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与接受抗逆转录病毒治疗的 HIV 感染者的 HIV DNA 储存库大小相关的免疫和病毒学参数。

Immunologic and Virologic Parameters Associated With Human Immunodeficiency Virus (HIV) DNA Reservoir Size in People With HIV Receiving Antiretroviral Therapy.

机构信息

Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases (NIAID).

Critical Care Medicine Department, Clinical Center, NIH, Bethesda, Maryland.

出版信息

J Infect Dis. 2024 Jun 14;229(6):1770-1780. doi: 10.1093/infdis/jiad595.

Abstract

BACKGROUND

A better understanding of the dynamics of human immunodeficiency virus (HIV) reservoirs in CD4+ T cells of people with HIV (PWH) receiving antiretroviral therapy (ART) is crucial for developing therapies to eradicate the virus.

METHODS

We conducted a study involving 28 aviremic PWH receiving ART with high and low levels of HIV DNA. We analyzed immunologic and virologic parameters and their association with the HIV reservoir size.

RESULTS

The frequency of CD4+ T cells carrying HIV DNA was associated with higher pre-ART plasma viremia, lower pre-ART CD4+ T-cell counts, and lower pre-ART CD4/CD8 ratios. During ART, the High group maintained elevated levels of intact HIV proviral DNA, cell-associated HIV RNA, and inducible virion-associated HIV RNA. HIV sequence analysis showed no evidence for preferential accumulation of defective proviruses nor higher frequencies of clonal expansion in the High versus Low group. Phenotypic and functional T-cell analyses did not show enhanced immune-mediated virologic control in the Low versus High group. Of considerable interest, pre-ART innate immunity was significantly higher in the Low versus High group.

CONCLUSIONS

Our data suggest that innate immunity at the time of ART initiation may play an important role in modulating the dynamics and persistence of viral reservoirs in PWH.

摘要

背景

深入了解接受抗逆转录病毒疗法 (ART) 的人类免疫缺陷病毒 (HIV) 感染者 (PWH) 中 CD4+ T 细胞中 HIV 储库的动态变化对于开发清除病毒的疗法至关重要。

方法

我们进行了一项研究,纳入了 28 名接受 ART 治疗且 HIV DNA 水平高低不同的无病毒血症 PWH。我们分析了免疫和病毒学参数及其与 HIV 储库大小的关系。

结果

携带 HIV DNA 的 CD4+ T 细胞的频率与较高的 ART 前血浆病毒载量、较低的 ART 前 CD4+ T 细胞计数和较低的 ART 前 CD4/CD8 比值相关。在 ART 期间,高组维持高水平的完整 HIV 前病毒 DNA、细胞相关 HIV RNA 和诱导的病毒相关 HIV RNA。HIV 序列分析未显示出有利于缺陷前病毒积累的证据,也未显示高组比低组中克隆扩增的频率更高。表型和功能 T 细胞分析并未显示低组比高组中增强的免疫介导的病毒控制。值得注意的是,低组比高组的 ART 前先天免疫显著更高。

结论

我们的数据表明,ART 起始时的先天免疫可能在调节 PWH 中病毒储库的动态和持久性方面发挥重要作用。

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