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脑脊液中人类免疫缺陷病毒1型的病毒学标志物。艾滋病神经行为研究中心小组。

Virologic markers of human immunodeficiency virus type 1 in cerebrospinal fluid. The HIV Neurobehavioral Research Center Group.

作者信息

Spector S A, Hsia K, Pratt D, Lathey J, McCutchan J A, Alcaraz J E, Atkinson J H, Gulevich S, Wallace M, Grant I

机构信息

Department of Pediatrics, University of California, San Diego, La Jolla 92093.

出版信息

J Infect Dis. 1993 Jul;168(1):68-74. doi: 10.1093/infdis/168.1.68.

Abstract

As part of a longitudinal study, 265 cerebrospinal fluid (CSF) specimens from 204 human immunodeficiency virus type 1 (HIV-1)-seropositive subjects and 43 seronegative controls were evaluated. Of the 204 seropositive persons, 78 (38%) had > or = 1 CSF culture positive for HIV-1; the probability of being culture positive increased as the number of CSF samples obtained increased (P = .0018). Significantly correlated with culture positivity were elevations in CSF protein level (P = .014) and CSF white blood cell count (P = .001). Virus was more readily cultured from clarified CSF (89%, 42/47) than from the cellular fraction (30%, 14/47; P < .00001). Amplification of HIV-1 DNA by polymerase chain reaction (PCR) from 25 seropositive persons was positive in 9 (82%) of 11 culture-positive and in 4 (29%) of 14 culture-negative specimens, while amplification of viral RNA detected all 11 culture-positive and 9 (64%) of the 14 culture-negative CSF specimens. These data support the hypothesis that the development of HIV-1-associated neurocognitive disorders are not dependent solely on the presence of HIV-1 within the central nervous system.

摘要

作为一项纵向研究的一部分,对来自204名1型人类免疫缺陷病毒(HIV-1)血清反应阳性受试者和43名血清反应阴性对照的265份脑脊液(CSF)标本进行了评估。在204名血清反应阳性者中,78人(38%)的CSF培养有≥1次HIV-1阳性;随着获取的CSF样本数量增加,培养呈阳性的概率也增加(P = 0.0018)。与培养阳性显著相关的是CSF蛋白水平升高(P = 0.014)和CSF白细胞计数升高(P = 0.001)。从澄清的CSF中培养病毒比从细胞成分中更容易(89%,42/47),而从细胞成分中培养的阳性率为30%(14/47;P < 0.00001)。通过聚合酶链反应(PCR)对25名血清反应阳性者的HIV-1 DNA进行扩增,在11份培养阳性标本中有9份(82%)呈阳性,在14份培养阴性标本中有4份(29%)呈阳性,而病毒RNA扩增检测到所有11份培养阳性的CSF标本以及14份培养阴性标本中的9份(64%)。这些数据支持这样的假设,即HIV-1相关神经认知障碍的发生并非仅取决于中枢神经系统内HIV-1的存在。

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