Department of Neurology, Yale University School of Medicine, 40 Temple Street, Suite 6C, New Haven, Connecticut 06510, USA.
Muscle Nerve. 2010 Mar;41(3):375-8. doi: 10.1002/mus.21521.
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.
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。