New and Simple Assay to Measure Latent HIV Reservoir Using Deep Sequencing Method
New and Simple Assay to Measure Latent HIV Reservoir Using Deep Sequencing Method
批准号:
8768898
负责人:
Sook-Kyung Lee
金额:
$22.8万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-07-01 至 2016-06-30
关键词:
Biological AssayBloodCD4 Positive T LymphocytesCell fusionCellsChronicDevelopmentEnsureEnzyme-Linked Immunosorbent AssayGene ExpressionGoldHIVHIV InfectionsHIV-1HIV-2Highly Active Antiretroviral TherapyInfectionInterphase CellLeadMeasurementMeasuresMediatingMethodsMinorNucleotidesPatientsPolyethylene GlycolsPopulationProceduresProtocols documentationProvirusesRecordsResidual stateResourcesRestSamplingSequence AnalysisSourceSystemT-Cell ActivationT-LymphocyteTechnologyTimeVariantViralViral GenesViremiaVirusWorkassay developmentbasecell transformationcost effectivedeep sequencingenv Gene Productsimprovedlatent infectionmemory CD4 T lymphocytenext generation sequencingpublic health relevancetat Proteintool
中文摘要
描述(由申请人提供):HIV-1在病毒库中的持久性一直是根除HIV-1的主要障碍。潜伏感染的T细胞是残留低水平病毒血症(LLV)的潜在病毒来源之一,静息记忆CD4+ T细胞的潜伏感染得到了很好的证明。在HAART治疗患者的静息CD4+ T细胞中,已经开发出了量化携带复制能力HIV-1的细胞的检测方法。病毒生长测定是目前测量潜伏HIV-1感染的静止CD4+ T细胞的金标准方法。然而,该试验需要大量从血液中纯化的静息CD4+ T细胞,并且涉及一系列稀释来测量是昂贵和劳动密集型的
英文摘要
DESCRIPTION (provided by applicant): HIV-1 persistence in viral reservoirs has been the major obstacle for the eradication of HIV-1. Latently infected T cells are one of the potential sources of the virus that is found as residual low-level viremia (LLV) and latent infection of resting memory CD4+ T cells is well demonstrated. Assays have been developed to quantify cells that harbor replication-competent HIV-1 among resting CD4+ T cells in patients on HAART. A viral outgrowth assay is the current gold-standard method to measure latently HIV-1 infected resting CD4+ T cells. However, this assay requires large numbers of resting CD4+ T cells purified from blood and is costly and labor- intensive involving a serial dilution to measure
infectious units per million (IUPM) resting CD4+ T cells. To overcome the issues with the current assay, in this application we propose an assay based on next- generation sequencing (NGS) technology. In the proposed assay, the number of different sequences of the viruses bulk-cultured from the resting CD4+ T cells will be directly analyzed to score the number of latently HIV-1-infected CD4+ T cells. Since deep sequencing is highly sensitive to detect multiple variants in a viral population, it will be possible to count the number of distinct viruses that hae been induced to replicate in a bulk culture. These studies will provide valuable information for curing HIV infection and lead to a development of an assay to quantify the latent HIV-1 reservoir with improved accuracy, less time and resource consuming, and less labor intensive.
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