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精液暴露对女性生殖道免疫和微生物环境的影响。

The Impact of Semen Exposure on the Immune and Microbial Environments of the Female Genital Tract.

作者信息

Jewanraj Janine, Ngcapu Sinaye, Osman Farzana, Mtshali Andile, Singh Ravesh, Mansoor Leila E, Abdool Karim Salim S, Abdool Karim Quarraisha, Passmore Jo-Ann S, Liebenberg Lenine J P

机构信息

Center for the AIDS Programme of Research in South Africa (CAPRISA), Durban, South Africa.

Department of Medical Microbiology, School of Laboratory Medicine and Medical Science, University of KwaZulu-Natal, Durban, South Africa.

出版信息

Front Reprod Health. 2020 Nov 9;2:566559. doi: 10.3389/frph.2020.566559. eCollection 2020.

Abstract

Semen induces an immune response at the female genital tract (FGT) to promote conception. It is also the primary vector for HIV transmission to women during condomless sex. Since genital inflammation and immune activation increase HIV susceptibility in women, semen-induced alterations at the FGT may have implications for HIV risk. Here we investigated the impact of semen exposure, as measured by self-reported condom use and Y-chromosome DNA (YcDNA) detection, on biomarkers of female genital inflammation associated with HIV acquisition. Stored genital specimens were collected biannually (mean 5 visits) from 153 HIV-negative women participating in the CAPRISA 008 tenofovir gel open-label extension trial. YcDNA was detected in cervicovaginal lavage (CVL) pellets by RT-PCR and served as a biomarker of semen exposure within 15 days of genital sampling. Protein concentrations were measured in CVL supernatants by multiplexed ELISA, and the frequency of activated CD4+CCR5+ HIV targets was assessed on cytobrush-derived specimens by flow cytometry. Common sexually transmitted infections (STIs) and bacterial vaginosis (BV)-associated bacteria were measured by PCR. Multivariable linear mixed models were used to assess the relationship between YcDNA detection and biomarkers of inflammation over time. YcDNA was detected at least once in 69% (106/153) of women during the trial (median 2, range 1-5 visits), and was associated with marital status, cohabitation, the frequency of vaginal sex, and Nugent Score. YcDNA detection but not self-reported condom use was associated with elevated concentrations of several cytokines: IL-12p70, IL-10, IFN-γ, IL-13, IP-10, MIG, IL-7, PDGF-BB, SCF, VEGF, β-NGF, and biomarkers of epithelial barrier integrity: MMP-2 and TIMP-4; and with reduced concentrations of IL-18 and MIF. YcDNA detection was not associated with alterations in immune cell frequencies but was related to increased detection of (OR = 1.970; CI 1.309-2.965; = 0.001) at the FGT. YcDNA detection but not self-reported condom use was associated with alterations in cervicovaginal cytokines, BV-associated bacteria, and matrix metalloproteinases, and may have implications for HIV susceptibility in women. This study highlights the discrepancies related to self-reported condom use and the need for routine screening for biomarkers of semen exposure in studies of mucosal immunity to HIV and other STIs.

摘要

精液会在女性生殖道(FGT)引发免疫反应以促进受孕。它也是无保护性行为期间HIV传播给女性的主要媒介。由于生殖器炎症和免疫激活会增加女性对HIV的易感性,精液在FGT引起的变化可能会影响HIV感染风险。在此,我们通过自我报告的避孕套使用情况和Y染色体DNA(YcDNA)检测来衡量精液暴露情况,研究其对与HIV感染相关的女性生殖器炎症生物标志物的影响。每半年(平均5次访视)从153名参与CAPRISA 008替诺福韦凝胶开放标签扩展试验的HIV阴性女性中收集储存的生殖器标本。通过RT-PCR在宫颈阴道灌洗(CVL)沉淀物中检测YcDNA,并将其作为生殖器采样后15天内精液暴露的生物标志物。通过多重ELISA检测CVL上清液中的蛋白质浓度,并通过流式细胞术在细胞刷标本上评估活化的CD4+CCR5+HIV靶标的频率。通过PCR检测常见性传播感染(STIs)和细菌性阴道病(BV)相关细菌。使用多变量线性混合模型评估YcDNA检测与随时间变化的炎症生物标志物之间的关系。在试验期间,69%(106/153)的女性至少有一次检测到YcDNA(中位数为2次,范围为1 - 5次访视),且其与婚姻状况、同居情况、阴道性交频率和 Nugent评分相关。YcDNA检测而非自我报告的避孕套使用情况与几种细胞因子浓度升高有关:IL-12p70、IL-10、IFN-γ、IL-13、IP-10、MIG、IL-7、PDGF-BB、SCF、VEGF、β-NGF,以及上皮屏障完整性生物标志物:MMP-2和TIMP-4;并与IL-18和MIF浓度降低有关。YcDNA检测与免疫细胞频率的改变无关,但与FGT处 (OR = 1.970;CI 1.309 - 2.965; = 0.001)检测增加有关。YcDNA检测而非自我报告的避孕套使用情况与宫颈阴道细胞因子、BV相关细菌和基质金属蛋白酶的改变有关,可能会影响女性对HIV的易感性。这项研究突出了与自我报告的避孕套使用情况相关的差异,以及在HIV和其他性传播感染的黏膜免疫研究中对精液暴露生物标志物进行常规筛查的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ad5/9580648/e3c291691846/frph-02-566559-g0001.jpg

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