Department of Infectious Diseases, The University of Melbourne at The Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia.
Department of Infectious Diseases, Alfred Hospital and Monash University and the Alfred Hospital, Melbourne, VIC, Australia.
Front Immunol. 2023 Mar 28;14:1123342. doi: 10.3389/fimmu.2023.1123342. eCollection 2023.
In people with HIV (PWH) both off and on antiretroviral therapy (ART), the expression of immune checkpoint (IC) proteins is elevated on the surface of total and HIV-specific T-cells, indicating T-cell exhaustion. Soluble IC proteins and their ligands can also be detected in plasma, but have not been systematically examined in PWH. Since T-cell exhaustion is associated with HIV persistence on ART, we aimed to determine if soluble IC proteins and their ligands also correlated with the size of the HIV reservoir and HIV-specific T-cell function.
We used multiplex bead-based immunoassay to quantify soluble programmed cell death protein 1 (PD-1), cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), lymphocyte activation gene-3 (LAG-3), T cell immunoglobulin domain and mucin domain 3 (TIM-3), PD-1 Ligand 1 (PD-L1) and PD-1 Ligand 2 (PD-L2) in plasma from PWH off ART (n=20), on suppressive ART (n=75) and uninfected controls (n=20). We also quantified expression of membrane-bound IC and frequencies of functional T-cells to Gag and Nef peptide stimulation on CD4+ and CD8+ T-cells using flow cytometry. The HIV reservoir was quantified in circulating CD4+ T-cells using qPCR for total and integrated HIV DNA, cell-associated unspliced HIV RNA and 2LTR circles.
Soluble (s) PD-L2 level was higher in PWH off and on ART compared to uninfected controls. Higher levels of sPD-L2 correlated with lower levels of HIV total DNA and higher frequencies of gag-specific CD8+ T-cells expressing CD107a, IFNγ or TNFα. In contrast, the concentration of sLAG-3 was similar in uninfected individuals and PWH on ART, but was significantly elevated in PWH off ART. Higher levels of sLAG-3 correlated with higher levels of HIV total and integrated DNA, and lower frequency of gag-specific CD4+ T cells expressing CD107a. Similar to sLAG-3, levels of sPD-1 were elevated in PWH off ART and normalized in PWH on ART. sPD-1 was positively correlated with the frequency of gag-specific CD4+ T cells expressing TNF-a and the expression of membrane-bound PD-1 on total CD8+ T-cells in PWH on ART.
Plasma soluble IC proteins and their ligands correlate with markers of the HIV reservoir and HIV-specific T-cell function and should be investigated further in in large population-based studies of the HIV reservoir or cure interventions in PWH on ART.
在接受抗逆转录病毒治疗(ART)的 HIV 感染者(PWH)中,总 T 细胞和 HIV 特异性 T 细胞表面的免疫检查点(IC)蛋白表达升高,表明 T 细胞耗竭。可溶性 IC 蛋白及其配体也可在血浆中检测到,但尚未在 PWH 中进行系统研究。由于 T 细胞耗竭与 ART 治疗下的 HIV 持续存在有关,我们旨在确定可溶性 IC 蛋白及其配体是否也与 HIV 储存库的大小和 HIV 特异性 T 细胞功能相关。
我们使用基于多重珠的免疫测定法,定量检测了接受 ART 治疗的 HIV 感染者(n=20)、接受抑制性 ART 治疗的 HIV 感染者(n=75)和未感染对照者(n=20)的血浆中可溶性程序性死亡蛋白 1(PD-1)、细胞毒性 T 淋巴细胞相关蛋白 4(CTLA-4)、淋巴细胞激活基因 3(LAG-3)、T 细胞免疫球蛋白和粘蛋白结构域 3(TIM-3)、PD-1 配体 1(PD-L1)和 PD-1 配体 2(PD-L2)。我们还使用流式细胞术,通过对 Gag 和 Nef 肽刺激的 CD4+和 CD8+T 细胞进行膜结合 IC 表达和功能 T 细胞频率的定量,来检测 HIV 储存库。通过 qPCR 检测循环 CD4+T 细胞中的总 HIV DNA、整合 HIV DNA、细胞相关未剪接 HIV RNA 和 2LTR 环,对 HIV 储存库进行定量。
与未感染对照者相比,接受 ART 治疗的 PWH 和未接受 ART 治疗的 PWH 的可溶性(s)PD-L2 水平均升高。较高的 sPD-L2 水平与较低的总 HIV DNA 水平和较高的 gag 特异性 CD8+T 细胞表达 CD107a、IFNγ或 TNFα的频率相关。相比之下,未感染个体和接受 ART 治疗的 HIV 感染者的 sLAG-3 浓度相似,但未接受 ART 治疗的 HIV 感染者的 sLAG-3 浓度显著升高。较高的 sLAG-3 水平与较高的总 HIV DNA 和整合 HIV DNA 水平以及 gag 特异性 CD4+T 细胞表达 CD107a 的频率较低相关。与 sLAG-3 相似,sPD-1 在未接受 ART 治疗的 PWH 中升高,并在接受 ART 治疗的 PWH 中恢复正常。sPD-1 与接受 ART 治疗的 PWH 中 gag 特异性 CD4+T 细胞表达 TNF-α的频率和总 CD8+T 细胞上膜结合 PD-1 的表达呈正相关。
血浆可溶性 IC 蛋白及其配体与 HIV 储存库和 HIV 特异性 T 细胞功能的标志物相关,应在接受 ART 治疗的 HIV 感染者的 HIV 储存库或治愈干预的大型基于人群的研究中进一步研究。