Mbow Moustapha, Santos Ndèye S S, Camara Makhtar, Ba Awa, Niang Aliou, Daneau Géraldine, Wade Djibril, Diallo Abdou A, Toupane Maxim, Diakhaté Maïmouna, Lèye Nafissatou, Diaw Papa A, Mboup Souleymane, Kestens Luc, Dieye Tandakha N
Laboratory of Bacteriology and Virology, Aristide Le Dantec University Hospital, Dakar, Sénégal.
Institute of Tropical Medicine, Unit of Immunology, Department of Biomedical Sciences, Antwerp, Belgium.
Afr J Lab Med. 2013 Sep 2;2(1):76. doi: 10.4102/ajlm.v2i1.76. eCollection 2013.
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 (MTB) co-infection has on T-cell activation and Tregs.
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.
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 (CD4CD25CD127-) were measured by flow cytometry.
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 regulatory T-cells frequency and CD4 T-cell counts.
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 Treg cells.
结核病已被证明会加速HIV感染的临床进程,但其发生机制尚不清楚。已知调节性T细胞(Tregs)可抑制免疫细胞的过度激活,但HIV感染中T细胞的过度激活是否与Tregs数量减少有关,以及结核分枝杆菌(MTB)合并感染对T细胞激活和Tregs有何影响仍不清楚。
在本研究中,我们旨在评估活动性结核病是否与HIV-1感染患者T细胞激活标志物表达增加和调节性T细胞数量减少有关。
本研究对69名受试者进行,包括20名HIV感染患者、20名HIV和MTB合并感染患者、19名MTB感染患者以及10名MTB和HIV均为阴性的未感染对照受试者。通过流式细胞术检测T细胞激活标志物(CD38和HLA-DR)和调节性T细胞(CD4CD25CD127-)的频率。
与HIV感染患者相比,MTB和HIV合并感染患者的CD4和CD8 T细胞上CD38和HLA-DR的表达明显更高。然而,有结核病的HIV患者和无结核病的HIV患者之间调节性T细胞百分比没有显著差异。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。
这些结果表明,结核病在HIV感染期间会增强外周T细胞激活标志物的表达,而对调节性T细胞百分比没有影响。