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Unexpected Inflammatory Effects of Intravaginal Gels (Universal Placebo Gel and Nonoxynol-9) on the Upper Female Reproductive Tract: A Randomized Crossover Study

机译:阴道内凝胶(通用安慰剂凝胶和Nonoxynol-9)对上位女性生殖道的意外发炎作用:一项随机交叉研究

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摘要

Intravaginal anti-HIV microbicides could provide women with a self-controlled means for HIV prevention, but results from clinical trials have been largely disappointing. We postulated that unrecognized effects of intravaginal gels on the upper female reproductive tract might contribute to the lower-than-expected efficacy of HIV microbicides. Our objective was to study the effects of intravaginal gels on the immune microenvironment of the cervix and uterus. In this randomized crossover study, 27 healthy female volunteers used a nightly application of intravaginal nonoxynol-9 (N9) gel as a “failed” microbicide or the universal placebo gel (UPG) as a “safe” gel (intervention cycles), or nothing (control cycle) from the end of menses to the mid-luteal phase. At a specific time-point following ovulation, all participants underwent sample collection for measurements of T-cell phenotypes, gene expression, and cytokine/chemokine protein concentrations from 3 anatomic sites above the vagina: the cervical transformation zone, the endocervix and the endometrium. We used hierarchical statistical models to estimate mean (95% CI) intervention effects, for N9 and UPG relative to control. Exposure to N9 gel and UPG generated a common “harm signal” that included transcriptional up-regulation of inflammatory genes chemokine (C-C motif) ligand 20 (macrophage inflammatory factor-3alpha) and interleukin 8 in the cervix, decreased protein concentrations of secretory leukocyte protease inhibitor, and transcriptional up-regulation of inflammatory mediators glycodelin-A and osteopontin in the endometrium. These results need to be replicated with a larger sample, but underscore the need to consider the effects of microbicide agents and gel excipients on the upper female reproductive tract in studies of vaginal microbicides.
机译:阴道内抗HIV杀微生物剂可以为妇女提供自我控制的HIV预防手段,但是临床试验的结果令人大失所望。我们推测阴道内凝胶对女性上生殖道的无法识别的作用可能会导致HIV杀菌剂的功效低于预期。我们的目的是研究阴道内凝胶对子宫颈和子宫的免疫微环境的影响。在这项随机交叉研究中,有27位健康的女性志愿者每晚使用阴道内的壬氧基9(N9)凝胶作为“失败的”杀微生物剂,或将通用安慰剂凝胶(UPG)作为“安全”的凝胶(干预周期)使用,或不使用(控制周期)从月经结束到黄体中期。在排卵后的特定时间点,对所有参与者进行样本采集,以测量阴道上方3个解剖部位(宫颈转化区,宫颈内膜和子宫内膜)的T细胞表型,基因表达和细胞因子/趋化因子蛋白浓度。我们使用分层统计模型来估计相对于对照的N9和UPG的平均干预效果(95%CI)。暴露于N9凝胶和UPG会产生一个常见的“危害信号”,包括子宫颈中炎症基因趋化因子(CC基序)配体20(巨噬细胞炎性因子3α)和白介素8的转录上调,分泌性白细胞蛋白酶蛋白浓度降低子宫内膜炎性介质糖蛋白A和骨桥蛋白的抑制剂和转录上调。这些结果需要与更大的样本重复,但强调在阴道杀菌剂研究中需要考虑杀菌剂和凝胶赋形剂对女性上生殖道的影响。

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