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艾滋病痴呆综合征:病理学、发病机制及未来方向。

AIDS-dementia-complex: pathology, pathogenesis and future directions.

作者信息

Dal Canto M C

机构信息

Division of Neuropathology, Northwestern University Medical School, Chicago, Illinois.

出版信息

Ital J Neurol Sci. 1989 Jun;10(3):277-87. doi: 10.1007/BF02333773.

Abstract

Acquired immunodeficiency syndrome (AIDS), first described in 1981, is produced by infection with a retrovirus of the lentivirus family, now called human immunodeficiency virus (HIV). While, initially, the disease was almost exclusively seen in homosexual men, it has become apparent that numerous other categories of people are at risk, i.e., drug addicts who share dirty needles, hemophiliacs and haitians. In addition, epidemiological data from the industrialized nations clearly indicate that heterosexual contact is becoming an important source of viral transmission, as it has been known to occur in several african nations for many years. Initially, studies on patients with AIDS mainly focused on the immunosuppressive effects of the virus and on the various opportunistic infections and neoplastic complications that followed. Not much attention was given to a possible direct HIV infection of the nervous system. Consequently, patients who presented with neurological findings were simply considered to harbor in the CNS the same complications that occurred in other organs. While this was true in many cases, it has become also apparent that important changes in the central and peripheral nervous systems are due to direct viral involvement of these tissues. The first important step in the understanding of nervous system involvement in AIDS was the demonstration, in 1985, of HIV in the CSF and cerebral tissues of patients with neurological symptoms (47). Further studies have shown that, while opportunistic infections and neoplastic complications certainly contribute to the neurological morbidity of AIDS, the most important neuropathological changes, particularly in the brain, are due to direct HIV infection. The aim of this paper is to review the pathology of HIV-induced encephalitis and to discuss pathogenetic hypotheses regarding mechanisms of HIV-mediated tissue injury and the clinical manifestations that follow, particularly the syndrome now known as AIDS-Dementia-Complex (ADC). First, however, it may be appropriate to quickly review some basic notions on the biology of the virus.

摘要

获得性免疫缺陷综合征(艾滋病)于1981年首次被描述,它是由感染慢病毒科的一种逆转录病毒引起的,这种病毒现在被称为人类免疫缺陷病毒(HIV)。最初,这种疾病几乎只在同性恋男性中出现,但现在很明显,其他许多类别的人也有感染风险,即共用不洁针头的吸毒者、血友病患者和海地人。此外,工业化国家的流行病学数据清楚地表明,异性接触正成为病毒传播的一个重要来源,因为在几个非洲国家,异性接触传播病毒的情况已经存在多年。最初,对艾滋病患者的研究主要集中在病毒的免疫抑制作用以及随之而来的各种机会性感染和肿瘤并发症上。人们对HIV可能直接感染神经系统的情况关注不多。因此,出现神经系统症状的患者仅仅被认为是在中枢神经系统中存在与其他器官相同的并发症。虽然在许多情况下确实如此,但现在也很明显,中枢和周围神经系统的重要变化是由于这些组织直接受到病毒感染。1985年,在有神经症状的患者的脑脊液和脑组织中发现了HIV,这是理解艾滋病中神经系统受累的第一个重要步骤(47)。进一步的研究表明,虽然机会性感染和肿瘤并发症肯定会导致艾滋病的神经病变,但最重要的神经病理变化,特别是在大脑中,是由于HIV的直接感染。本文的目的是回顾HIV诱导的脑炎的病理学,并讨论关于HIV介导的组织损伤机制以及随之而来的临床表现,特别是现在被称为艾滋病痴呆综合征(ADC)的发病机制假说。然而,首先快速回顾一下关于该病毒生物学的一些基本概念可能是合适的。

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