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利妥昔单抗治疗难治性重症肌无力。

Rituximab in the management of refractory myasthenia gravis.

机构信息

Department of Neurology, Yale University School of Medicine, 40 Temple Street, Suite 6C, New Haven, Connecticut 06510, USA.

出版信息

Muscle Nerve. 2010 Mar;41(3):375-8. doi: 10.1002/mus.21521.

Abstract

Myasthenia gravis (MG) is an immune-mediated disorder with a variable response to treatment. In this study, patients with refractory MG who were treated with rituximab were identified. A review of patients referred to the Yale Neuromuscular Clinic was performed. Patients with refractory MG who were treated with rituximab were reviewed for response to treatment. Patients who had muscle-specific kinase (MuSK(+)) or acetylcholine receptor (AChR(+)) antibodies were included. Six patients were identified who met the criteria described. All patients tolerated rituximab without side effects and had a reduced need for immunosuppressants and/or improvement in clinical function. Patients with refractory MG appeared to respond to rituximab in this small, retrospective study. This result suggests that a larger, prospective trial is indicated.

摘要

重症肌无力(MG)是一种免疫介导的疾病,其治疗反应具有可变性。本研究鉴定了接受利妥昔单抗治疗的难治性 MG 患者。对耶鲁神经肌肉诊所转介的患者进行了回顾。对接受利妥昔单抗治疗的难治性 MG 患者进行了治疗反应评估。包括具有肌肉特异性激酶(MuSK(+)) 或乙酰胆碱受体(AChR(+)) 抗体的患者。符合描述标准的 6 名患者被确定。所有患者均耐受利妥昔单抗,无副作用,且减少了对免疫抑制剂的需求和/或临床功能改善。在这项小型回顾性研究中,难治性 MG 患者似乎对利妥昔单抗有反应。该结果表明,需要进行更大规模的前瞻性试验。

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