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与γ干扰素产生缺陷相关的IgG2缺乏症;与常见可变免疫缺陷的比较。

IgG2 deficiency associated with defects in production of interferon-gamma; comparison with common variable immunodeficiency.

作者信息

Inoue R, Kondo N, Kobayashi Y, Fukutomi O, Orii T

机构信息

Department of Pediatrics, Gifu University School of Medicine, Japan.

出版信息

Scand J Immunol. 1995 Feb;41(2):130-4. doi: 10.1111/j.1365-3083.1995.tb03544.x.

Abstract

We report a novel mechanism of IgG2 deficiency. Several investigators have reported patients with IgG subclass deficiencies due to homozygous deletion of immunoglobulin heavy chain constant region genes. However, it is unclear what mechanism is responsible for IgG subclass deficiency in cases where no gene deletions have been detected and which are accompanied by recurrent infections due to aberrant immunoregulation. In the present study, we have focused our attention on production by peripheral blood mononuclear cells (PBMCs) of interferon-gamma (IFN-gamma), which is known to induce IgG2 expression. PBMCs from four patients with IgG2 deficiency and their families were studied. Mitogeninduced IFN-gamma production by PBMCs was decreased in all of the patients, although the proliferative responses of PBMCs and the percentages of CD3, CD4, and CD8 T cell subsets were not decreased. IgG2 production by PBMCs was restored upon addition of IFN-gamma and mitogen to the PBMCs of the patients with IgG2 deficiency though it was not restored in the patients with common variable immunodeficiency. We conclude that defects in production of IFN-gamma play an important role in IgG2 deficiency.

摘要

我们报告了一种新型的IgG2缺乏机制。几位研究者报道过因免疫球蛋白重链恒定区基因纯合缺失导致IgG亚类缺陷的患者。然而,在未检测到基因缺失且因免疫调节异常而伴有反复感染的病例中,导致IgG亚类缺陷的机制尚不清楚。在本研究中,我们将注意力集中于外周血单个核细胞(PBMC)产生的γ干扰素(IFN-γ),已知其可诱导IgG2表达。我们研究了4例IgG2缺乏患者及其家族成员的PBMC。尽管PBMC的增殖反应以及CD3、CD4和CD8 T细胞亚群的百分比未降低,但所有患者的PBMC经丝裂原诱导产生的IFN-γ均减少。向IgG2缺乏患者的PBMC中添加IFN-γ和丝裂原后,PBMC的IgG2产生得以恢复,不过在常见变异型免疫缺陷患者中未恢复。我们得出结论,IFN-γ产生缺陷在IgG2缺乏中起重要作用。

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