Department of Neurology, University of Kentucky College of Medicine, 740 S. Limestone St., Lexington, KY, 40515, USA.
Curr Infect Dis Rep. 2011 Aug;13(4):380-6. doi: 10.1007/s11908-011-0196-6.
Progressive multifocal leukoencephalopathy (PML) is a rare but devastating neurologic disease that affects the immunosuppressed population. The etiologic agent is a polyomavirus, JC virus-a double-stranded DNA virus with a high prevalence of infection globally. PML is believed to occur from reactivation of the latent virus infection caused by immunosuppression. After 1980, a dramatic increase in the incidence and prevalence of PML was attributed to the HIV/AIDS pandemic, with a decline noted after the introduction of highly active antiretroviral treatment (HAART). Newer populations are being added to the risk pool for the development of PML with the introduction of biologic agents that target specific arms of the immune system. Natalizumab and efalizumab seem to have the highest risk for the development of PML, although PML can develop with the other biologic agents. As more patients are treated with these agents, effective risk mitigation strategies are needed to prevent PML.
进行性多灶性白质脑病(PML)是一种罕见但严重的神经系统疾病,影响免疫抑制人群。病原体是一种多瘤病毒,即 JC 病毒——一种具有全球高感染率的双链 DNA 病毒。人们认为 PML 是由免疫抑制引起的潜伏病毒感染重新激活引起的。自 1980 年以来,随着 HIV/AIDS 大流行的出现,PML 的发病率和患病率显著增加,在引入高效抗逆转录病毒治疗(HAART)后有所下降。随着针对免疫系统特定分支的生物制剂的引入,新的人群被纳入 PML 发病风险池。虽然 PML 也可能在其他生物制剂中发生,但那那他珠单抗和依法珠单抗似乎具有发生 PML 的最高风险。随着越来越多的患者接受这些药物治疗,需要采取有效的风险缓解策略来预防 PML。