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阿仑单抗在视神经脊髓炎谱系障碍中的应用:简短病例系列

Alemtuzumab use in neuromyelitis optica spectrum disorders: a brief case series.

作者信息

Azzopardi Laura, Cox Amanda L, McCarthy Claire L, Jones Joanne L, Coles Alasdair J

出版信息

J Neurol. 2016 Jan;263(1):25-9. doi: 10.1007/s00415-015-7925-y.

Abstract

Alemtuzumab is an anti-CD52 monoclonal antibody recently licensed for use in relapsing-remitting multiple sclerosis. Here, we report our experience of its use in neuromyelitis optica (NMO) spectrum disorders. A retrospective case review of patients treated with alemtuzumab in Cambridge, UK, was conducted to identify those who fulfil the criteria for NMO spectrum disorder. Three cases were identified. Case 1, 9-year-old female, presented with transverse myelitis and bilateral optic neuritis,with one lower medullary and several longitudinally extensive cord lesions. Despite immunosuppression including two courses of alemtuzumab, she continued to relapse, was wheelchair bound and registered blind by age 12, and died at age 18. Case 2, 41-year-old female, presented with bilateral optic neuritis and transverse myelitis with longitudinally extensive cervical cord lesions. Despite three courses of alemtuzumab, she had five relapses with visual impairment and new cord lesions. She later developed tumefactive white matter lesions and died aged 51.Case 3, 31-year-old female, presented with transverse myelitis with longitudinally extensive cervical cord lesions and positive aquaporin-4 antibody. After one course of alemtuzumab, she relapsed with 4 episodes of myelitis with new enhancing lesions and accumulating disability. She became relapse free after rituximab and mycophenolate mofetil. From this case series, we conclude that alemtuzumab failed to prevent disabling relapses and poor outcome in NMO. We hypothesise that rituximab is more effective, as in case 3, because it causes much more prolonged B lymphocyte depletion than alemtuzumab. We therefore caution against the use of alemtuzumab in NMO.

摘要

阿仑单抗是一种抗CD52单克隆抗体,最近被批准用于复发缓解型多发性硬化症。在此,我们报告其在视神经脊髓炎(NMO)谱系障碍中的应用经验。我们对英国剑桥接受阿仑单抗治疗的患者进行了回顾性病例分析,以确定符合NMO谱系障碍标准的患者。共识别出3例。病例1为一名9岁女性,表现为横贯性脊髓炎和双侧视神经炎,伴有一个延髓下部和几个纵向广泛的脊髓病变。尽管进行了包括两个疗程阿仑单抗在内的免疫抑制治疗,但她仍持续复发,12岁时需依靠轮椅行动且失明,并于18岁去世。病例2为一名41岁女性,表现为双侧视神经炎和横贯性脊髓炎,伴有纵向广泛的颈髓病变。尽管接受了三个疗程的阿仑单抗治疗,但她仍复发了5次,伴有视力障碍和新的脊髓病变。她后来出现了瘤样白质病变,并于51岁去世。病例3为一名31岁女性,表现为横贯性脊髓炎,伴有纵向广泛的颈髓病变,水通道蛋白-4抗体呈阳性。经过一个疗程的阿仑单抗治疗后,她复发了4次脊髓炎,出现了新的强化病变并逐渐出现残疾。在使用利妥昔单抗和霉酚酸酯后,她不再复发。从这个病例系列中,我们得出结论,阿仑单抗未能预防NMO患者出现致残性复发和不良预后。我们推测利妥昔单抗更有效,如病例3所示,因为它导致B淋巴细胞耗竭的时间比阿仑单抗长得多。因此,我们告诫不要在NMO中使用阿仑单抗。

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