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[骨骼肌系统的自身免疫性疾病。重症肌无力和多发性肌炎的免疫发病机制(作者译)]

[Auto-immune diseases of the skeletal muscle-system. Immune-pathogenetic mechanisms in myasthenia gravis and polymyositis (author's transl)].

作者信息

Kalden J R

出版信息

Immun Infekt. 1975 Jul;3(3):100-15.

PMID:1184099
Abstract

Intensive clinical as well as experimental research over the past decade in the pathogenesis of myasthenia gravis suggest the imporatance of involved immunological reactions. The thymus as well as the muscle endplates appeare to be possible target organs of autoaggressive reactions, although the real trigger mechanismus of autoimmune reactivity are not yet understood. Different pathogenetic hypothesis for myasthenia gravis are discussed. Regarding the pathogenesis of polymyositis more direct evidence for the possible involvement of viruses are offered by electronmicroscopy. Beside clinical and neurological findings, immunoserological data provide the most important facts for the diagnosis and differential diagnosis of myasthenia gravis and polymyositis.

摘要

在过去十年中,针对重症肌无力发病机制的深入临床及实验研究表明免疫反应的重要性。胸腺以及肌肉终板似乎是自身攻击性反应的潜在靶器官,尽管自身免疫反应的真正触发机制尚未明确。本文讨论了重症肌无力不同的发病机制假说。关于多发性肌炎的发病机制,电子显微镜检查为病毒可能参与其中提供了更直接的证据。除了临床和神经学检查结果外,免疫血清学数据为重症肌无力和多发性肌炎的诊断及鉴别诊断提供了最重要的依据。

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