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HIV 白质脑病与神经元中肿瘤坏死因子α的表达

HIV leucoencephalopathy and TNFalpha expression in neurones.

作者信息

Rostasy K, Monti L, Lipton S A, Hedreen J C, Gonzalez R G, Navia B A

机构信息

Paediatric Neurology, University of Göttingen, Germany.

出版信息

J Neurol Neurosurg Psychiatry. 2005 Jul;76(7):960-4. doi: 10.1136/jnnp.2004.036889.

Abstract

BACKGROUND

Human immunodeficiency virus (HIV) leucoencephalopathy (HIVL) is an uncommon and rapidly progressive form of AIDS dementia complex (ADC) that has remained poorly understood. Tumour necrosis factor alpha (TNFalpha), which has been implicated in the pathogenesis of ADC, is predominantly localised in macrophages in the HIV infected brain, although in vitro studies indicate that neurones can express this cytokine.

OBJECTIVE

To examine the clinical/neuroradiological features of HIVL and the expression of TNFalpha in HIVL.

METHODS

Six patients who presented with rapidly progressive dementia within four to 12 weeks of the primary manifestation of their HIV infection were evaluated. Clinical history, treatment regimens, and imaging studies were reviewed, and brain samples from three of the patients were studied by means of immunohistochemistry.

RESULTS

Imaging studies showed diffuse bilateral deep white matter changes in all six patients. Clinical and imaging abnormalities improved in five of the six patients within weeks after initiation of antiretroviral treatment. Brain biopsies of two showed pronounced microglia/macrophage activation, but only scant viral protein (gp41) expression. Staining for TNFalpha was found in microglia/macrophages, and surprisingly, in neurones also. Postmortem analysis of a third patient also showed TNFalpha expression in neurones of the frontal cortex and basal ganglia.

CONCLUSION

This study provides the first demonstration of staining for TNFalpha in the neurones of the HIV infected brain, and suggests that the process underlying this rapidly progressive form of ADC may reflect indirect mechanisms mediated by host factors, particularly TNFalpha.

摘要

背景

人类免疫缺陷病毒(HIV)白质脑病(HIVL)是获得性免疫缺陷综合征痴呆综合征(ADC)中一种罕见且进展迅速的形式,人们对其了解甚少。肿瘤坏死因子α(TNFα)与ADC的发病机制有关,主要定位于HIV感染大脑中的巨噬细胞,尽管体外研究表明神经元也能表达这种细胞因子。

目的

研究HIVL的临床/神经影像学特征以及TNFα在HIVL中的表达。

方法

对6例在HIV感染初发症状出现后4至12周内出现快速进展性痴呆的患者进行评估。回顾临床病史、治疗方案和影像学研究,并对其中3例患者的脑样本进行免疫组织化学研究。

结果

影像学研究显示所有6例患者均有双侧弥漫性深部白质改变。6例患者中有5例在开始抗逆转录病毒治疗后数周内临床和影像学异常得到改善。2例患者的脑活检显示小胶质细胞/巨噬细胞明显活化,但病毒蛋白(gp41)表达很少。在小胶质细胞/巨噬细胞中发现了TNFα染色,令人惊讶的是,在神经元中也有。对第3例患者的尸检分析也显示额叶皮质和基底节的神经元中有TNFα表达。

结论

本研究首次证实了HIV感染大脑的神经元中有TNFα染色,并表明这种快速进展形式的ADC的潜在过程可能反映了由宿主因素特别是TNFα介导的间接机制。

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