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一例使用贝利尤单抗治疗的狼疮患者发生进行性多灶性白质脑病。

A case of progressive multifocal leukoencephalopathy in a lupus patient treated with belimumab.

作者信息

Fredericks C A, Kvam K A, Bear J, Crabtree G S, Josephson S A

机构信息

University of California San Francisco, San Francisco, USA

University of California San Francisco, San Francisco, USA.

出版信息

Lupus. 2014 Jun;23(7):711-3. doi: 10.1177/0961203314524292. Epub 2014 Feb 14.

Abstract

Belimumab is a monoclonal antibody against soluble B-lymphocyte stimulator, an essential growth factor for B-cell maturation and activation, which was approved by the US FDA in 2011 for patients with active autoantibody-positive systemic lupus erythematosus (SLE) who have failed standard treatment. Here we present the case of a 40-year-old woman with SLE diagnosed with progressive multifocal leukoencephalopathy (PML) on belimumab. After a total of 10 infusions of belimumab, from August 2012 through April 2013, in April 2013 she developed progressive neurologic decline with episodic dystonia and autonomic symptoms. Her imaging showed multifocal, confluent regions of T2 hyperintensity in the white matter bilaterally, and CSF JCV PCR returned positive. Based on the patient's clinically mild SLE and the timing of symptom onset, belimumab likely played a key role in the development of PML. Trials of belimumab for other autoimmune diseases are ongoing; as applications for this novel drug broaden, careful monitoring for this potentially fatal adverse effect is warranted.

摘要

贝利尤单抗是一种针对可溶性B淋巴细胞刺激因子的单克隆抗体,该因子是B细胞成熟和激活所必需的生长因子。2011年,美国食品药品监督管理局(FDA)批准贝利尤单抗用于治疗标准治疗无效的活动性自身抗体阳性系统性红斑狼疮(SLE)患者。在此,我们报告一例40岁SLE女性患者,在使用贝利尤单抗治疗期间被诊断为进行性多灶性白质脑病(PML)。从2012年8月至2013年4月,该患者共接受了10次贝利尤单抗输注,2013年4月,她出现了进行性神经功能衰退,并伴有发作性肌张力障碍和自主神经症状。其影像学检查显示双侧白质出现多灶性、融合性T2高信号区域,脑脊液JCV PCR检测呈阳性。基于该患者临床症状较轻的SLE以及症状出现的时间,贝利尤单抗可能在PML的发生中起了关键作用。目前正在进行贝利尤单抗用于其他自身免疫性疾病的试验;随着这种新药应用范围的扩大,有必要对这种潜在致命的不良反应进行密切监测。

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