Huang Jun, Yin Cunsi, Wang Junli
Department of Gynaecology, Maanshan Maternal and Child Health Care Hospital, Ma'anshan, Anhui, China.
J Obstet Gynaecol. 2023 Dec;43(1):2161349. doi: 10.1080/01443615.2022.2161349.
High-risk (HR)-human papillomavirus (HPV) is the leading cause of precancerous cervical lesions in patients with chronic untreated infection. We investigated the relationships among several vaginal microbiological alterations, oncogene E6/E7 expression, and HR-HPV. A total of 1327 women who underwent HPV screening, vaginal microecology determination, and fluid-based thin-layer cytological test were enrolled and classified into the HPV-negative group, the low-risk (LR)-HPV-positive group, and the HR-HPV-positive group. The status of cervical HPV infection, vaginal microecology, and E6/E7 mRNA expression were examined sequentially. The effect of HR-HPV infection on cervical cancer (CC) was meticulously assessed, and associations between HR-HPV infection and vaginal microecology and E6/E7 mRNA were identified. In total 548/1327 patients were HPV positive, including LR-HPV infection ( = 132) and HR-HPV infection ( = 416). Patients in the HR-HPV positive group revealed higher detection rates of bacterial vaginosis (BV), trichomonal vaginitis (TV), and vulvovaginal candidiasis (VVC) relative to the HPV negative group. A higher E6/E7 mRNA expression was identified in HR-HPV patients compared to LR-HPV patients. BV and E6/E7 mRNA were classified as independent risk factors for HR-HPV infection. Patients with HR-HPV infection were more susceptible to CC development. Overall, BV and E6/E7 mRNA expression were identified as independent risk factors for HR-HPV infection.IMPACT STATEMENT Through literature review, we found that vaginal ecological changes increase the risk of HPV infection, and HPV persistent infection is an important risk factor for cervical precancerous lesions and cervical cancer. In addition, HPV gene E6/E7 is expressed in HPV-positive cervical cancer cells, which is related to cell malignant transformation and even tumorigenesis. This study further revealed that bacterial vaginosis (BV) and E6/E7 mRNA were independently correlated with HR-HPV infection, and HR-HPV infection increased the risk of cervical cancer. E6/E7 mRNA detection may be used as a new auxiliary diagnostic index for HR-HPV infection. In addition, this study provides a reference for whether the restoration of vaginal microecological balance in patients with BV undergoing clinical treatment is conducive to HR-HPV regression, and provides theoretical support for the prevention and control of cervical cancer microecological approach and the occurrence and development of cervical cancer.
高危(HR)-人乳头瘤病毒(HPV)是慢性未治疗感染患者宫颈癌前病变的主要原因。我们研究了几种阴道微生物改变、癌基因E6/E7表达和HR-HPV之间的关系。共有1327名接受HPV筛查、阴道微生态测定和液基薄层细胞学检查的女性被纳入研究,并分为HPV阴性组、低危(LR)-HPV阳性组和HR-HPV阳性组。依次检查宫颈HPV感染状况、阴道微生态和E6/E7 mRNA表达。仔细评估HR-HPV感染对宫颈癌(CC)的影响,并确定HR-HPV感染与阴道微生态和E6/E7 mRNA之间的关联。总共548/1327例患者HPV阳性,包括LR-HPV感染(n = 132)和HR-HPV感染(n = 416)。与HPV阴性组相比,HR-HPV阳性组患者细菌性阴道病(BV)、滴虫性阴道炎(TV)和外阴阴道假丝酵母菌病(VVC)的检出率更高。与LR-HPV患者相比,HR-HPV患者中E6/E7 mRNA表达更高。BV和E6/E7 mRNA被归类为HR-HPV感染的独立危险因素。HR-HPV感染患者更易发生CC。总体而言,BV和E6/E7 mRNA表达被确定为HR-HPV感染的独立危险因素。影响声明 通过文献回顾,我们发现阴道生态变化会增加HPV感染风险,而HPV持续感染是宫颈前病变和宫颈癌的重要危险因素。此外,HPV基因E6/E7在HPV阳性宫颈癌细胞中表达,这与细胞恶性转化甚至肿瘤发生有关。本研究进一步揭示,细菌性阴道病(BV)和E6/E7 mRNA与HR-HPV感染独立相关,且HR-HPV感染会增加宫颈癌风险。E6/E7 mRNA检测可作为HR-HPV感染的一项新的辅助诊断指标。此外,本研究为临床治疗的BV患者恢复阴道微生态平衡是否有利于HR-HPV消退提供参考,为宫颈癌微生态防治方法及宫颈癌发生发展提供理论支持。