing Th1/Th2 homeostasis might be responsible for an atypical immunodeficiency and, therefore, should be investigated in these patients.

摘要

白细胞介素-12(IL-12)通过促进 T 辅助 1(Th1)细胞中 T 幼稚细胞的生成,并增加 T 细胞和自然杀伤(NK)细胞产生干扰素-γ(IFN-γ),参与细胞免疫反应以对抗细胞内病原体。Th1 反应的诱导缺陷可能导致更高的感染风险,特别是由于典型和非典型分枝杆菌引起的感染。我们报告了一例患有反复支气管肺炎并伴有非常高的血清 IgE 水平的女孩,其表现为与 IL-12R β1 基因(R156H)外显子 5中的新型突变相关的 Th1 生成的严重损害。我们的数据表明,在患有严重和反复感染的儿童中,即使没有分枝杆菌感染,也可能是调节 Th1/Th2 平衡的分子机制的功能和/或遗传改变导致了非典型免疫缺陷,因此应在这些患者中进行调查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/579a/3485094/b4de5a83fb83/1824-7288-38-46-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/579a/3485094/d60574f3b5f6/1824-7288-38-46-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/579a/3485094/b4de5a83fb83/1824-7288-38-46-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/579a/3485094/d60574f3b5f6/1824-7288-38-46-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/579a/3485094/b4de5a83fb83/1824-7288-38-46-2.jpg

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