Tasker Carley, Roche Natalie E, Lo Yungtai, Chang Theresa L
Public Health Research Institute, Rutgers, New Jersey Medical School, 225 Warren Street, Newark, NJ 07103, USA.
Department of Microbiology, Biochemistry and Molecular Genetics, Rutgers, New Jersey Medical School, Newark, NJ 07103, USA.
Viruses. 2025 Sep 22;17(9):1283. doi: 10.3390/v17091283.
Depot medroxyprogesterone acetate (Depo-Provera) has been associated with an increased risk of HIV acquisition. We have previously shown that Depo-Provera administration increases immune markers for HIV preference on peripheral and cervical CD4 T cells but decreases the levels of most immune mediators at vaginal and cervical mucosa. In this study, we determined the effect of cervicovaginal secretions from women before (visit 1), one month (visit 2) and three months (visit 3) after Depo-Provera treatment on HIV infectivity ex vivo. The effect of supernatants from vaginal, endocervical, and rectal swabs and from cervical cytobrush on HIV infectivity were assessed by a single-cycle infection assay using CCR5-using HIV-luciferase reporter viruses. We found that endocervical secretions from women after Depo-Provera treatment promoted HIV infectivity. When analyzing the association between endocervical mediator changes in response to Depo-Provera, available in our previous study, and the changes in HIV infectivity pre- and post-treatment, we found that changes in IL-17 and VEGF were positively associated with changes in HIV infectivity at visit 2 compared with visit 1, whereas changes in RANTES and IL-4 were negatively associated with HIV infectivity. The negative association between RANTES and HIV infectivity was also observed at visit 3 compared with visit 1. Additionally, changes in IL-1α at visit 3 were positively associated with changes in HIV infectivity compared with visit 1. These findings suggest that Depo-Provera may increase the HIV risk by shifting the mucosal milieu that promotes HIV infectivity.
醋酸甲羟孕酮长效注射剂(狄波 - 普维拉)与感染艾滋病毒的风险增加有关。我们之前已经表明,给予狄波 - 普维拉会增加外周血和宫颈CD4 T细胞上艾滋病毒偏好的免疫标志物,但会降低阴道和宫颈黏膜处大多数免疫介质的水平。在本研究中,我们测定了狄波 - 普维拉治疗前(第1次就诊)、治疗后1个月(第2次就诊)和3个月(第3次就诊)的女性宫颈阴道分泌物对艾滋病毒体外感染性的影响。通过使用依赖CCR5的艾滋病毒 - 荧光素酶报告病毒的单循环感染试验,评估阴道、宫颈管内膜和直肠拭子以及宫颈细胞刷的上清液对艾滋病毒感染性的影响。我们发现,狄波 - 普维拉治疗后的女性宫颈管内膜分泌物促进了艾滋病毒的感染性。在分析我们之前研究中可获得的宫颈管内膜介质对狄波 -普维拉反应的变化与治疗前后艾滋病毒感染性变化之间的关联时,我们发现,与第1次就诊相比,第2次就诊时IL - 17和VEGF的变化与艾滋病毒感染性的变化呈正相关,而RANTES和IL - 4的变化与艾滋病毒感染性呈负相关。与第1次就诊相比,在第3次就诊时也观察到RANTES与艾滋病毒感染性之间的负相关。此外,与第1次就诊相比,第3次就诊时IL - 1α的变化与艾滋病毒感染性的变化呈正相关。这些发现表明,狄波 - 普维拉可能通过改变促进艾滋病毒感染性的黏膜环境来增加感染艾滋病毒的风险。