Immunology Department, Barts Health NHS Trust, London, UK.
Clin Exp Immunol. 2013 Feb;171(2):195-200. doi: 10.1111/cei.12010.
Common variable immunodeficiency (CVID) is the most common severe primary immunodeficiency, but the pathology of this condition is poorly understood. CVID involves a defect in the production of immunoglobulin from B cells, with a subsequent predisposition to infections. Approximately 10-20% of cases are inherited, but even in families with a genetic defect the penetrance is far from complete. A classification system for CVID has been suggested (EUROclass) based on B cell immunophenotyping, but it has not been shown that altered B cell immunophenotype is not a consequence of the complications and treatment of CVID. This study compares the EUROclass B cell immunophenotype of CVID patients (n = 30) with suitable disease controls with bronchiectasis (n = 11), granulomatous disease (Crohn's disease) (n = 9) and neurological patients on immunoglobulin treatment (n = 6). The results of this study correlate with previous literature, that alterations in B cell immunophenotype are associated strongly with CVID. Interestingly, three of the 11 bronchiectasis patients without known immunodeficiency had an altered B cell immunophenotype, suggesting the possibility of undiagnosed immunodeficiency, or that bronchiectasis may cause a secondary alteration in B cell immunophenotype. This study showed a significant difference in B cell immunophenotype between CVID patients compared to disease control groups of granulomatous disease and immunoglobulin treatment. This suggests that granulomatous disease (in Crohn's disease) and immunoglobulin treatment (for chronic neurological conditions) are not causal of an altered B cell immunophenotype in these control populations.
普通变异性免疫缺陷症(CVID)是最常见的严重原发性免疫缺陷症,但该病症的病理仍知之甚少。CVID 涉及 B 细胞产生免疫球蛋白的缺陷,随后易发生感染。约 10-20%的病例为遗传性,但即使在存在遗传缺陷的家族中,外显率也远未达到完全。已经提出了一种基于 B 细胞免疫表型的 CVID 分类系统(EUROclass),但尚未表明改变的 B 细胞免疫表型不是 CVID 的并发症和治疗的结果。本研究比较了 30 例 CVID 患者(n=30)的 EUROclass B 细胞免疫表型与支气管扩张症(n=11)、肉芽肿性疾病(克罗恩病)(n=9)和接受免疫球蛋白治疗的神经科患者(n=6)的合适疾病对照。该研究的结果与先前的文献相符,即 B 细胞免疫表型的改变与 CVID 密切相关。有趣的是,11 例无已知免疫缺陷的支气管扩张症患者中有 3 例存在 B 细胞免疫表型改变,这表明可能存在未诊断的免疫缺陷,或者支气管扩张症可能导致 B 细胞免疫表型的继发性改变。本研究显示,与肉芽肿性疾病和免疫球蛋白治疗的疾病对照组相比,CVID 患者的 B 细胞免疫表型存在显著差异。这表明,在这些对照组中,肉芽肿性疾病(在克罗恩病中)和免疫球蛋白治疗(用于慢性神经疾病)不是这些对照组中 B 细胞免疫表型改变的原因。