IPDA for High-Priority HIV-1 Subtype C to Enable Global Eradication Trials
IPDA for High-Priority HIV-1 Subtype C to Enable Global Eradication Trials
批准号:
10445356
负责人:
Gregory Michael Laird
金额:
$30.0万
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
已结题
起止时间:
2021-07-07 至 2024-06-30
关键词:
AIDS/HIV problemAcquired Immunodeficiency SyndromeAddressAdultAfricaAfricanAnti-Retroviral AgentsBase SequenceBenchmarkingBiological AssayCD4 Positive T LymphocytesCellsClinicalCohort AnalysisCohort StudiesCollaborationsCryopreservationDNADataDevelopmentDiagnosticDisease remissionEuropeFrequenciesGenerationsGenomic DNAHIVHIV-1ImmuneImmune systemIndividualInfectionLeftLegal patentLengthLettersLibrariesLifeMeasurementMeasuresMediatingMilitary PersonnelMolecularMolecular WeightMonitorNational Institute of Allergy and Infectious DiseaseParticipantPatternPerformancePeripheral Blood Mononuclear CellPersonsPharmaceutical PreparationsPhasePopulationPositioning AttributePrevalenceProvirusesPublic HealthPublishingRegimenReproducibilityResearchRestRetroviridaeSamplingSampling StudiesSiteSmall Business Innovation Research GrantSpecificityTestingTimeTissuesTreatment EfficacyUnited StatesUnited States National Institutes of HealthViralViral Load resultViral reservoirViremiaVirusVirus Replicationantiretroviral therapybasecohortdesigndigitalgenome sequencingindexinglongitudinal analysismemory CD4 T lymphocytenovelperipheral bloodprogramsresearch clinical testingside effectsuccesstherapeutic target
中文摘要
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英文摘要
PROJECT SUMMARY/ABSTRACT
Human immunodeficiency virus type-1 (HIV-1) is a retrovirus that infects CD4+ T cells of the immune
system. If left untreated, HIV-1 infected individuals will progress to AIDS and may ultimately die as a result.
Combination antiretroviral therapy is extremely effective at stopping the replication of HIV-1 in infected
individuals. Despite the success of this therapy at suppressing HIV-1 replication to clinically undetectable
levels, antiretroviral therapy is not curative. This is due to the persistence of HIV-1 in a silent, or latent, state
within a subset of CD4+ T cells known as resting memory CD4+ T cells. In this latent state, these infected cells
are not targeted by antiretroviral drugs and cannot be eliminated by the immune system. In HIV-1 infected
individuals, latently infected CD4+ T cells are found at extremely low frequencies (~1 per million resting
memory CD4+ T cells), with the majority found within immune tissues at any given time. This population of
latently infected cells is very stable, demanding that HIV-1 infected individuals remain on antiretroviral therapy
indefinitely to avoid rebound of viremia. As such, this population of latently infected CD4+ T cells is the main
barrier to curing HIV-1 infection.
Developing strategies to eliminate latently infected cells is a major focus of the NIH, NIAID, and the
HIV-1 research field. To demonstrate the efficacy of therapeutics targeting the latent reservoir, we must be
able to measure the frequency of latently infected cells using rapid and accurate assays that can be scaled for
widespread clinical use. Critically, such assays must be capable of accurately measuring the size of the latent
reservoir across viral subtypes. Accelevir Diagnostics, LLC has recently developed the IPDA as a novel digital
droplet PCR assay to measure intact and defective proviruses in a small sample of peripheral blood. The IPDA
was optimized for use in people with subtype B HIV-1 infection, which predominates in the United States and
Europe but comprises on a small fraction of people living with HIV-1 worldwide. In this proposal, Accelevir
Diagnostics seeks to expand the IPDA coverage to include people living with subtype C HIV-1 infection, which
accounts for approximately 50% of all people living with HIV-1 worldwide. Broadly, this proposal aims to
perform in-depth proviral sequencing to inform expansion of assay coverage followed by assay design
adaptation, performance qualification, and analysis of longitudinally collected samples from people living with
subtype C HIV-1 infection. This proposal leverages a close collaboration with the US Military HIV Research
Program, enabling access to a unique and cohort of people living with subtype C HIV-1 infection across Africa.
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批准号:10324540
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项目类别:
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资助金额:$30.0万
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财政年份:2021
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负责人:Gregory Michael Laird
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依托单位:
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项目类别:
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资助金额:$30.0万
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负责人:Gregory Michael Laird
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财政年份:2015
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依托单位:
海外基金