WHO HPV LabNet Global Reference Laboratory, Department of Clinical and Medical Microbiology, Laboratory Medicine Skåne, and Lund University, Malmö, Sweden.
J Clin Microbiol. 2012 Jul;50(7):2289-98. doi: 10.1128/JCM.00840-12. Epub 2012 Apr 25.
Accurate and internationally comparable human papillomavirus (HPV) DNA genotyping is essential both for evaluation of HPV vaccines and for effective monitoring and implementation of vaccination programs. The World Health Organization (WHO) HPV Laboratory Network (LabNet) regularly issues international proficiency studies. The 2010 HPV genotyping proficiency panel for HPV vaccinology contained 43 coded samples composed of purified plasmids of 16 HPV types (HPV types 6, 11, 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68a and 68b) and 3 coded extraction controls. Proficient typing was defined as detection in both single and multiple infections of 50 international units (IU) of HPV type 16 (HPV-16) and HPV-18 DNA and 500 genome equivalents (GE) for the other 14 HPV types. Ninety-eight laboratories worldwide submitted a total of 132 data sets. Twenty-four different HPV genotyping assay methods were used, with Linear Array being the most commonly used. Other major assays used were a line blot assay (Inno-LiPa), CLART, type-specific real-time PCR, PCR Luminex, and different microarray assays. Altogether, 72 data sets were proficient for detection of more than 1 type, and only 26 data sets proficiently detected all 16 HPV types. The major oncogenic HPV types, 16 and 18, were proficiently detected in 95.0% (114/120) and 87.0% (94/108) of data sets, respectively. Forty-six data sets reported multiple false-positive results and were considered nonproficient. A trend toward increased sensitivity of assays was seen for the 41 laboratories that participated in both 2008 and 2010. In conclusion, continued global proficiency studies will be required for establishing comparable and reliable HPV genotyping services for vaccinology worldwide.
准确且具有国际可比性的人乳头瘤病毒 (HPV) DNA 基因分型对于 HPV 疫苗的评估以及有效监测和实施疫苗接种计划至关重要。世界卫生组织 (WHO) HPV 实验室网络 (LabNet) 定期发布国际能力研究。2010 年 HPV 基因分型能力研究面板包含 43 个编码样本,由 16 种 HPV 类型(HPV 类型 6、11、16、18、31、33、35、39、45、51、52、56、58、59、66 和 68a 和 68b)的纯化质粒组成,以及 3 个编码提取对照。熟练的分型定义为在 50 国际单位 (IU) HPV 类型 16 (HPV-16) 和 HPV-18 DNA 的单一和多重感染以及其他 14 种 HPV 类型的 500 个基因组当量 (GE) 中进行检测。全球 98 家实验室共提交了 132 组数据。使用了 24 种不同的 HPV 基因分型检测方法,其中线性阵列法最为常用。使用的其他主要检测方法是线印迹检测法 (Inno-LiPa)、CLART、型特异性实时 PCR、PCR Luminex 和不同的微阵列检测法。总共,72 个数据集能够检测超过 1 种类型,只有 26 个数据集能够熟练地检测所有 16 种 HPV 类型。主要的致癌 HPV 类型 16 和 18 在 95.0%(114/120)和 87.0%(94/108)的数据集分别得到熟练检测。46 个数据集报告了多个假阳性结果,被认为是不熟练的。在参加 2008 年和 2010 年两次的 41 个实验室中,检测方法的敏感性呈上升趋势。总之,需要继续进行全球能力研究,以便为全球疫苗接种建立可比和可靠的 HPV 基因分型服务。