Thurman Andrea Ries, Yousefieh Nazita, Chandra Neelima, Kimble Thomas, Asin Susana, Rollenhagen Christiane, Anderson Sharon M, Herold Betsy C, Freiermuth Jamie L, Starkman Brian S, Mesquita Pedro M M, Richardson-Harman Nicola, Cunningham Tina, Hillier Sharon, Rabe Lorna, Schwartz Jill L, Doncel Gustavo F
1 CONRAD Clinical Research Center , Eastern Virginia Medical School, Norfolk, Virginia.
2 V.A. Medical Center , White River Junction, Vermont.
AIDS Res Hum Retroviruses. 2017 Aug;33(8):807-819. doi: 10.1089/AID.2016.0320. Epub 2017 May 16.
The objective of this study was to characterize cervicovaginal (CV) mucosal factors modulating susceptibility to human immunodeficiency virus (HIV) acquisition in healthy premenopausal (PRE) and postmenopausal (POST) women before and after treatment with estradiol (E2). We compared CV mucosal epithelial histology and immune cells, vaginal microbiota, antimicrobial activity of and soluble mucosal protein concentrations in the CV fluid lavage (CVL), and p24 antigen production after ex vivo infection of ectocervical tissues with HIV-1 among PRE women (n = 20) in the follicular and luteal phases of the menstrual cycle and POST women (n = 17) at baseline and after ∼1 month of treatment with 0.01% vaginal E2 cream. Compared to PRE women, we measured higher levels of p24 antigen after ex vivo infection in tissues from POST women. POST women had a significantly thinner vaginal epithelium with decreased tight junction proteins and a higher density of mucosal immune T cells and lower levels of CD1a antigen-presenting cells, antimicrobial peptides, and inflammatory cytokines in the CVL (p values <.05). POST women had higher vaginal pH and lower vaginal Lactobacilli (p values <.05) than PRE women. After vaginal E2 therapy, CV endpoints and ex vivo HIV replication in POST tissues were similar to those observed in PRE tissues. The CV mucosa in POST women is thinned and compromised, with increased HIV-target immune cells and decreased antimicrobial factors, being more susceptible to HIV infection. After POST women receive topical E2 treatment, mucosal endpoints are similar to PRE levels.
本研究的目的是表征在健康的绝经前(PRE)和绝经后(POST)女性中,在接受雌二醇(E2)治疗前后,调节获得人类免疫缺陷病毒(HIV)易感性的宫颈阴道(CV)黏膜因子。我们比较了CV黏膜上皮组织学和免疫细胞、阴道微生物群、CV冲洗液(CVL)中的抗菌活性和可溶性黏膜蛋白浓度,以及月经周期卵泡期和黄体期的PRE女性(n = 20)以及基线时和在用0.01%阴道E2乳膏治疗约1个月后的POST女性(n = 17)的宫颈外组织经HIV-1体外感染后的p24抗原产生情况。与PRE女性相比,我们在POST女性组织的体外感染后测量到更高水平的p24抗原。POST女性的阴道上皮明显更薄,紧密连接蛋白减少,黏膜免疫T细胞密度更高,CVL中CD1a抗原呈递细胞、抗菌肽和炎性细胞因子水平更低(p值<.05)。POST女性的阴道pH值高于PRE女性,阴道乳酸杆菌水平低于PRE女性(p值<.05)。阴道E2治疗后,POST组织中的CV终点指标和体外HIV复制情况与PRE组织中观察到的相似。POST女性的CV黏膜变薄且受损,HIV靶向免疫细胞增加,抗菌因子减少,更容易感染HIV。POST女性接受局部E2治疗后,黏膜终点指标与PRE水平相似。