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进行性多灶性白质脑病

Progressive Multifocal Leukoencephalopathy.

作者信息

Berger JR

机构信息

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

出版信息

Curr Treat Options Neurol. 2000 Jul;2(4):361-368. doi: 10.1007/s11940-000-0053-7.

Abstract

Before embarking on experimental therapies for progressive multifocal leukoencephalopathy (PML), the diagnosis needs to be unequivocally established. Improving the underlying immunodeficiency state is the best initial approach to the management of PML. Immunosuppressive therapies should be discontinued when feasible. In the patient with AIDS, highly active antiretroviral therapy should be administered; this appears to prolong survival. At present, no therapy has been demonstrated to be effective in a well-designed prospective trial. Cytosine arabinoside, which has demonstrated efficacy in vitro against JC virus, has not been effective when administered intravenously or intrathecally to patients with AIDS and PML. The failure of regimens employing cytosine arabinoside in PML may have been the consequence of inadequate penetration of the drug to sites of infection in the brain. Other drugs with established in vitro activity against JC virus, such as topoisomerase and camptothecin, are poorly tolerated. The use of cidofovir in patients with AIDS and PML remains anecdotal, although it is currently under investigation. Interferon alfa may improve survival in patients with AIDS and PML and may have general applicability to PML regardless of the cause of the underlying immunodeficient state. Approximately 7% to 9% of patients with PML demonstrate prolonged survival (>12 months) and associated improvement in clinical and radiographic abnormalities in the absence of specific therapy. In patients with AIDS-related PML, prolonged survival correlates with PML as the presenting manifestation of AIDS, higher CD4 T-lymphocyte counts, and contrast enhancement of PML lesions on radiographic imaging. A brisk inflammatory response may also be associated with improved survival. The increased understanding of the pathophysiology of JC virus provides hope for the development of curative strategies. The growing number of persons affected with PML has allowed the organization of carefully designed therapeutic trials to address this issue.

摘要

在开始针对进行性多灶性白质脑病(PML)的实验性治疗之前,必须明确诊断。改善潜在的免疫缺陷状态是PML治疗的最佳初始方法。可行时应停用免疫抑制疗法。对于艾滋病患者,应给予高效抗逆转录病毒疗法;这似乎可延长生存期。目前,在精心设计的前瞻性试验中,尚无治疗方法被证明有效。阿糖胞苷在体外对JC病毒有疗效,但静脉或鞘内给药于艾滋病合并PML患者时却无效。PML中使用阿糖胞苷的治疗方案失败可能是因为药物对脑部感染部位的渗透不足。其他在体外对JC病毒有活性的药物,如拓扑异构酶和喜树碱,效果不佳。尽管目前正在研究,但西多福韦在艾滋病合并PML患者中的应用仍属个案报道。干扰素α可能会提高艾滋病合并PML患者的生存率,并且可能普遍适用于PML,无论潜在免疫缺陷状态的病因如何。在没有特定治疗的情况下,约7%至9%的PML患者生存期延长(>12个月),临床和影像学异常也有所改善。在艾滋病相关PML患者中,生存期延长与PML作为艾滋病的首发表现、较高的CD4 T淋巴细胞计数以及影像学检查中PML病灶的强化有关。活跃的炎症反应也可能与生存期改善有关。对JC病毒病理生理学认识的增加为治愈策略的开发带来了希望。受PML影响的人数不断增加,这使得能够组织精心设计的治疗试验来解决这一问题。

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