The Early Events Determining SIV Rectal Transmission
The Early Events Determining SIV Rectal Transmission
批准号:
8310089
负责人:
Qingsheng Li
金额:
$29.55万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-08-15 至 2014-07-31
关键词:
AddressAnatomyAnusBloodCD4 Positive T LymphocytesCD8B1 geneCellsCervicalCervix UteriColonDendritic CellsDevelopmentDistalEffector CellEventHIV-1Host DefenseImmune responseImmune systemIn SituIn Situ HybridizationInfectionInflammationInterventionKnowledgeLamina PropriaLeadLocal MicrobicidesLocationLymphoidLymphoid TissueMacaca mulattaModelingPhysiologicalPlayProceduresPublic HealthRaceRectumResearchRoleSIVSiteSpatial DistributionSystemic infectionT-LymphocyteTestingTimeTissuesVaccinesVaginaVirusVirus Replicationcell typedesigninnovationinsightmacrophagemen who have sex with menmicrobicidenovelpreventrectalresponsespatial relationshiptransmission processvaginal transmission
中文摘要
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英文摘要
Although anal intercourse is a common mode of HIV-1 transmission, particularly for men who have sex with men, many fundamental and mechanistic questions remain. The long-term objective of this study is to understand the early events in HIV-1 rectal transmission and to gain new insights, which will potentially lead to new intervention strategies, including vaccines and topical microbicides optimized for rectal use. Studying HIV-1 vaginal transmission in the highly relevant SIV-rhesus macaque model has revealed important events critical for transmission, such as target cell availability, innate immune response, and inflammation at the portal of entry, all factors which play a key role in transmission. Because the anatomical/histological features and the physiological functions of vagina and cervix differ from the rectum, we hypothesize that the underlying mechanisms and timing of HIV-1 rectal transmission will significantly differ from those of vaginal-cervical transmission. Utilizing innovative approaches and an established conceptual framework from studies of vaginal transmission, we will test this hypothesis by investigating three specific aims: 1) determine the timing, location, spatial distribution and cell types of virus-infected cells at the portal of entry and in draining and distal lymphatic tissues; 2) determine relationships between virus and susceptible target cells (CD4+ T cells, macrophages, and dendritic cells) and between virus-infected cells and the mucosal innate immune response in the rectum shortly after intra-rectal SIV inoculation, thereby determining whether changes in target-cell availability play a critical role in local expansion and systemic spread of infection; and 3) determine the spatial relationships and ratio of virus-specific CD8+ T effector cells (E) and virus-infected-target cells (T) at the portal of entry and in other tissue compartments to extent of control of virus replication, using a novel procedure combining in-situ tetramers and in-situ hybridization The proposed research is significant as it is expected to reveal important mechanisms underlying rectal transmission and potentially provide guidance for designing anti-HIV-1 vaccines and topical microbicides.
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The Early Events Determining SIV Rectal Transmission
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