Neuropathology and pathogenesis of HIV encephalopathies.

Acta histochemica. Supplementband Pub Date : 1992-01-01
O D Wiestler, S L Leib, O Brüstle, H Spiegel, P Kleihues
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Abstract

The nervous system is frequently affected in patients with the acquired immune deficiency syndrome (AIDS). In addition to opportunistic CNS infections and cerebral lymphomas, approx. 20% of the patients develop HIV-associated encephalopathies. Two major histopathological manifestations are observed. HIV leukoencephalopathy (progressive diffuse leukoencephalopathy) is characterized by a diffuse loss of myelin in the deep white matter of the cerebral and cerebellar hemispheres, with scattered multinucleated giant cells and microglia but scarce or absent inflammatory reaction. HIV encephalitis (multinucleated giant cell encephalitis) is associated with accumulations of multinucleated giant cells, inflammatory reaction and often focal necroses. In some patients, both patterns may overlap. In order to identify the HIV genome in the CNS, brain tissue from 27 patients was analyzed for the presence of HIV gag sequences using the polymerase chain reaction (PCR) and primers encoding a 109 base pair segment of the gag gene. Amplification of HIV gag succeeded in all 5 patients with clinical and histopathological evidence for HIV encephalopathy but was negative in the 20 AIDS patients with opportunistic bacterial, parasitic and/or viral infections or with cerebral lymphomas. These results strongly suggest that the evolution of histopathologically recognizable HIV-encephalopathies closely correlates with the presence and/or tissue concentration of HIV. Since there were no cases with amplified HIV DNA in the absence of HIV-associated tissue lesions, we conclude that harboring and replication of HIV in the CNS rapidly causes corresponding clinical and morphological changes of HIV-associated encephalopathies. In two children with severe HIV encephalomyelitis, large amounts of HIV gag and env transcripts were detected in affected areas of the brain and spinal cord by in situ hybridization.(ABSTRACT TRUNCATED AT 250 WORDS)

HIV脑病的神经病理学和发病机制。
获得性免疫缺陷综合征(AIDS)患者的神经系统经常受到影响。除了机会性中枢神经系统感染和脑淋巴瘤,大约。20%的患者会出现与艾滋病毒相关的脑病。观察到两种主要的组织病理学表现。HIV脑白质病(进行性弥漫性脑白质病)的特征是大脑和小脑半球深部髓磷脂弥漫性丧失,伴有分散的多核巨细胞和小胶质细胞,但很少或没有炎症反应。HIV脑炎(多核巨细胞脑炎)与多核巨细胞积聚、炎症反应和局灶性坏死有关。在一些患者中,这两种模式可能重叠。为了鉴定中枢神经系统中的HIV基因组,使用聚合酶链反应(PCR)和编码gag基因109碱基对片段的引物分析了27例患者脑组织中HIV gag序列的存在。5例有临床和组织病理学证据为HIV脑病的患者中,HIV gag扩增均成功,但20例有机会性细菌、寄生虫和/或病毒感染或脑淋巴瘤的艾滋病患者中,HIV gag扩增呈阴性。这些结果强烈提示,组织病理学上可识别的HIV-脑病的演变与HIV的存在和/或组织浓度密切相关。由于在没有HIV相关组织病变的情况下没有HIV DNA扩增的病例,我们得出结论,HIV在中枢神经系统中的藏匿和复制迅速导致HIV相关脑病的相应临床和形态学变化。在两名患有严重HIV脑脊髓炎的儿童中,通过原位杂交在脑和脊髓的受累区域检测到大量HIV gag和env转录本。(摘要删节250字)
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