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自身免疫性感音神经性听力损失患者的T细胞对内耳抗原产生干扰素-γ 。

Interferon-gamma production to inner ear antigens by T cells from patients with autoimmune sensorineural hearing loss.

作者信息

Lorenz Robert R, Solares C Arturo, Williams Paul, Sikora John, Pelfrey Clara M, Hughes Gordon B, Tuohy Vincent K

机构信息

Department of Otolaryngology and Communicative Disorders, Cleveland Clinic Foundation, 44195, Cleveland, OH, USA.

出版信息

J Neuroimmunol. 2002 Sep;130(1-2):173-8. doi: 10.1016/s0165-5728(02)00190-x.

Abstract

Autoimmune sensorineural hearing loss (ASNHL) typically produces bilateral rapidly progressive loss of hearing over a few days or weeks, but may also produce sudden loss over a few hours. The diagnosis is made by excluding ototoxicity, systemic disease, and other factors that mimic ASNHL and by showing a therapeutic response to corticosteroid treatment. Antibody production and T-cell proliferative responses to inner ear antigens have been implicated in the etiopathogenesis of ASNHL. In the current study, we have extended these autoimmune investigations by determining the frequencies of inner ear specific IFN-gamma producing T cells in peripheral blood mononuclear cells (PBMC) from ASNHL patients and from age- and sex-matched control subjects. ELISPOT analysis showed that 25% of ASNHL patients have significant increased frequencies of inner ear specific IFN-gamma producing T cells in their PBMC. All control subjects were relatively unresponsive. Our results implicate inner ear specific IFN-gamma producing proinflammatory T cells in the pathogenesis of ASNHL.

摘要

自身免疫性感音神经性听力损失(ASNHL)通常在几天或几周内导致双侧听力迅速进行性丧失,但也可能在几小时内突然丧失。通过排除耳毒性、全身性疾病以及其他模仿ASNHL的因素,并显示对皮质类固醇治疗的治疗反应来做出诊断。抗体产生以及对内耳抗原的T细胞增殖反应与ASNHL的发病机制有关。在本研究中,我们通过测定ASNHL患者以及年龄和性别匹配的对照受试者外周血单核细胞(PBMC)中产生内耳特异性干扰素-γ的T细胞频率,扩展了这些自身免疫性研究。酶联免疫斑点分析显示,25%的ASNHL患者其PBMC中产生内耳特异性干扰素-γ的T细胞频率显著增加。所有对照受试者反应相对较弱。我们的结果表明,产生内耳特异性干扰素-γ的促炎性T细胞参与了ASNHL的发病机制。

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