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快速进展性感音神经性听力损失患者的内耳自身抗体

Inner ear autoantibodies in patients with rapidly progressive sensorineural hearing loss.

作者信息

Harris J P, Sharp P A

机构信息

Division of Otolaryngology-Head and Neck Surgery, University of California, San Diego Medical Center 92103.

出版信息

Laryngoscope. 1990 May;100(5):516-24. doi: 10.1288/00005537-199005000-00015.

Abstract

Recognition of immune-mediated sensorineural deafness that responds to immunosuppressive therapy has led to a search for a diagnostic assay to identify inner ear autoantibodies. Without a confirmed diagnosis of autoimmune disease, many patients have undergone inappropriate immunosuppressive treatment or developed irreversible inner ear damage. Serum from patients with progressive sensorineural hearing loss (n = 54), ulcerative colitis (N = 5), normal controls (N = 14), and animals with experimental autoimmune sensorineural hearing loss (EASNHL) were analyzed by Western blot against fresh bovine inner ear antigen preparations. The hearing loss group (19 [35%]) showed a single-or double-band migrating at 68,000 molecular weight (MW), differing from the normal group (1 of 14 [7%]) which showed a similar band (P = .031). Upon analysis by two-dimensional gel electrophoresis both the EASNHL guinea pigs and a patient reacted against identical components of inner ear antigen. These results suggest an autoimmune basis for disease in patients reacting against the 68,000 MW antigen.

摘要

对免疫抑制疗法有反应的免疫介导性感音神经性聋的认识,促使人们寻找一种诊断检测方法来识别内耳自身抗体。在没有确诊自身免疫性疾病的情况下,许多患者接受了不适当的免疫抑制治疗,或出现了不可逆的内耳损伤。采用针对新鲜牛内耳抗体制剂的蛋白质印迹法,对进行性感音神经性听力损失患者(n = 54)、溃疡性结肠炎患者(N = 5)、正常对照者(N = 14)以及实验性自身免疫性感音神经性听力损失(EASNHL)动物的血清进行了分析。听力损失组(19例[35%])显示出一条或两条迁移至分子量(MW)68,000处的条带,与正常组(14例中的1例[7%])显示出类似条带不同(P = 0.031)。通过二维凝胶电泳分析,EASNHL豚鼠和一名患者均对相同的内耳抗原成分产生反应。这些结果提示,对68,000 MW抗原产生反应的患者的疾病存在自身免疫基础。

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