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首页> 外文期刊>The New Microbiologica >Interferon-y release assay in HIV-infected patients with active tuberculosis: impact of antituberculous drugs on host immune response
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Interferon-y release assay in HIV-infected patients with active tuberculosis: impact of antituberculous drugs on host immune response

机译:HIV感染的活动性肺结核患者的干扰素γ释放测定:抗结核药物对宿主免疫反应的影响

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The objective of the study was to:1) investigate the performance of QuantiFERON-TB Gold In-Tube (QFT-GIT) in HIV-infected patients with active tuberculosis (TB);2) evaluate the sequential changes in QFT-GIT assay during the treatment response;3) investigate the direct in vitro effects of antituberculous drugs on both secretion of IFN-y and apoptosis of T cells. Forty-four HIV-patients with active TB were enrolled and tested with QFT-GIT.Thirteen of them were followed longitudinally by QFT-GIT, performed at baseline and six and nine months after TB-treatment onset. For in vitro experiments, cells from healthy donors and HIV-naive subjects were pretreated with four antituberculous-drugs, and then examined for IFN-y secretion and apoptosis of T-cells. The QFT-GIT was positive in 66%, negative in 11.3% and indeterminate in 22.7%. Longitudinal analysis in 13 HIV-TB subjects showed that at therapy completion a reversion to negative response was found only in 38.4% of patients, but in 30.7% the QFT-GIT remained positive. Overall, during the anti-TB treatment no significant decrease in average IFN-y response was observed in these patients (p<0.001). In vitro experiments showed that the four antituberculous-drugs, within the range of therapeutically achievable concentrations, did not exert any down-regulatory effect on IFN-y production and did not have any effect on apoptosis of T cells from HIV naive subjects. Despite the high rate of indeterminate results, QFT-GIT assay may represent a good toolin the diagnostic workup for active TB in HIV-patients. Although the antituberculous drugs do not have any direct effect on host immune response to mycobacterial antigen, changes in longitudinal IGRA response have been found during in vivo anti-TB treatment.
机译:该研究的目的是:1)研究QuantiFERON-TB黄金管(QFT-GIT)在HIV感染的活动性肺结核(TB)患者中的表现; 2)评价QFT-GIT测定在治疗过程中的顺序变化3)研究抗结核药物对IFN-γ分泌和T细胞凋亡的直接体外作用。纳入了44例活动性结核病的HIV患者,并进行了QFT-GIT测试。其中13名患者进行了QFT-GIT纵向研究,分别在基线以及结核病治疗开始后的六个月和九个月进行。对于体外实验,将健康供体和未感染HIV的受试者的细胞用四种抗结核药物进行预处理,然后检查IFN-γ分泌和T细胞凋亡。 QFT-GIT的阳性率为66%,阴性的为11.3%,不确定的为22.7%。对13名HIV-TB受试者进行的纵向分析显示,在治疗完成后,仅38.4%的患者恢复了阴性反应,但在30.7%的患者中QFT-GIT仍保持阳性。总体而言,在抗结核治疗期间,这些患者的平均IFN-γ反应无明显下降(p <0.001)。体外实验表明,在治疗上可达到的浓度范围内,这四种抗结核药物对IFN-γ的产生没有任何下调作用,对未接触HIV的受试者的T细胞凋亡也没有任何作用。尽管不确定结果的发生率很高,但是QFT-GIT分析可能代表了对艾滋病毒患者活动性结核病进行诊断性检查的良好方法。尽管抗结核药对宿主对分枝杆菌抗原的免疫反应没有任何直接影响,但在体内抗结核治疗期间发现了纵向IGRA反应的变化。

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