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重症肌无力和多发性肌炎中对肌肉和胸腺的迟发型超敏反应。

Delayed hypersensitivity to muscle and thymus in myasthenia gravis and polymyositis.

作者信息

Goust J M, Castaigne A, Moulias R

出版信息

Clin Exp Immunol. 1974 Sep;18(1):39-47.

Abstract

Delayed hypersensitivity reactions appear to be important in the two main muscular human diseases involving autoimmune anomalies. Using the leucocyte migration test (LMT), a significant abnormality was detected in twelve out of fourteen polymyositis (PM) patients, and in forty out of forty-six myasthenics, in the presence of muscle antigens. No abnormal reactions in the presence of monkey thymus in the LMT were observed amongst the PM patients, as opposed to twenty-one abnormal reactions out of forty-two myasthenics. Secretion of migration inhibition factor (MIF) in the presence of muscular antigens is in accordance with what is known about hypersensitivity reactions during the course of polymyositis. In myasthenia gravis (MG), delayed hypersensitivity to muscle antigens was found to be frequent, and this also applies to thymic antigens, which are considered important in this disease. The role of the T lymphocytes in the neuromuscular junction still remains hypothetical.

摘要

迟发型超敏反应在涉及自身免疫异常的两种主要人类肌肉疾病中似乎很重要。使用白细胞迁移试验(LMT),在14例多发性肌炎(PM)患者中有12例以及46例肌无力患者中有40例在存在肌肉抗原的情况下检测到明显异常。在LMT中,PM患者在存在猴胸腺的情况下未观察到异常反应,而42例肌无力患者中有21例出现异常反应。在存在肌肉抗原的情况下迁移抑制因子(MIF)的分泌与多发性肌炎病程中已知的超敏反应一致。在重症肌无力(MG)中,发现对肌肉抗原的迟发型超敏反应很常见,这也适用于胸腺抗原,胸腺抗原在该疾病中被认为很重要。T淋巴细胞在神经肌肉接头中的作用仍然是假设性的。

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