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[利妥昔单抗治疗复发性视神经脊髓炎失败:病例报告及两年前瞻性随访]

[Failure of rituximab in relapsing neuromyelitis optica: case report with two-year prospective follow-up].

作者信息

Cassinotto C, Joux J, Chausson N, Smadja D, Cabre P

机构信息

Service de neurologie, CHU La Meynard, 97200 Fort-de-France, Martinique, France.

出版信息

Rev Neurol (Paris). 2008 Apr;164(4):394-7. doi: 10.1016/j.neurol.2007.10.009. Epub 2008 Feb 21.

Abstract

Neuromyelitis optica (Devic's disease, NMO) is an inflammatory disease of the central nervous system preferentially involving the spinal cord and optic nerves in either a monophasic or relapsing-remitting course. B-cell induced pathogenesis was recently described for NMO. Rituximab is a chimeric monoclonal antibody directed against the CD20 antigen, which causes depletion of B-cells. Rituximab might be effective in treatment of NMO. We report the two-year clinicoradiological and biological follow-up data from a patient included in July 2005 in a prospective trial of rituximab for severe NMO refractory to immunosuppressant therapy. Blood B-cell depletion after rituximab induction was maintained for 10 months. Seven attacks occurred during a two-year follow-up. EDSS increased from 7.0 to 8.0. Left visual acuity decreased from 20/20 degrees to 20/60 degrees. Spinal cord atrophy worsened.

摘要

视神经脊髓炎(德维克病,NMO)是一种中枢神经系统炎性疾病,在单相或复发-缓解病程中优先累及脊髓和视神经。最近描述了NMO由B细胞介导的发病机制。利妥昔单抗是一种针对CD20抗原的嵌合单克隆抗体,可导致B细胞耗竭。利妥昔单抗可能对NMO治疗有效。我们报告了一名于2005年7月纳入利妥昔单抗治疗严重免疫抑制剂难治性NMO前瞻性试验患者的两年临床放射学和生物学随访数据。利妥昔单抗诱导后血液B细胞耗竭持续了10个月。在两年随访期间发生了7次发作。扩展残疾状态量表(EDSS)从7.0增加到8.0。左眼视力从20/20降至20/60。脊髓萎缩加重。

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