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通过创新的 scRNAseq 分析管道鉴定单核细胞、HIV 和 ART 的相互作用:与 HIV 相关的储库和合并症的途径。

Interactions of Monocytes, HIV, and ART Identified by an Innovative scRNAseq Pipeline: Pathways to Reservoirs and HIV-Associated Comorbidities.

机构信息

Department of Pathology, Albert Einstein College of Medicine, Bronx, New York, USA.

Department of Neurological Sciences, University of Nebraska Medical Center, Omaha, Nebraska, USA.

出版信息

mBio. 2020 Jul 28;11(4):e01037-20. doi: 10.1128/mBio.01037-20.

Abstract

HIV reservoirs persist despite successful antiretroviral therapy (ART) and are a major obstacle to the eradication and cure of HIV. The mature monocyte subset, CD14CD16, contributes to viral reservoirs and HIV-associated comorbidities. Only a subset of monocytes harbors HIV (HIV), while the rest remain uninfected, exposed cells (HIV). We developed an innovative single cell RNA sequencing (scRNAseq) pipeline that detects HIV and host transcripts simultaneously, enabling us to examine differences between HIV and HIV mature monocytes. Using this, we characterized uninfected, HIV, and HIV primary human mature monocytes with and without ART. We showed that HIV mature monocytes do not form their own cluster separately from HIV but can be distinguished by significant differential gene expression. We found that ART decreased levels of unspliced HIV transcripts potentially by modulating host transcriptional regulators shown to decrease viral infection and replication. We also identified and characterized mature monocyte subpopulations differentially impacted by HIV and ART. We identified genes dysregulated by ART in HIV monocytes compared to their uninfected counterpart and, of interest, the junctional protein ALCAM, suggesting that ART impacts monocyte functions. Our data provide a novel method for simultaneous detection of HIV and host transcripts. We identify potential targets, such as those genes whose expression is increased in HIV mature monocytes compared to HIV, to block their entry into tissues, preventing establishment/replenishment of HIV reservoirs even with ART, thereby reducing and/or eliminating viral burden and HIV-associated comorbidities. Our data also highlight the heterogeneity of mature monocyte subsets and their potential contributions to HIV pathogenesis in the ART era. HIV enters tissues early after infection, leading to establishment and persistence of HIV reservoirs despite antiretroviral therapy (ART). Viral reservoirs are a major obstacle to the eradication and cure of HIV. CD14CD16 (mature) monocytes may contribute to establishment and reseeding of reservoirs. A subset of monocytes, consisting mainly of CD14CD16 cells, harbors HIV (HIV), while the rest remain uninfected, exposed cells (HIV). It is important to identify cells harboring virus to eliminate reservoirs. Using an innovative single-cell RNA sequencing (scRNAseq) pipeline to detect HIV and host transcripts simultaneously, we characterized HIV and HIV primary human mature monocytes with and without ART. HIV mature monocytes are not a unique subpopulation but rather can be distinguished from HIV by differential gene expression. We characterized mature monocyte subpopulations differently impacted by HIV and ART, highlighting their potential contributions to HIV-associated comorbidities. Our data propose therapeutic targets to block HIV monocyte entry into tissues, preventing establishment and replenishment of reservoirs even with ART.

摘要

尽管抗逆转录病毒疗法(ART)取得了成功,但 HIV 储存库仍然存在,这是 HIV 根除和治愈的主要障碍。成熟的单核细胞亚群 CD14CD16 有助于病毒储存库的形成和与 HIV 相关的合并症。只有一部分单核细胞携带 HIV(HIV),而其余的则保持未感染、暴露的细胞(HIV)。我们开发了一种创新的单细胞 RNA 测序(scRNAseq)管道,可同时检测 HIV 和宿主转录本,使我们能够检查 HIV 和 HIV 成熟单核细胞之间的差异。使用这种方法,我们对有和没有 ART 的未感染、HIV 和 HIV 原发性人成熟单核细胞进行了特征描述。我们表明,HIV 成熟单核细胞不会与 HIV 分开形成自己的簇,但可以通过显著的差异基因表达来区分。我们发现,ART 通过调节宿主转录调节剂来降低未剪接 HIV 转录本的水平,这些调节剂已被证明可降低病毒感染和复制。我们还鉴定并描述了受 HIV 和 ART 影响不同的成熟单核细胞亚群。我们在 HIV 单核细胞中鉴定了与未感染对照相比受 ART 调节的基因,并发现了有趣的 junctophilin ALCAM,表明 ART 影响单核细胞功能。我们的数据提供了一种同时检测 HIV 和宿主转录本的新方法。我们确定了一些潜在的靶点,例如与 HIV 相比在 HIV 成熟单核细胞中表达增加的基因,以阻止它们进入组织,从而防止 HIV 储存库的建立/补充,即使在接受 ART 的情况下,也能降低和/或消除病毒载量和与 HIV 相关的合并症。我们的数据还突出了成熟单核细胞亚群的异质性及其在 ART 时代对 HIV 发病机制的潜在贡献。HIV 在感染后早期进入组织,导致尽管进行了抗逆转录病毒治疗(ART),但 HIV 储存库仍得以建立和持续存在。病毒储存库是 HIV 根除和治愈的主要障碍。CD14CD16(成熟)单核细胞可能有助于储存库的建立和再播种。一组主要由 CD14CD16 细胞组成的单核细胞携带 HIV(HIV),而其余的则保持未感染、暴露的细胞(HIV)。确定携带病毒的细胞对于消除储存库很重要。我们使用创新的单细胞 RNA 测序(scRNAseq)管道同时检测 HIV 和宿主转录本,对有和没有 ART 的 HIV 和 HIV 原发性人成熟单核细胞进行了特征描述。HIV 成熟单核细胞不是一个独特的亚群,而是可以通过差异基因表达与 HIV 区分开来。我们描述了受 HIV 和 ART 不同影响的成熟单核细胞亚群,突出了它们对与 HIV 相关的合并症的潜在贡献。我们的数据提出了治疗靶点,以阻止 HIV 单核细胞进入组织,防止即使在接受 ART 的情况下储存库的建立和补充。

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