Department of Neurology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA.
J Neurovirol. 2008 Nov;14(6):569-73. doi: 10.1080/13550280802304753.
We report here a case of progressive tumefactive inflammatory central nervous system (CNS) demyelinating disease in a human immunodeficiency virus (HIV)-seropositive patient treated with highly active antiretroviral therapy (HAART). Biopsy revealed diffuse macrophage and perivascular T-lymphocytic infiltrates with severe demyelination and relative axonal sparing. The disease progressed in a centrifugal fashion, to involve bihemispheric cerebral white matter, with subsequent central necrotic changes and atrophy. Treatment with HAART was discontinued, and inflammatory disease was treated with subcutaneous interferon (IFN)beta-1a. Massive brain edema was controlled with courses of intravenous corticosteroids. Following fulminant monophasic disease, the patient stabilized with no evidence of disease progression over long-term follow up. We propose that immune response reconstituted by HAART can unmask an autoimmune response in susceptible individuals, analogous to the enhanced immune response to the preexisting acquired immunodeficiency syndrome (AIDS) opportunistic infections. Therapeutic options are considered.
我们在此报告一例人类免疫缺陷病毒(HIV)血清阳性患者在接受高效抗逆转录病毒治疗(HAART)后发生进行性肿块状炎症性中枢神经系统(CNS)脱髓鞘疾病。活检显示弥漫性巨噬细胞和血管周围 T 淋巴细胞浸润,伴有严重脱髓鞘和相对轴索保留。疾病呈离心性进展,累及大脑两半球白质,随后出现中央坏死性改变和萎缩。停用 HAART 治疗,用皮下干扰素(IFN)β-1a 治疗炎症性疾病。大剂量皮质类固醇静脉滴注控制脑水肿。在单相暴发性疾病后,患者在长期随访中无疾病进展的证据而稳定。我们提出,HAART 重建的免疫反应可能会使易感个体暴露出自身免疫反应,类似于对先前存在的获得性免疫缺陷综合征(AIDS)机会性感染的增强免疫反应。考虑了治疗选择。