Sheng Qunying, Cui Xiaojie, Zhang Junneng, Yang Fang, Zeng Lingqian
Department of Gynecology, the Fifth Hospital of Xiamen, Xiamen, Fujian, 361101, People's Republic of China.
Department of Clinical Laboratory, the Fifth Hospital of Xiamen, Xiamen, Fujian, 361101, People's Republic of China.
Int J Gen Med. 2025 Aug 24;18:4683-4693. doi: 10.2147/IJGM.S545252. eCollection 2025.
Human papillomavirus (HPV) infection is essential for cervical cancer (CC) development, yet only a fraction of infections persist and progress. Vaginal microecology and immune responses may play pivotal roles in determining HPV outcomes. This study aimed to explore the association between vaginal microecological alterations, immune-inflammatory markers, and the natural course of HPV infection.
We retrospectively analyzed 312 women undergoing HPV genotyping, vaginal microecological evaluation, and cytokine profiling over a two-year period. Logistic regression and ROC curve analyses were used to identify predictors of HPV persistence or clearance.
HPV-positive women exhibited significantly higher rates of elevated vaginal pH (76.2%), bacterial vaginosis (37.1%), reduced hydrogen peroxide production (41.0%), sialidase activity (33.3%), and Community state type IV (CST IV) dominance (34.3%) compared to HPV-negative women (P<0.001). Multivariate analysis revealed elevated pH, Nugent score ≥ 7, negative HO production, CST IV, biofilm formation, and high IL-6 levels as independent predictors of HPV persistence. ROC analysis showed the combined predictive model achieved an AUC of 0.842. Kaplan-Meier survival analysis indicated that women with normal vaginal microecology had significantly higher HPV clearance rates at 24 months (90.1%) compared to those with dysbiosis (66.2%, P<0.001). Additionally, persistent infections were associated with elevated TNF-α, reduced IL-12, higher CRP, and oxidative stress markers.
Vaginal microecological imbalance and immune dysregulation are major determinants of HPV persistence. Comprehensive assessment of these factors may improve risk stratification and guide individualized interventions for HPV-infected women.
人乳头瘤病毒(HPV)感染是宫颈癌(CC)发生的必要条件,但只有一小部分感染会持续存在并进展。阴道微生态和免疫反应可能在决定HPV感染结局中起关键作用。本研究旨在探讨阴道微生态改变、免疫炎症标志物与HPV感染自然病程之间的关联。
我们回顾性分析了312名在两年期间接受HPV基因分型、阴道微生态评估和细胞因子分析的女性。采用逻辑回归和ROC曲线分析来确定HPV持续感染或清除的预测因素。
与HPV阴性女性相比,HPV阳性女性的阴道pH值升高(76.2%)、细菌性阴道病(37.1%)、过氧化氢产生减少(41.0%)、唾液酸酶活性(33.3%)和群落状态类型IV(CST IV)占优势(34.3%)的发生率显著更高(P<0.001)。多变量分析显示,pH值升高、Nugent评分≥7、过氧化氢产生阴性、CST IV、生物膜形成和高白细胞介素-6水平是HPV持续感染的独立预测因素。ROC分析表明,联合预测模型的曲线下面积(AUC)为0.842。Kaplan-Meier生存分析表明,阴道微生态正常的女性在24个月时的HPV清除率(90.1%)显著高于微生态失调的女性(66.2%,P<0.001)。此外,持续感染与肿瘤坏死因子-α升高、白细胞介素-12减少、C反应蛋白升高和氧化应激标志物有关。
阴道微生态失衡和免疫失调是HPV持续感染的主要决定因素。对这些因素进行综合评估可能会改善风险分层,并指导对HPV感染女性的个体化干预。