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TNFRSF13B(TACI)基因多态性在西班牙免疫球蛋白A缺乏症患者中的作用

Role of polymorphisms in the TNFRSF13B (TACI) gene in Spanish patients with immunoglobulin A deficiency.

作者信息

López-Mejías R, del Pozo N, Fernández-Arquero M, Ferreira A, García-Rodríguez M C, de la Concha E G, Fontán G, Urcelay E, Martínez A, Núñez C

机构信息

Department of Clinical Immunology, Hospital Clínico San Carlos, Madrid, Spain.

出版信息

Tissue Antigens. 2009 Jul;74(1):42-5. doi: 10.1111/j.1399-0039.2009.01253.x. Epub 2009 Apr 6.

Abstract

Mutations in the TNFRSF13B (TACI) gene have been associated with common variable immunodeficiency, and a role in immunoglobulin A deficiency (IgAD) has also been suggested. We aimed at studying the role of several polymorphisms along this gene in IgAD susceptibility. Three TNFRSF13B mutations (C104R, A181E and R202H) and eight additional single nucleotide polymorphisms in the gene were genotyped in 338 Spanish IgAD patients and 553 ethnically matched healthy controls and tested for association. Data from parents of 114 IgAD patients were also collected and used for additional analysis. No statistically significant differences were observed after comparing patients and controls for any single nucleotide polymorphism analysed. Therefore, our work seems to discard a role of TNFRSF13B mutations in IgAD, concordantly with the most recent published studies.

摘要

肿瘤坏死因子受体超家族成员13B(TACI)基因突变与常见变异型免疫缺陷有关,也有人提出其在免疫球蛋白A缺乏症(IgAD)中起作用。我们旨在研究该基因上几个多态性位点在IgAD易感性中的作用。对338名西班牙IgAD患者和553名种族匹配的健康对照者进行了该基因的三个肿瘤坏死因子受体超家族成员13B突变(C104R、A181E和R202H)及另外八个单核苷酸多态性的基因分型,并检测其关联性。还收集了114名IgAD患者父母的数据用于进一步分析。对所分析的任何单核苷酸多态性在患者和对照之间进行比较后,未观察到统计学上的显著差异。因此,与最近发表的研究一致,我们的研究似乎排除了肿瘤坏死因子受体超家族成员13B突变在IgAD中的作用。

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