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[内耳的免疫病理学]

[Immunopathology of the inner ear].

作者信息

Arnold W, Altermatt H J, Gebbers J O, Pfaltz C R

出版信息

Laryngol Rhinol Otol (Stuttg). 1985 Jan;64(1):1-8.

PMID:3881636
Abstract

Immunologically mediated tissue lesions or functional disturbances can result from immune responses either to foreign antigens or autoantigenic constituents. Before a disease or a functional disorder can be called an (auto)immune disease, it must be established that immunological processes are involved in its etiology and/or pathogenesis. After reviewing the available data on immunology and on research on immunobiology of the inner ear, as well as clinical observations on disorders of the inner ear of possibly immunological origin, an attempt is made to determine whether (auto)immunopathology can be assumed in some patients with sensineural hearing loss. In patients with disorders presently recognized as autoimmune diseases, no hearing loss has been described so far. However, serum antibodies can be found via the indirect immunofluorescence method in some patients having functional disorders of the inner ear. These serum antibodies interact with normal human inner ear tissue. However, as long as immunopathological mechanisms have not been confirmed, these disorders should merely be called "diseases with autoimmune markers." It has been shown in animal experiments that the production of autoantibodies against inner ear components is associated with morphological and functional changes of the inner ear. The human endolymphatic sac releases secretory IgA into the lumen. Its epithelium contains (intraepithelial) lymphocytes, whereas lymphocytes, plasma cells (IgA, IgG) and macrophages occur in the perisaccular region. In this manner, the inner ear has its own immune system, which can possibly react independently of the systemic immune system.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

免疫介导的组织损伤或功能紊乱可由针对外来抗原或自身抗原成分的免疫反应引起。在一种疾病或功能障碍被称为(自身)免疫性疾病之前,必须确定免疫过程参与了其病因和/或发病机制。在回顾了有关免疫学和内耳免疫生物学研究的现有数据,以及对可能具有免疫源性的内耳疾病的临床观察之后,我们试图确定在一些感音神经性听力损失患者中是否可以假定存在(自身)免疫病理学。在目前被认为是自身免疫性疾病的患者中,迄今为止尚未有听力损失的描述。然而,通过间接免疫荧光法可以在一些患有内耳功能障碍的患者中发现血清抗体。这些血清抗体与正常人内耳组织相互作用。然而,只要免疫病理机制尚未得到证实,这些疾病就只能被称为“具有自身免疫标志物的疾病”。动物实验表明,针对内耳成分产生自身抗体与内耳的形态和功能变化有关。人内淋巴囊将分泌性IgA释放到腔内。其上皮含有(上皮内)淋巴细胞,而淋巴细胞、浆细胞(IgA、IgG)和巨噬细胞出现在囊周区域。通过这种方式,内耳有其自身的免疫系统,它可能独立于全身免疫系统做出反应。(摘要截选至250词)

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