Department of Medical Microbiology and Infectious Diseases, University of Manitoba, Manitoba, Canada.
Department Medical Microbiology, University of Nairobi, Nairobi, Kenya.
Sci Rep. 2017 Sep 11;7(1):11123. doi: 10.1038/s41598-017-11706-y.
CD161 identifies a subset of circulating Th17 cells that are depleted in the blood and gut of HIV-infected individuals. In the female reproductive tract (FRT), the pattern of CD161 expression on CD4 cells remains unknown. Here, we characterized CD161 expression in the FRT of Kenyan female sex workers (FSW). Compared to the blood, CD161CD4 T cells were enriched in the FRT of uninfected FSWs. These cells were depleted in FRT of HIV-infected FSWs. Cervical CD161 cells harboured an activated phenotype (CD69, CD95, HLA-DR) with elevated expression of tissue-homing markers (CCR6, β7 integrin) and HIV co-receptor (CCR5). Mitogen-stimulated production of IL-17 confirmed the Th17 commitment of CD161CD4 T cells in the FRT with a predominance of polyfunctional Th1/Th17 cells. Here, we showed that the expression of CD161 on CD4+T cells is modulated at the FRT, but still identified a highly activated cellular subset, which differentiates into pro-inflammatory Th1/Th17 cells, expresses multiple HIV susceptibility markers and are depleted in HIV-infected individuals. The use of CD161 as a biomarker of HIV targets in the FRT reduces the need for functional assessment of cells and could have important implications in better understanding HIV pathogenesis and Th17 fate in the FRT of high-risk women.
CD161 鉴定了一组循环 Th17 细胞,这些细胞在 HIV 感染者的血液和肠道中耗竭。在女性生殖道(FRT)中,CD4 细胞上 CD161 的表达模式尚不清楚。在这里,我们对肯尼亚性工作者(FSW)的 FRT 中的 CD161 表达进行了特征描述。与血液相比,未感染的 FSW 的 FRT 中 CD161CD4 T 细胞丰富。这些细胞在感染 HIV 的 FSW 的 FRT 中耗竭。宫颈 CD161 细胞具有激活表型(CD69、CD95、HLA-DR),并上调组织归巢标记物(CCR6、β7 整合素)和 HIV 共受体(CCR5)。有丝分裂原刺激产生的 IL-17 证实了 FRT 中 CD161CD4 T 细胞的 Th17 定向,并且以多功能 Th1/Th17 细胞为主。在这里,我们表明 CD4+T 细胞上 CD161 的表达在 FRT 中受到调节,但仍鉴定出一个高度激活的细胞亚群,该亚群分化为促炎 Th1/Th17 细胞,表达多种 HIV 易感性标记物,并在感染 HIV 的个体中耗竭。使用 CD161 作为 FRT 中 HIV 靶标的生物标志物减少了对细胞功能评估的需求,并且可能对更好地理解 HIV 发病机制和高危女性 FRT 中的 Th17 命运具有重要意义。