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共济失调毛细血管扩张症患者完全类别转换缺陷的临床意义。

The clinical significance of complete class switching defect in Ataxia telangiectasia patients.

作者信息

Ghiasy Saleh, Parvaneh Leila, Azizi Gholamreza, Sadri Ghazal, Zaki Dizaji Majid, Abolhassani Hassan, Aghamohammadi Asghar

机构信息

a Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center , Tehran University of Medical Sciences , Tehran , Iran.

b Department of Laboratory Medicine, Imam Hassan Mojtaba Hospital , Alborz University of Medical Sciences , Karaj , Iran.

出版信息

Expert Rev Clin Immunol. 2017 May;13(5):499-505. doi: 10.1080/1744666X.2017.1292131. Epub 2017 Feb 15.

Abstract

BACKGROUND

Ataxia telangiectasia (AT) is a primary immunodeficiency associated with recurrent infections. We aimed to investigate clinical and immunological classification in AT patients who suffer from a different spectrum of humoral immune defects.

METHODS

AT patients were categorized according to the ability of class switching and patients with hyper IgM (HIgM) profile were defined as class switching defect (CSD).

RESULTS

Serum immunoglobulin profile in 66 AT patients showed normal immunoglobulin level (22.8%), IgA deficiency (37.9%) and hypogammaglobulinemia (18.1%) in the majority of patients, while 21.2% had HIgM profile revealing CSD. CSD does not affect the frequency of infections, however, the frequency of lymphoproliferation (p < 0.001), and autoimmunity (p = 0.004) were significantly higher in this group. Neurologic symptoms in CSD patients are mild or appear after recurrent infections, therefore these patients were usually misdiagnosed as HIgM syndrome.

CONCLUSIONS

Although most of AT patients have reduced IgA levels or normal immunoglobulin levels, but a fraction of these patients may show CSD ensuing HIgM-profile. CSD poses affected individuals at higher risk of non-infectious complications.

摘要

背景

共济失调毛细血管扩张症(AT)是一种与反复感染相关的原发性免疫缺陷病。我们旨在研究患有不同类型体液免疫缺陷的AT患者的临床和免疫学分类。

方法

根据类别转换能力对AT患者进行分类,并将具有高IgM(HIgM)特征的患者定义为类别转换缺陷(CSD)。

结果

66例AT患者的血清免疫球蛋白谱显示,大多数患者免疫球蛋白水平正常(22.8%)、IgA缺乏(37.9%)和低丙种球蛋白血症(18.1%),而21.2%的患者具有HIgM特征,提示存在CSD。CSD不影响感染频率,然而,该组患者的淋巴细胞增殖频率(p < 0.001)和自身免疫频率(p = 0.004)显著更高。CSD患者的神经系统症状较轻或在反复感染后出现,因此这些患者通常被误诊为HIgM综合征。

结论

虽然大多数AT患者的IgA水平降低或免疫球蛋白水平正常,但其中一部分患者可能表现为CSD并伴有HIgM特征。CSD使受影响个体面临更高的非感染性并发症风险。

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