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在开始抗逆转录病毒治疗(cART)之前,CD4恢复水平较低的HIV感染者体内就已经存在较高水平的白细胞介素-6(IL-6)、CD4周转率和调节性T细胞(Treg)频率。

Higher levels of IL-6, CD4 turnover and Treg frequency are already present before cART in HIV-infected subjects with later low CD4 recovery.

作者信息

Rosado-Sánchez Isaac, Jarrín Inmaculada, Pozo-Balado María M, de Pablo-Bernal Rebeca S, Herrero-Fernández Inés, Alvarez-Ríos Ana I, Rodríguez-Gallego Esther, Genebat Miguel, Vera Mar, Berenguer Juan, Martín María L, Bernal Enrique, Vidal Francesc, Blanco Julià, Leal Manuel, Pacheco Yolanda M

机构信息

Laboratory of Immunovirology, Institute of Biomedicine of Seville, IBiS, Virgen del Rocío University Hospital/CSIC/University of Seville, Seville 41013, Spain.

Institute of Health Carlos III, Madrid, Spain.

出版信息

Antiviral Res. 2017 Jun;142:76-82. doi: 10.1016/j.antiviral.2017.03.015. Epub 2017 Mar 24.

Abstract

Immunological characterization of HIV-infected subjects with low CD4-recovery (LR-subjects) has been extensively performed after a variable period of combined antiretroviral therapy (cART). We now explore immunological alterations present before the cART onset. In a case-control study, we selected pre-cART samples of HIV-subjects with and without low CD4-recovery after cART (n = 21 per group). CD4 T-cell activation, senescence and exhaustion related markers were not found specifically altered before cART initiation. On the other hand, we found that LR-subjects before cART already showed increased levels of IL6 (p = 0.009) and increased frequencies of Ki67+CD4 T-cells (p = 0.026), CD45RA-CD27+CD4 T-cells (p = 0.008) and Treg (p = 0.001), as well as increased expression of CD95 and CD127 on CD4 T-cells (p = 0.016; p = 0.032, respectively). These parameters characterize the immunological damage in LR-subjects before the cART onset and could be associated to the mechanisms hindering the subsequent CD4 recovery.

摘要

在接受不同疗程的联合抗逆转录病毒疗法(cART)后,已对CD4恢复率低的HIV感染者(LR受试者)进行了广泛的免疫学特征分析。我们现在探究cART开始前存在的免疫学改变。在一项病例对照研究中,我们选取了cART后有和没有低CD4恢复率的HIV感染者的cART前样本(每组n = 21)。在开始cART前,未发现CD4 T细胞活化、衰老和耗竭相关标志物有特异性改变。另一方面,我们发现cART前的LR受试者已经表现出IL6水平升高(p = 0.009),Ki67 + CD4 T细胞(p = 0.026)、CD45RA - CD27 + CD4 T细胞(p = 0.008)和调节性T细胞(Treg)频率增加(p = 0.001),以及CD4 T细胞上CD95和CD127的表达增加(分别为p = 0.016;p = 0.032)。这些参数表征了cART开始前LR受试者中的免疫损伤,并且可能与阻碍随后CD4恢复的机制有关。

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