Department of Dermatology, Division of Immunology, Center of Physiology, Pathophysiology and Immunology, Medical University Vienna, Vienna, Austria.
J Acquir Immune Defic Syndr. 2011 Feb 1;56(2):118-24. doi: 10.1097/QAI.0b013e3181fbab9f.
PD-1 expression on T cells correlates with T-cell exhaustion and disease progression in HIV-infected patients. Previous studies have shown that combinational antiretroviral therapy induced viral suppression results in immune restoration and reduced PD-1 expression. However, a significant number of patients fail to restore CD4 T cells despite suppression of HIV replication below limit of quantification. In this study, we have analyzed PD-1 expression on CD4 and CD8 T cells in patients with poor immune reconstitution despite successful highly active antiretroviral therapy. We found that T cells of such patients express significantly higher levels of PD-1 than patients who had normal recovery of CD4 cells after treatment. In contrast, failing immune reconstitution was not associated with the expression of activation markers, indicating that PD-1 is a unique marker for failing immune reconstitution despite viral suppression. Furthermore, we show that T cells from patients with poor immune recovery differ from T cells of elderly in respect of their marker profile. PD-1 expression negatively correlated with individual CD4 cell counts, and PD-1 expressing T cells were more prone to programmed death ligand-mediated inhibition of T-cell proliferation, indicating that PD-1-mediated T-cell suppression may have a role in impaired immune reconstitution in HIV patients.
PD-1 在 T 细胞上的表达与 HIV 感染患者的 T 细胞耗竭和疾病进展相关。先前的研究表明,联合抗逆转录病毒疗法诱导病毒抑制导致免疫恢复和 PD-1 表达减少。然而,尽管 HIV 复制被抑制到低于定量下限,但仍有相当数量的患者无法恢复 CD4 T 细胞。在这项研究中,我们分析了在接受高效抗逆转录病毒治疗后 CD4 细胞恢复正常的患者中,尽管免疫重建不良但 PD-1 在 CD4 和 CD8 T 细胞上的表达。我们发现,这些患者的 T 细胞表达的 PD-1 水平明显高于治疗后 CD4 细胞恢复正常的患者。相比之下,免疫重建失败与激活标志物的表达无关,这表明 PD-1 是尽管病毒抑制但免疫重建失败的独特标志物。此外,我们表明,尽管免疫恢复不良的患者的 T 细胞与老年患者的 T 细胞在标记物特征方面存在差异。PD-1 表达与个体 CD4 细胞计数呈负相关,并且表达 PD-1 的 T 细胞更容易受到程序性死亡配体介导的 T 细胞增殖抑制,这表明 PD-1 介导的 T 细胞抑制可能在 HIV 患者免疫重建受损中起作用。