Project 2: Revealing Viral Population and Host Environment Dynamics of SIV Tissue Reservoir

项目2：揭示SIV组织库的病毒种群和宿主环境动态

基本信息

批准号：
10666587
负责人：
Ramon Lorenzo-Redondo
金额：
$ 24.46万
依托单位：
NORTHWESTERN UNIVERSITY AT CHICAGO
依托单位国家：
美国
项目类别：
财政年份：
2022
资助国家：
美国
起止时间：
2022-07-15 至 2027-04-30
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10666587
关键词：
Anatomy Antigens Binding Biological Process Biology Blood specimen Cells Characteristics Clonal Expansion Data Detection Dimensions Environment Evaluation Event Future Gene Expression Gene Expression Profile Genetic Transcription Genome Genomics HIV HIV-1 Immune Immune response Individual Infection Interruption Knowledge acquisition Label Laboratories Laboratory Finding Lead Lymphoid Tissue Macaca Macaca mulatta Methods Modeling Mucous Membrane Nature PET/CT scan Phylogenetic Analysis Play Population Population Characteristics Population Dynamics Population Sizes Predisposition Process Production Property Research Design Residual state Role SIV Sampling Signal Transduction Site Source Surveys System Techniques Tissue Sample Tissues Update Viral Viral Genes Viral reservoir Viremia Virus Virus Replication X-Ray Computed Tomography antiretroviral therapy biological systems cell type chronic infection design env Gene Products experimental study in vivo insight mast cell novel single cell analysis spatiotemporal study characteristics success transcriptome sequencing transcriptomics viral detection viral rebound virus characteristic virus envelope virus host interaction

项目摘要

PROJECT SUMMARY/ABSTRACT Despite the remarkable success of the combination antiretroviral therapy (cART) to control HIV-1 infection, viral reservoirs persist indefinitely under treatment. These remaining viral populations constitute the principal burden for an effective HIV-1 cure, as they lead to a rapid rebound in viremia when treatment fails or after analytic treatment interruption (ATI). Unfortunately, our understanding of the mechanisms of HIV-1 persistence during cART is limited because the viral reservoir population size is very small and it is established within a wide variety of susceptible tissues, inaccessible to evaluation. Hence these difficulties, the majority of the reservoir studies do not include tissue samples or study a very limited sampling of the tissue reservoirs. Therefore, we are not able to properly study these viral populations and their main characteristics remain unknown. Understanding the nature and properties of these tissue reservoirs during treatment is key to design a successful HIV-1 cure strategy. The team comprised by the Hope lab and Dr. Villinger has optimized and refined their 89Zr-labelled FAB2 probe that allows for the in vivo detection of cells expressing SIV env in an infected macaque. Using this approach, they have generated a new PET-CT-based workflow for the identification and downstream characterization of foci of SIV infection in tissues. This updated “beacon-guided system” is exquisitely sensitive and it is extremely powerful to find and characterize small foci of infected cells during cART or early after ATI, prior to any detectable viremia. These foci represent extremely rare events that are key to the understanding of underlying SIV biology and yet, to date, were only found through random and/or biased survey of tissue. In the current proposal, we intend to use the Hope lab ability to localize SIV active viremia sites in infected macaques and complementary genomic analysis workflows optimized by our team, to perform in-depth spatio-temporal studies of the reservoir viral population dynamics. We will use phylogenetic, evolutionary, and phyloanatomy analysis to study the characteristics tissue reservoirs. We will also assess the contribution of biological processes such as clonal expansion, residual viral replication, and viral production bursts in the process of reservoir persistence during cART. Additionally, we will analyze the characteristics and transcriptional profiles of the different cell types that harbor the reservoir in tissues using our multiple complementary genomic techniques. We will use PET-CT-guided RNAseq and PET-CT-guided spatial transcriptomics from SIV positive tissues, and isolate specific types of infected cells to analyze their transcriptional profiles using single-cell analysis. Due to Hope lab’s findings indicating that mast cells could be key in the reservoir persistence, we plan to specifically study the role of these mast cells in the viral population dynamics of the tissue reservoirs. By following this multidimensional approach, we will define with unprecedented detail the main properties of the cells in tissues that harbor the reservoir during treatment and are the initial source of the rebounding virus when treatment is interrupted.

项目概要/摘要尽管联合抗逆转录病毒疗法 (cART) 在控制 HIV-1 感染方面取得了显著成功，但病毒这些剩余的病毒种群在治疗过程中会无限期地持续存在。有效治愈 HIV-1，因为当治疗失败或分析后，它们会导致病毒血症迅速反弹不幸的是，我们对 HIV-1 持续存在机制的了解还不够。 cART 是有限的，因为病毒库群体规模非常小，而且它是在多种病毒中建立的因此，大多数储库研究都存在这些困难。不包括组织样本或研究非常有限的组织储存库样本，因此，我们不这样做。能够正确研究这些病毒种群，但它们的主要特征仍然未知。治疗期间这些组织储存库的性质和特性是设计成功的 HIV-1 治疗方法的关键由 Hope 实验室和 Villinger 博士组成的团队优化并完善了他们的 89Zr 标记。 FAB2 探针可用于体内检测受感染的猕猴中表达 SIV env 的细胞。方法，他们生成了一个新的基于 PET-CT 的工作流程，用于识别和下游这种更新的“信标引导系统”非常敏感。在 cART 期间或 ATI 后早期发现和表征受感染细胞的小病灶非常强大，在任何可检测到的病毒血症之前，这些病灶代表了极其罕见的事件，这对于理解病毒血症至关重要。 SIV 的生物学基础，但迄今为止，只能通过随机和/或有偏见的组织调查来发现。目前的提案，我们打算利用 Hope 实验室的能力来定位受感染猕猴中的 SIV 活性病毒血症位点以及我们团队优化的补充基因组分析工作流程，以执行深入的时空分析我们将使用系统发育、进化和系统解剖学来研究储存病毒种群动态。我们还将评估生物过程的贡献。例如克隆扩增、残留病毒复制以及储存过程中的病毒产量爆发此外，我们将分析 cART 期间的持久性。使用我们的多种互补基因组技术，在组织中储存储存库的不同细胞类型。我们将使用 PET-CT 引导的 RNAseq 和 PET-CT 引导的 SIV 阳性组织的空间转录组学，以及使用单细胞分析分离特定类型的感染细胞以分析其转录谱。希望实验室的研究结果表明肥大细胞可能是储存库持久性的关键，我们计划专门通过遵循这一点，研究这些肥大细胞在组织储存库的病毒群体动态中的作用。多维方法，我们将以前所未有的细节定义组织中细胞的主要特性在治疗期间隐藏着病毒储存库，并且是治疗时病毒反弹的最初来源打断了。