Tebo A E, Szankasi P, Hillman T A, Litwin C M, Hill H R
Department of Pathology, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Clin Exp Immunol. 2006 Dec;146(3):427-32. doi: 10.1111/j.1365-2249.2006.03227.x.
Deafness is attributable to autoimmunity in a subset of adult patients with sensorineural hearing loss (SNHL) of unknown aetiology. To determine the roles of self-antigens in the pathogenesis of idiopathic SNHL, we analysed antibody responses to the inner ear-specific proteins, cochlin and beta-tectorin as well as the non-specific heat shock protein 70 (HSP70). Recombinant cochlin and beta-tectorin proteins were used in a qualitative Western blot assay for the detection of antigen-specific IgG antibodies in 58 patients with idiopathic SNHL and 28 healthy blood donors. In the same study cohort, we also used a Western blot assay to assess IgG antibody responses to the recombinant human HSP70. Of the 58 patient samples analysed, 19 tested positive to the HSP70, eight to cochlin and one to beta-tectorin, giving a prevalence of 33, 14 and 2%, respectively. Only one patient sample was reactive for HSP70, cochlin and beta-tectorin, seven of the remaining eight cochlin IgG antibody-positive samples were monospecific. Thus, cochlin-specific antibodies were observed predominantly in HSP70 IgG-negative patients demonstrating an additive value for testing this antibody response in patients with idiopathic SNHL.
在病因不明的成年感音神经性听力损失(SNHL)患者亚组中,耳聋可归因于自身免疫。为了确定自身抗原在特发性SNHL发病机制中的作用,我们分析了内耳特异性蛋白耳蜗蛋白和β-耳纤毛蛋白以及非特异性热休克蛋白70(HSP70)的抗体反应。重组耳蜗蛋白和β-耳纤毛蛋白用于定性蛋白质印迹分析,以检测58例特发性SNHL患者和28名健康献血者中的抗原特异性IgG抗体。在同一研究队列中,我们还使用蛋白质印迹分析来评估对重组人HSP70的IgG抗体反应。在分析的58份患者样本中,19份对HSP70检测呈阳性,8份对耳蜗蛋白呈阳性,1份对β-耳纤毛蛋白呈阳性,患病率分别为33%、14%和2%。只有一份患者样本对HSP70、耳蜗蛋白和β-耳纤毛蛋白有反应,其余8份耳蜗蛋白IgG抗体阳性样本中有7份是单特异性的。因此,耳蜗蛋白特异性抗体主要在HSP70 IgG阴性患者中观察到,这表明在特发性SNHL患者中检测这种抗体反应具有附加价值。