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Simian Immunodeficiency Virus Rapidly Penetrates the Cervicovaginal Mucosa after Intravaginal Inoculation and Infects Intraepithelial Dendritic Cells

机译:猿猴免疫缺陷病毒在阴道内接种后迅速穿透宫颈阴道粘膜并感染上皮内树突状细胞。

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摘要

Despite recent insights into mucosal human immunodeficiency virus (HIV) transmission, the route used by primate lentiviruses to traverse the stratified squamous epithelium of mucosal surfaces remains undefined. To determine if dendritic cells (DC) are used by primate lentiviruses to traverse the epithelial barrier of the genital tract, rhesus macaques were intravaginally exposed to cell-free simian immunodeficiency virus SIVmac251. We examined formalin-fixed tissues and HLA-DR+-enriched cell suspensions to identify the cells containing SIV RNA in the genital tract and draining lymph nodes within the first 24 h of infection. Using SIV-specific fluorescent in situ hybridization combined with immunofluorescent antibody labeling of lineage-specific cell markers, numerous SIV RNA+ DC were documented in cell suspensions from the vaginal epithelium 18 h after vaginal inoculation. In addition, we determined the minimum time that the SIV inoculum must remain in contact with the genital mucosa for the virus to move from the vaginal lumen into the mucosa. We now show that SIV enters the vaginal mucosa within 60 min of intravaginal exposure, infecting primarily intraepithelial DC and that SIV-infected cells are located in draining lymph nodes within 18 h of intravaginal SIV exposure. The speed with which primate lentiviruses penetrate mucosal surfaces, infect DC, and disseminate to draining lymph nodes poses a serious challenge to HIV vaccine development.
机译:尽管最近有关于粘膜人类免疫缺陷病毒(HIV)传播的见解,但灵长类慢病毒穿越粘膜表面分层鳞状上皮的途径仍然不确定。为了确定灵长类慢病毒是否使用树突状细胞(DC)穿越生殖道的上皮屏障,将恒河猴猕猴阴道内暴露于无细胞猿猴免疫缺陷病毒SIVmac251。我们检查了福尔马林固定的组织和富含HLA-DR +的细胞悬液,以鉴定感染前24小时内生殖道中含有SIV RNA和引流淋巴结的细胞。使用SIV特异性荧光原位杂交与沿袭特异性细胞标记物的免疫荧光抗体标记相结合,在接种阴道后18 h,在来自阴道上皮的细胞悬液中记录了许多SIV RNA + DC。此外,我们确定了SIV接种物必须保持与生殖器粘膜接触的最短时间,以使病毒从阴道腔进入粘膜。我们现在显示SIV在阴道内暴露60分钟内进入阴道粘膜,主要感染上皮内DC,并且SIV感染的细胞位于阴道内SIV暴露18 h内的引流淋巴结中。灵长类慢病毒穿透粘膜表面,感染DC并扩散至引流淋巴结的速度对HIV疫苗的开发提出了严峻挑战。

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