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首页> 外文期刊>African Journal of Laboratory Medicine >HIV and Tuberculosis co-infection impacts T-cell activation markers but not the numbers subset of regulatory T-cells in HIV-1 infected patients
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HIV and Tuberculosis co-infection impacts T-cell activation markers but not the numbers subset of regulatory T-cells in HIV-1 infected patients

机译:HIV和结核病合并感染影响HIV-1感染患者的T细胞活化标志物,但不影响调节性T细胞的数目子集

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Background: Tuberculosis (TB) has been shown to accelerate the clinical course of HIV infection, but the mechanisms by which this occurs are not well understood. Regulatory T-cells (Tregs)are known to dampen hyperactivation of the immune cells, but it remains unclear whether hyperactivation of T-cells in HIV infection is associated with a decrease of Tregs and what the effect Mycobacterium tuberculosis (MTB) co-infection has on T-cell activation and Tregs.Objectives: In this study, we aim to evaluate whether active TB is associated with the increased expression of T-cell activation markers and reduced number of Treg cells in HIV-1-infected patients.Methods: This study was conducted on 69 subjects consisting of 20 HIV-infected patients,20 HIV and MTB co-infected patients, 19 MTB-infected patients and 10 uninfected control subjects negative for both MTB and HIV. The frequencies of T-cell activation markers (CD38 and HLA-DR) and Treg cells (CD4+CD25+CD127-) were measured by flow cytometry.Results: Significantly higher expression of CD38 and HLA-DR on CD4+ and CD8+ T-cells was found in MTB and HIV co-infected patients compared with HIV-infected patients. However,no significant difference in the percentage of Treg cells was reported between HIV patients with TB and those without. The study also showed a negative correlation between regulatoryT-cells frequency and CD4+ T-cell counts.Conclusion: These results suggest that TB enhances the expression of peripheral T-cell activation markers during HIV infection, whilst having no impact on the percentages of Tregcells.
机译:背景:结核病(TB)已被证明可加速HIV感染的临床进程,但对其发生的机理尚不甚了解。调节性T细胞(Tregs)可以抑制免疫细胞的过度活化,但是尚不清楚HIV感染中T细胞的过度活化是否与Treg的减少有关,以及结核分枝杆菌(MTB)共感染的作用如何。目的:在这项研究中,我们旨在评估在感染HIV-1的患者中,活动性结核病是否与T细胞活化标志物的表达增加和Treg细胞数目减少有关。这项研究针对69名受试者,包括20名HIV感染患者,20名HIV和MTB合并感染患者,19名MTB感染患者和10名未感染MTB和HIV的对照受试者。流式细胞仪检测T细胞活化标志物(CD38和HLA-DR)和Treg细胞(CD4 + CD25 + CD127-)的频率。结果:CD38和HLA-DR在CD4 +和CD8 + T细胞上的表达明显更高与感染HIV的患者相比,在MTB和HIV合并感染的患者中发现HBsAg升高。然而,在患有结核病的HIV患者和没有结核病的HIV患者之间,Treg细胞百分比没有显着差异。该研究还显示调节性T细胞频率与CD4 + T细胞计数之间呈负相关。结论:这些结果表明,TB增强了HIV感染过程中外周T细胞活化标志物的表达,而对Tregcell的百分比没有影响。

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