Mechanisms of HIV-1 Transmission in the Genital Mucosa of Women
Mechanisms of HIV-1 Transmission in the Genital Mucosa of Women
批准号:
7492011
负责人:
Florian Hladik
金额:
$9.86万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-09-29 至 2008-06-30
关键词:
AddressAntiviral AgentsB-LymphocytesCD4 Positive T LymphocytesCellsContractsDataDendritic CellsDepthEdetic AcidEndocytosisEpithelialEpitheliumEvaluationEventExocervixGenital systemHIVHIV InfectionsHIV-1HeterosexualsHumanIn SituIndividualInfectionIntestinesInvestigationLangerhans cellLife Cycle StagesLocal MicrobicidesMeasuresMedicalModelingMucous MembraneOperative Surgical ProceduresOrgan Culture TechniquesPathway interactionsPrevention strategyPreventiveSexual TransmissionSiteStagingSuctionT-LymphocyteTestingTissuesVaccine DesignVaccinesVacuumVaginaVariantViralVirionVirusWomanabstractingbasedesignintraepithelialmicrobicidemucosal vaccinenonhuman primatenovelpre-clinicalrectaltransmission processvaginal transmission
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Almost 60% of the 40 million HIV-1 infected individuals worldwide are women, and most new HIV-1
infections are contracted by heterosexual contact. Mucosal HIV transmission is therefore the most important
target for preventative strategies. To design vaccines or topical microbicides that interfere with viral
transmission, it is critical to have an in-depth understanding of the initial infection events in the mucosa.
However, the exact pathways whereby HIV enters and propagates in the mucosa remain ill defined. In
particular, data are lacking that clarify how HIV interacts with Langerhans and CD4+ T cells that reside in the
outer epithelial layer of the human vagina or ectocervix. These cells are presumably the first susceptible
targets for HIV, and a successful blockade of their infection could be extremely effective in aborting viral
transmission. To address these issues, we developed a novel ex vivo organ culture model of the human
vaginal mucosa. This model allows us to perform detailed in situ investigations of the productive and non-
productive pathways for entry of HIV into intraepithelial Langerhans and T cells. In Aim 1, we will use our
model to characterize the initial HIV-1 infection steps in these cells. We will also test variations of our model
that may allow for higher throughput studies as required for preclinical microbicide evaluation. In Aim 2, we
will determine if infection of intraepithelial Langerhans and T cells constitutes a bottleneck favoring R5- over
X4-tropic HIV-1 strains, therefore contributing to the predominance of R5 viruses during primary HIV
infection. These studies will yield important information that will allow us to better understand mucosal HIV-1
transmission and selection, and will thus be useful for vaccine and microbicide design.
Lay abstract:
Worldwide, most HIV infections occur through the linings of the genital or intestinal tract following sexual
contact. Information about the initial infection events at these sites is therefore needed to help in devising
medical strategies for prevention, such as vaccines or locally delivered antiviral drugs. In this proposal, we
will use a novel organ culture model of human vaginal tissue obtained from surgeries to characterize the
entry pathways of HIV during the earliest stages of sexual transmission.
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海外基金