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阿达木单抗诱发的重症肌无力:基于病例的综述

Adalimumab-induced myasthenia gravis: case-based review.

作者信息

Pelechas Eleftherios, Memi Tereza, Markatseli Theodora E, Voulgari Paraskevi V, Drosos Alexandros A

机构信息

Department of Internal Medicine, Medical School, Rheumatology Clinic, University of Ioannina, 45110, Ioannina, Greece.

出版信息

Rheumatol Int. 2020 Nov;40(11):1891-1894. doi: 10.1007/s00296-020-04587-4. Epub 2020 Apr 22.

Abstract

Myasthenia gravis (MG) is an autoimmune disease characterised by the presence of acetylcholine receptor antibodies and by blocking the transmission of the signal in the neuromuscular junction causing muscle weakness. It can be associated with several autoimmune diseases and certain drugs, between them Etanercept an anti-tumour necrosis factor (TNF) agent. A 42-year-old woman with rheumatoid arthritis (RA) refractory to methotrexate, was treated with adalimumab (ADA), a human monoclonal antibody against the TNF, in a dosage scheme of 40 mg every 14 days subcutaneously. The patient responded well to ADA therapy with sustained remission for 18 months when she developed blurred vision and eyelid ptosis of the left eye. The diagnosis of ocular MG was made. ADA has been discontinued and she started a treatment with pyridostigmine showing an excellent response and complete remission within a 2-month period. This is the first report making an association of ADA and ocular MG. Thus, rheumatologists dealing with patients treated with TNF inhibitors should be aware of the possible development of neurological adverse events, among them MG.

摘要

重症肌无力(MG)是一种自身免疫性疾病,其特征是存在乙酰胆碱受体抗体,并通过阻断神经肌肉接头处的信号传递导致肌肉无力。它可与多种自身免疫性疾病和某些药物相关,其中包括抗肿瘤坏死因子(TNF)药物依那西普。一名42岁患有对甲氨蝶呤耐药的类风湿关节炎(RA)的女性,接受了阿达木单抗(ADA)治疗,这是一种抗TNF的人单克隆抗体,皮下注射剂量为每14天40mg。患者对ADA治疗反应良好,持续缓解18个月,之后出现左眼视力模糊和眼睑下垂。诊断为眼肌型重症肌无力。已停用ADA,她开始使用吡啶斯的明治疗,在2个月内显示出极佳反应并完全缓解。这是第一份将ADA与眼肌型重症肌无力相关联的报告。因此,治疗使用TNF抑制剂患者的风湿病学家应意识到可能发生的神经不良事件,其中包括重症肌无力。

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