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进行性多灶性白质脑病

Progressive multifocal leukoencephalopathy.

作者信息

Berger Joseph R

机构信息

Department of Neurology, University of Kentucky College of Medicine, Kentucky Clinic L-445, 740 S. Limestone Street, Lexington, KY 40536-0284, USA.

出版信息

Curr Neurol Neurosci Rep. 2007 Nov;7(6):461-9. doi: 10.1007/s11910-007-0072-9.

Abstract

Progressive multifocal leukoencephalopathy (PML) was a rare disease until the advent of the HIV/AIDS pandemic. Recent interest in the disorder has been spurred by its appearance in patients treated with the monoclonal antibodies natalizumab and rituximab. Unless the accompanying underlying immune deficit can be reversed, PML typically progresses to death fairly rapidly. Treatment directed against the JC virus has been unhelpful, but an increased understanding of disease pathogenesis may result in effective therapeutic strategies.

摘要

在艾滋病大流行出现之前,进行性多灶性白质脑病(PML)是一种罕见疾病。近期,由于该疾病在接受那他珠单抗和利妥昔单抗这两种单克隆抗体治疗的患者中出现,引发了人们对它的关注。除非伴随的潜在免疫缺陷能够得到逆转,否则PML通常会相当迅速地发展至死亡。针对JC病毒的治疗并无效果,但对疾病发病机制的进一步了解可能会带来有效的治疗策略。

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