Cuschieri K S, Cubie H A, Whitley M W, Seagar A L, Arends M J, Moore C, Gilkisson G, McGoogan E
Royal Infirmary of Edinburgh, 51 Little France Crescent, Edinburgh EH16 4SA, UK.
J Clin Pathol. 2004 Jan;57(1):68-72. doi: 10.1136/jcp.57.1.68.
If human papillomavirus (HPV) testing is to be included within cervical screening programmes, the importance of multiple HPV infections in cervical neoplasia needs to be determined. This study investigated the diversity of multiple HPV types in a routine cervical screening population, and assessed associations with cervical neoplasia.
Overall HPV prevalence, type specific prevalence, and extent of multiple infection were assessed in residual material from 3444 liquid based cytology samples, using real time GP5+/GP6+ polymerase chain reaction for screening and linear array assay for genotyping. HPV status was studied in relation to age and concurrent cytological evidence of dyskaryosis.
Twenty per cent of samples were HPV positive. HPV type diversity was broad, and multiple HPV infections occurred in half of the HPV positive samples. Younger women were significantly more likely to harbour multiple high risk HPV (HR-HPV) infections. Infections with multiple HR-HPV types were found in 3.4% of samples negative for neoplasia and in 33.3%, 41.8%, and 40.4% of samples with borderline, mild, or high grade dyskaryosis, respectively. Single HR-HPV infections were found in 4.9%, 38.6%, 45.0%, and 51.1% of negative, borderline, mild, or high grade dyskaryosis samples, respectively.
Multiple HR-HPV infections were most prevalent in young women. Multiple HR-HPV infections were not more frequent in high grade than in low grade cervical neoplasia, reflecting common sexual transmission of multiple HR-HPV. Prospective cohort studies linking sequential loss or gain of HPV types with cytological analysis are required to assess the impact of multiple HR-HPV infections on neoplastic progression.
若要将人乳头瘤病毒(HPV)检测纳入宫颈癌筛查项目,需确定多重HPV感染在宫颈肿瘤形成中的重要性。本研究调查了常规宫颈癌筛查人群中多种HPV类型的多样性,并评估了其与宫颈肿瘤形成的相关性。
使用实时GP5+/GP6+聚合酶链反应进行筛查,线性阵列分析进行基因分型,对3444份液基细胞学样本的剩余材料评估总体HPV患病率、型特异性患病率和多重感染程度。研究HPV状态与年龄及同时存在的细胞异型性细胞学证据的关系。
20%的样本HPV呈阳性。HPV类型多样性广泛,一半的HPV阳性样本存在多重HPV感染。年轻女性感染多种高危HPV(HR-HPV)的可能性显著更高。在肿瘤阴性样本中,3.4%的样本发现感染多种HR-HPV类型,而在存在临界、轻度或高度细胞异型性的样本中,这一比例分别为33.3%、41.8%和40.4%。在肿瘤阴性、临界、轻度或高度细胞异型性样本中,分别有4.9%、38.6%、45.0%和51.1%的样本发现单一HR-HPV感染。
多重HR-HPV感染在年轻女性中最为普遍。在高级别宫颈肿瘤中,多重HR-HPV感染并不比低级别宫颈肿瘤更常见,这反映了多种HR-HPV常见的性传播途径。需要进行前瞻性队列研究,将HPV类型的相继丢失或获得与细胞学分析联系起来,以评估多重HR-HPV感染对肿瘤进展的影响。