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在无艾滋病相关继发感染情况下晚期HIV感染中的肿瘤坏死因子-α

Tumor necrosis factor-alpha in advanced HIV infection in the absence of AIDS-related secondary infections.

作者信息

Jones P D, Shelley L, Wakefield D

机构信息

Department of Infectious Diseases, Prince Henry Hospital, Little Bay, Australia.

出版信息

J Acquir Immune Defic Syndr (1988). 1992 Dec;5(12):1266-71.

PMID:1453335
Abstract

The effect of HIV infection on the production of tumor necrosis factor-alpha (TNF-alpha) was examined in patients with advanced human immunodeficiency virus (HIV) infection in the absence of AIDS-related secondary infections. Serum TNF-alpha and TNF-alpha production in vitro were measured by enzyme-linked immunosorbent assay in 26 male homosexuals with CDC stage IV HIV infection without active AIDS-related secondary infections. In vitro TNF-alpha production was assayed from cultured peripheral blood mononuclear cells (PBMs) or whole blood cultures under conditions for minimising endotoxin contamination. PBMs and whole blood were cultured with and without lipopolysaccharide (LPS). Results were compared with those for 13 HIV-seronegative age- and sex-matched controls. Serum TNF-alpha concentrations were 5 +/- 16 pg/ml in HIV-infected patients and 12 +/- 17 pg/ml in controls. TNF-alpha levels in unstimulated cultures of PBMs obtained from patients were 426 +/- 511 pg/ml and 456 +/- 428 pg/ml in control cultures. There was no difference between groups in the maximal responses of cultured PBMs to stimulation with LPS (2,229 +/- 1,593 pg/ml vs. 2,504 +/- 961 pg/ml). TNF-alpha levels from unstimulated and LPS-stimulated whole blood cultures were not significantly different after adjusting for the number of cultured monocytes (2,038 +/- 1,469 pg/ml vs. 1,511 +/- 488 pg/ml). In 10 patients (38%) the TNF-alpha levels from stimulated whole blood cultures were greater than the 95% confidence interval of the control group. TNF-alpha levels in patients were not significantly altered by antiretroviral therapy.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在没有艾滋病相关继发感染的晚期人类免疫缺陷病毒(HIV)感染患者中,研究了HIV感染对肿瘤坏死因子-α(TNF-α)产生的影响。通过酶联免疫吸附测定法,对26名处于疾病控制中心IV期HIV感染且无活动性艾滋病相关继发感染的男性同性恋者,测定其血清TNF-α和体外TNF-α的产生。在尽量减少内毒素污染的条件下,从培养的外周血单个核细胞(PBMs)或全血培养物中检测体外TNF-α的产生。PBMs和全血分别在有和没有脂多糖(LPS)的情况下进行培养。将结果与13名年龄和性别匹配的HIV血清阴性对照者的结果进行比较。HIV感染患者的血清TNF-α浓度为5±16 pg/ml,对照组为12±17 pg/ml。患者来源的PBMs未刺激培养物中的TNF-α水平为426±511 pg/ml,对照培养物中为456±428 pg/ml。培养的PBMs对LPS刺激的最大反应在两组之间没有差异(2229±1593 pg/ml对2504±961 pg/ml)。在调整培养的单核细胞数量后,未刺激和LPS刺激的全血培养物中的TNF-α水平没有显著差异(2038±1469 pg/ml对1511±488 pg/ml)。在10名患者(38%)中,刺激的全血培养物中的TNF-α水平高于对照组的95%置信区间。抗逆转录病毒疗法未显著改变患者的TNF-α水平。(摘要截断于250字)

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Clin Exp Immunol. 1993 Sep;93(3):350-5. doi: 10.1111/j.1365-2249.1993.tb08184.x.