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HIV阳性个体单核细胞中细胞因子表达失调。

Dysregulation of cytokine expression in monocytes from HIV-positive individuals.

作者信息

Lathey J L, Kanangat S, Rouse B T, Agosti J M, Spector S A

机构信息

Department of Pediatrics, University of California, San Diego, La Jolla 92093-0672.

出版信息

J Leukoc Biol. 1994 Sep;56(3):347-52. doi: 10.1002/jlb.56.3.347.

Abstract

Because HIV may alter the production of inflammatory factors produced by monocytes, the expression of tumor necrosis factor alpha (TNF-alpha), tissue factor (TF), interleukin (IL)-1 beta, and IL-6 was evaluated in 47 HIV-seropositive persons and seronegative control subjects. RNA was extracted from freshly isolated lipopolysaccharide (LPS)-stimulated or unstimulated monocytes. Cytokine and TF expression was quantitated by dot blot hybridization or a reverse transcription polymerase chain reaction (RT-PCR). A significant depression of TF mRNA was observed in LPS-stimulated monocytes (66% less in AIDS, 20% less in AIDS-related complex (ARC), and 0% less in asymptomatic patients), whereas normal responses were observed for TNF-alpha, IL-1 beta, and IL-6. When constitutive expression was measured in unstimulated monocytes by RT-PCR, a differential pattern was also observed. TNF-alpha and IL-1 beta were positive in 85% of asymptomatic persons, compared with only 27% of ARC and 42% of AIDS patients. Expression of IL-6 was observed in lower proportions, 27-30%, with no significant differences among disease states. All samples were negative for TF. Thus, the regulation of inflammatory molecules is differentially altered in individuals with HIV infection. TF is preferentially down-regulated, compared with TNF-alpha, IL-1 beta, and IL-6, in LPS-stimulated monocytes as patients progress to AIDS. TNF-alpha and IL-1 beta are preferentially up-regulated, compared with IL-6 and TF, in unstimulated monocytes in asymptomatic persons, with a loss of up-regulation as patients progress to AIDS.

摘要

由于HIV可能会改变单核细胞产生的炎症因子,因此在47名HIV血清阳性者和血清阴性对照者中评估了肿瘤坏死因子α(TNF-α)、组织因子(TF)、白细胞介素(IL)-1β和IL-6的表达。从新鲜分离的经脂多糖(LPS)刺激或未刺激的单核细胞中提取RNA。通过斑点杂交或逆转录聚合酶链反应(RT-PCR)对细胞因子和TF表达进行定量。在LPS刺激的单核细胞中观察到TF mRNA显著降低(艾滋病患者降低66%,艾滋病相关综合征(ARC)患者降低20%,无症状患者降低0%),而TNF-α、IL-1β和IL-6的反应正常。当通过RT-PCR在未刺激的单核细胞中测量组成型表达时,也观察到了差异模式。TNF-α和IL-1β在85%的无症状者中呈阳性,而ARC患者中只有27%,艾滋病患者中只有42%。IL-6的表达比例较低,为27%-30%,疾病状态之间无显著差异。所有样本的TF均为阴性。因此,HIV感染个体中炎症分子的调节存在差异改变。随着患者进展为艾滋病,在LPS刺激的单核细胞中,与TNF-α、IL-1β和IL-6相比,TF优先下调。在无症状者未刺激的单核细胞中,与IL-6和TF相比,TNF-α和IL-1β优先上调,随着患者进展为艾滋病,上调作用丧失。

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