CD14+ cd16低单核细胞亚群预测非进展性HIV疾病:一种新的预后和诊断生物标志物的证据

K. Matlho, X. Wang, Viviane Conceição, Suneth S. Perera, Bin Wang, Maly Soedjono, Ma Jin Min, N. Saksena
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引用次数: 1

摘要

单核细胞具有表型柔韧性,这使得它们在对抗HIV感染中发挥了几个重要的免疫作用。根据CD14和CD16抗原的表达,单核细胞可以被细分为亚群。虽然CD4+ T细胞计数已被证明可以预测HIV病毒血症,但这些单核细胞亚群在血浆病毒血症不同阶段的实际预测价值尚不清楚。我们从可检测到和低于可检测到的血浆病毒血症的HIV+患者、HIV+长期非进展者(LTNP)和HIV阴性个体中获得离体单核细胞。我们将单核细胞细分为CD14+/ CD16-低、中、高人群,并观察了不同阶段HIV+患者中CD14和CD16抗原表达的表型变化。使用FACSCanto(6色)流式细胞仪,从50例HIV+个体(14例病毒血症和29例低于可检测水平(BDL),同时进行HAART治疗,7例治疗naïve,病毒血症LTNP)和6例HIV阴性供者的EDTA血液中检测单核细胞表面标志物(CD14+/CD16)的表达。用FACSDiva (v6.1.2)软件在FACSCantoA上测量CD16/CD14+亚群的百分比,用FlowJo软件(v10.0.7)分析。通过单核细胞群CD14+、CD16高、中、低的分类,我们可以清楚地区分病毒血症和病毒血症HIV患者。在hiv阴性个体和LTNPS中,cd16低人群(80%)显著升高(57%),而在haart治疗组中,这一比例为9%。值得注意的是,在HAART治疗期间,尽管完全控制了病毒,但cd16低的人群未能恢复,这表明它们作为病毒控制指标的决定性作用,在ltnp中显著突出。相比之下,haart治疗组显示cd16高人群升高(34%),而病毒血症组的百分比相对较低(3%)。在HIV阴性和未进展的HIV+个体中,cd16 -低人群的稳定维持和升高以及cd16 -高人群的显著低水平与ltnp中HIV的自然控制相关。低cd16单核细胞群体的这一特征可以作为预测血浆病毒血症和免疫系统强度的生物标志物。2576 - 9588 . DOI: 10.29011 /。100028
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CD14+CD16-Low Monocyte Subset Predicts Non-Progressive HIV Disease: Evidence of A New Prognostic and Diagnostic Biomarker
Monocytes are phenotypically pliable, which allows them to play several significant immunological roles in combating HIV infection. Monocytes can be subcategorized into subsets based on the expression of CD14 and CD16 antigens. Although the CD4+ T cell counts have been shown to predict HIV viremia, the actual predictive value of these monocyte subsets at different stages of plasma viremia is not known. We derived ex-vivo monocytes from HIV+ patients with detectable and below detectable plasma viremia, HIV+ Long-Term Non-Progressors (LTNP) and HIV negative individuals. We subdivided monocytes into CD14+/ CD16-low, medium and high populations and visualized the phenotypic changes in expression of both CD14 and CD16 antigens in HIV+ patients at different stages of HIV disease. The expression of surface markers on monocytes (CD14+/CD16) was measured from the EDTA blood of 50 HIV+ individuals [14 viremic and 29 Below Detectable Level (BDL) whilst on HAART, 7 therapy naïve, aviremic LTNP’s] and 6 HIVnegative donors using the FACSCanto (6-color) flow cytometer. Percentage of CD16/CD14+ sub-populations were measured on FACSCantoA with FACSDiva (v 6.1.2) software and analysed by FlowJo software (v10.0.7), respectively. By categorizing monocyte population into CD14+, CD16 high, medium and low, we could clearly discriminate between viremic and aviremic HIV patients. There was considerable elevation of CD16-low population (80%) in HIV-negative individuals and LTNPS (57%), as opposed to 9% in HAART-treated group. Noteworthy was the CD16-low population failed to recover despite complete viral control during HAART therapy suggesting their definitive role as indicators of viremic control as seen with their marked prominence in LTNPs. In contrast, the HAART-treated group showed elevated CD16-high populations (34%), as opposed to relatively low percentages in the viremic group (3%). The robust maintenance and elevation of CD16-low populations and substantial low levels of CD16-high populations distinctively in HIV-negative and non-progressing HIV+ individuals correlated with the natural control of HIV in LTNPs. This feature of CD16-low monocytic population can be exploited as a biomarker in predicting plasma viremia and the strength of the immune system. DOI: 10.29011/2576-9588. 100028
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