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常见可变免疫缺陷病患者血清白细胞介素(IL)-12p40水平升高及外周血树突状细胞减少:IL-12p40和干扰素-γ基因分析

Elevated serum interleukin (IL)-12p40 levels in common variable immunodeficiency disease and decreased peripheral blood dendritic cells: analysis of IL-12p40 and interferon-gamma gene.

作者信息

Martinez-Pomar N, Raga S, Ferrer J, Pons J, Munoz-Saa I, Julia M-R, de Gracia J, Matamoros N

机构信息

Immunology Service, Hospital Universitari Son Dureta, Palma de Mallorca, Andrea Doria 55, Balearic Island 07014, Spain.

出版信息

Clin Exp Immunol. 2006 May;144(2):233-8. doi: 10.1111/j.1365-2249.2006.03063.x.

DOI:10.1111/j.1365-2249.2006.03063.x
PMID:16634796
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1809649/
Abstract

Common variable immunodeficiency disease (CVID) is a heterogeneous syndrome characterized by low immunoglobulin serum levels and recurrent bacterial infections. Several studies suggest that CVID patients have a polarized immune response towards a T helper type 1 phenotype (TH1). However, the factors causing the TH1 polarization remain to be determined in this disease. In the present study, serum interleukin (IL)-12, interferon (IFN)-gamma levels and the IL-12p40 and IFN-gamma gene were studied in CVID patients. Furthermore, we evaluate dendritic cells (DCs) compartment, myeloid dendritic cells (mDCs) and plasmocytoid dendritic cells (pDCs), which help to differentiate naive T cells preferentially into TH1 and TH2, respectively. The serum IL-12p40 subunit levels were increased significantly in CVID patients compared to healthy controls. We examined whether these elevated serum IL-12p40 levels are associated with IFN-gamma or IL-12p40 gene polymorphisms, or with new mutations in the IL-12p40 promoter gene. In our hands, no new mutations were found and gene polymorphisms frequencies in CVID patients were similar to the control population. In conclusion, the elevated serum levels of IL-12p40 found in our CVID patients were not related to these genetic variations. The DC compartment analysis did not show an imbalance between pDCs and mDCs, but revealed the presence of low numbers and percentage of both DC populations in CVID.

摘要

普通可变免疫缺陷病(CVID)是一种异质性综合征,其特征为血清免疫球蛋白水平低下和反复发生细菌感染。多项研究表明,CVID患者对1型辅助性T细胞(TH1)表型具有极化免疫反应。然而,导致TH1极化的因素在该疾病中仍有待确定。在本研究中,对CVID患者的血清白细胞介素(IL)-12、干扰素(IFN)-γ水平以及IL-12p40和IFN-γ基因进行了研究。此外,我们评估了树突状细胞(DC)亚群,即髓样树突状细胞(mDC)和浆细胞样树突状细胞(pDC),它们分别有助于将初始T细胞优先分化为TH1和TH2。与健康对照相比,CVID患者的血清IL-12p40亚基水平显著升高。我们检查了这些升高的血清IL-12p40水平是否与IFN-γ或IL-12p40基因多态性相关,或者与IL-12p40启动子基因的新突变相关。在我们的研究中,未发现新的突变,CVID患者的基因多态性频率与对照人群相似。总之,我们在CVID患者中发现的血清IL-12p40水平升高与这些基因变异无关。DC亚群分析未显示pDC和mDC之间存在失衡,但揭示了CVID中两种DC群体的数量和百分比均较低。

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