MicroRNA Expression Levels in Peripheral Blood Mononuclear Cells from Human Immunodeficiency Virus Type 1 Positive Individuals and Relationship with Different Levels of Viral Suppression.

IF 1.5 4区 医学 Q4 IMMUNOLOGY AIDS research and human retroviruses Pub Date : 2024-05-01 Epub Date: 2023-07-31 DOI:10.1089/aid.2022.0165
Daniele Di Carlo, Francesca Falasca, Laura Mazzuti, Giuliana Guerrizio, Giuseppe Migliara, Marta Santori, Alessandro Lazzaro, Ivano Mezzaroma, Gabriella D'Ettorre, Caterina Fimiani, Giancarlo Iaiani, Guido Antonelli, Ombretta Turriziani
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Abstract

The persistence of low human immunodeficiency virus type 1 (HIV-1) replication in individuals undergoing antiretroviral therapy (ART) still threatens their health. Previous findings have shown that microRNAs (miRNAs) could interfere with several steps of the viral life cycle. Herein, we set out to investigate the expression of miR-150, miR-223, miR-382, miR-324-5p, miR-33a-5p, miR-34a, and miR-132 in the whole peripheral blood mononuclear cell (PBMC) population from people living with HIV-1 showing different levels of viral suppression. Levels of PBMC-associated miRNAs were analyzed in 30 individuals with undetectable viremia (target not detected) and 30 individuals with detectable low-level viremia (1-200 copies/mL). In addition, 30 samples from treatment-naive (NAIVE) individuals were investigated. Results were compared to a control group of 28 HIV-negative donors. All miRNAs analyzed were strongly downregulated in the NAIVE population, either compared to the treated group or to controls. Stratification of ART-treated donors according to the therapeutic regimen showed the downregulation of miR-33a-5p in subjects treated with non-nucleoside reverse transcriptase inhibitors compared with those treated with protease inhibitors. Collectively, the present study shows that uncontrolled viral replication leads to profound miRNA deregulation while treated individuals, irrespective of the degree of viral suppression, and even the types of antiviral drugs seem to be specifically associated with miRNA expression profiles. These evidences suggest that virological suppression could be favored by miRNA modulation.

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人类免疫缺陷病毒 1 型阳性个体外周血单核细胞中的微 RNA 表达水平及其与不同病毒抑制水平的关系。
正在接受抗逆转录病毒疗法(ART)的人体内持续存在的低水平人类免疫缺陷病毒 1 型(HIV-1)复制仍然威胁着他们的健康。以前的研究结果表明,微RNA(miRNA)可以干扰病毒生命周期的几个步骤。在此,我们着手研究了不同病毒抑制水平的 HIV-1 感染者的整个外周血单核细胞(PBMC)中 miR-150、miR-223、miR-382、miR-324-5p、miR-33a-5p、miR-34a 和 miR-132 的表达情况。我们分析了 30 名检测不到病毒血症(未检测到目标)的患者和 30 名检测到低水平病毒血症(1-200 拷贝/毫升)的患者的 PBMC 相关 miRNA 水平。此外,还调查了 30 份未接受治疗者(NAIVE)的样本。研究结果与由 28 名 HIV 阴性捐献者组成的对照组进行了比较。与治疗组或对照组相比,所有被分析的 miRNA 在 NAIVE 群体中均强烈下调。根据治疗方案对接受抗逆转录病毒疗法治疗的供体进行分层,结果显示,与接受蛋白酶抑制剂治疗的受试者相比,接受非核苷类逆转录酶抑制剂治疗的受试者体内的 miR-33a-5p 出现了下调。总之,本研究表明,无论病毒抑制程度如何,病毒复制失控都会导致接受治疗者体内的 miRNA 出现严重的失调,甚至抗病毒药物的类型似乎也与 miRNA 的表达谱有特殊关系。这些证据表明,miRNA 的调节可能有利于病毒抑制。
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来源期刊
CiteScore
3.10
自引率
6.70%
发文量
201
审稿时长
3-6 weeks
期刊介绍: AIDS Research and Human Retroviruses was the very first AIDS publication in the field over 30 years ago, and today it is still the critical resource advancing research in retroviruses, including AIDS. The Journal provides the broadest coverage from molecular biology to clinical studies and outcomes research, focusing on developments in prevention science, novel therapeutics, and immune-restorative approaches. Cutting-edge papers on the latest progress and research advances through clinical trials and examination of targeted antiretroviral agents lead to improvements in translational medicine for optimal treatment outcomes. AIDS Research and Human Retroviruses coverage includes: HIV cure research HIV prevention science - Vaccine research - Systemic and Topical PreP Molecular and cell biology of HIV and SIV Developments in HIV pathogenesis and comorbidities Molecular biology, immunology, and epidemiology of HTLV Pharmacology of HIV therapy Social and behavioral science Rapid publication of emerging sequence information.
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