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开始使用依库珠单抗作为难治性肌无力危象的抢救治疗。

Starting eculizumab as rescue therapy in refractory myasthenic crisis.

机构信息

Neurology Unit, University Hospital "San Giovanni di Dio e Ruggi d'Aragona", Largo Città di Ippocrate, 84100, Salerno, Italy.

Anesthesia and Intensive Care Unit, University Hospital "San Giovanni di Dio e Ruggi d'Aragona, Salerno, Italy.

出版信息

Neurol Sci. 2023 Oct;44(10):3707-3709. doi: 10.1007/s10072-023-06900-y. Epub 2023 Jun 12.

Abstract

INTRODUCTION

Myasthenia gravis is a long-lasting autoimmune neuromuscular disease caused by antibodies attacking the neuromuscular junction, which can result in muscle weakness, fatigue, and respiratory failure in severe cases. Myasthenic crisis is a life-threatening event that requires hospitalization and treatments with intravenous immunoglobulin or plasma exchange. We reported the case of an AChR-Ab-positive myasthenia gravis patient with refractory myasthenic crisis, in which starting eculizumab as rescue therapy led to a complete resolution of the acute neuromuscular condition.

CASE PRESENTATION

A 74-year-old man diagnosed with myasthenia gravis. ACh-receptor antibodies positivity comes to our observation for a recrudescence of symptoms, unresponsive to conventional rescue therapies. Due to the clinical worsening over the following weeks, the patient was admitted to intensive care unit, where he underwent therapy with eculizumab. About 5 days after the treatment, there was a significant and complete recovery of clinical condition with weaning-off from invasive ventilation and discharge to outpatient regimen, with reduction of steroid intake and biweekly maintenance with eculizumab.

DISCUSSION

Eculizumab, a humanized monoclonal antibody that inhibits complement activation, is now approved as treatment for refractory generalized myasthenia gravis with anti-AChR antibodies. The use of eculizumab in myasthenic crisis is still investigational, but this case report suggests that it may be a promising treatment option for patients with severe clinical condition. Ongoing clinical trials will be needed to further evaluate the safety and efficacy of eculizumab in myasthenic crisis.

摘要

介绍

重症肌无力是一种由抗体攻击神经肌肉接头引起的慢性自身免疫性疾病,可导致肌肉无力、疲劳和严重情况下的呼吸衰竭。肌无力危象是一种危及生命的事件,需要住院治疗,并采用静脉注射免疫球蛋白或血浆置换进行治疗。我们报告了一例 AChR-Ab 阳性的重症肌无力患者发生难治性肌无力危象,使用依库珠单抗作为挽救性治疗后,急性神经肌肉状况完全缓解。

病例介绍

一名 74 岁男性,被诊断为重症肌无力。AChR 抗体阳性来我院就诊,因症状复发且对常规挽救性治疗无反应。由于病情在接下来的几周内恶化,患者被收入重症监护病房,在那里接受了依库珠单抗治疗。治疗约 5 天后,患者的临床状况显著且完全恢复,成功撤下有创呼吸机并出院,开始门诊治疗,同时减少了激素的用量,每两周使用依库珠单抗进行维持治疗。

讨论

依库珠单抗是一种人源化单克隆抗体,可抑制补体激活,现已被批准用于治疗难治性全身型重症肌无力伴抗 AChR 抗体阳性。依库珠单抗在肌无力危象中的应用仍处于研究阶段,但本病例报告表明,它可能是一种治疗严重临床状况患者的有前途的治疗选择。需要进行更多的临床试验来进一步评估依库珠单抗在肌无力危象中的安全性和疗效。

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