Vorsters Alex, Van Keer Severien, Biesmans Samantha, Hens Annick, De Coster Ilse, Goossens Herman, Ieven Margareta, Van Damme Pierre
Centre for the Evaluation of Vaccination, Vaccine & Infectious Disease Institute, University of Antwerp, 2610 Wilrijk, Belgium.
Laboratory of Medical Microbiology, Vaccine & Infectious Disease Institute, Faculty of Medicine and Health Sciences, University of Antwerp, 2610 Wilrijk, Belgium.
Int J Mol Sci. 2016 May 17;17(5):750. doi: 10.3390/ijms17050750.
The link between infection with high-risk human papillomavirus (hrHPV) and cervical cancer has been clearly demonstrated. Virological end-points showing the absence of persistent HPV infection are now accepted as a way of monitoring the impact of prophylactic vaccination programs and therapeutic vaccine trials. This study investigated the use of urine samples, which can be collected by self-sampling at home, instead of cervical samples for follow-up of an HPV intervention trial. Eighteen initially HPV DNA-positive women participating in an HPV therapeutic vaccine trial were monitored during a three-year follow-up period. A total of 172 urine samples and 85 cervical samples were collected. We obtained a paired urine sample for each of the 85 cervical samples by recovering urine samples from six monthly gynaecological examinations. We performed a small pilot study in which the participating women used a urine collection device at home and returned their urine sample to the laboratory by mail. All samples were analyzed using quantitative real-time HPV DNA PCR. A good association (κ value of 0.65) was found between the presence of HPV DNA in urine and a subsequent cervical sample. Comparisons of the number of HPV DNA copies in urine and paired cervical samples revealed a significant Spearman rho of 0.676. This correlation was superior in women with severe lesions. The HPV DNA results of the small pilot study based on self-collected urine samples at home are consistent with previous and subsequent urine and/or cervical results. We demonstrated that urine sampling may be a valid alternative to cervical samples for the follow-up of HPV intervention trials or programs. The potential clinical value of urine viral load monitoring should be further investigated.
高危型人乳头瘤病毒(hrHPV)感染与宫颈癌之间的联系已得到明确证实。目前,显示无持续性HPV感染的病毒学终点已被视为监测预防性疫苗接种计划和治疗性疫苗试验效果的一种方式。本研究调查了使用可在家自行采集的尿液样本替代宫颈样本,用于HPV干预试验随访的情况。在一项为期三年的随访期内,对18名最初HPV DNA呈阳性且参与HPV治疗性疫苗试验的女性进行了监测。共采集了172份尿液样本和85份宫颈样本。我们通过在每月一次的妇科检查中收集尿液样本,为85份宫颈样本中的每一份都获取了配对的尿液样本。我们开展了一项小型试点研究,参与研究的女性在家中使用尿液采集装置,然后通过邮寄将尿液样本送回实验室。所有样本均采用定量实时HPV DNA聚合酶链反应(PCR)进行分析。发现尿液中HPV DNA的存在与后续宫颈样本之间存在良好的相关性(κ值为0.65)。尿液和配对宫颈样本中HPV DNA拷贝数的比较显示,Spearman相关系数为0.676,具有显著性。这种相关性在患有严重病变的女性中更为明显。基于在家自行采集尿液样本的小型试点研究的HPV DNA结果与之前及后续的尿液和/或宫颈结果一致。我们证明,对于HPV干预试验或项目的随访,尿液采样可能是宫颈样本的有效替代方法。尿液病毒载量监测的潜在临床价值应进一步研究。