Proyecto Epidemiológico Guanacaste, Fundación INCIENSA, Guanacaste, Costa Rica.
J Clin Microbiol. 2012 Dec;50(12):3870-6. doi: 10.1128/JCM.01698-12. Epub 2012 Sep 19.
Liquid-based methods for the collection, transportation, and storage of cervical cells are cumbersome and expensive and involve laborious DNA extraction. An FTA cartridge is a solid carrier device, easier to handle and allowing simple DNA elution for human papillomavirus (HPV) testing. HPV-DNA results from cervical specimens collected in PreservCyt medium (Hologic, Inc.) and the indicating FTA elute cartridge were compared in an area where transportation and storage may affect the performance of the test. Cervical cells from 319 young adult women enrolled in the Costa Rica Vaccine Trial were collected by a nurse using a Cervex brush (Roberts), which was placed on the FTA cartridge and subsequently rinsed in 20 ml of PreservCyt medium. Two 0.5-ml PreservCyt aliquots were frozen for HPV-PCR testing; the FTA cartridges were kept at room temperature. HPV-DNA detection and typing was performed using SPF(10) PCR/DEIA (DNA enzyme immunoassay detection of amplimers)/LiPA(25) system. The percent agreement, agreement among positives, and kappas were estimated. Positivity was higher for FTA compared to PreservCyt specimens (54.5% versus 45.8%, P < 0.001). For oncogenic types, the overall agreement was 0.92, the agreement between positives was 0.74, and the kappa was 0.79. For individual HPV types, the overall agreement ranged from 0.97 to 1.00. We did not observe reduced cytology adequacy when specimen collection for cytology was preceded by FTA collection for HPV testing. HPV-DNA detection from FTA cartridges is broadly comparable to detection from PC medium. The higher HPV detection observed for FTA-collected specimens should be explored further. FTA cartridges could provide a simpler and more cost-effective method for cervical cell collection, storage, and transportation for HPV-DNA detection in research settings in developing countries.
液基方法用于收集、运输和储存宫颈细胞既繁琐又昂贵,并且涉及到繁琐的 DNA 提取。FTA 卡是一种固体载体设备,更易于操作,并允许简单地洗脱 DNA 进行人乳头瘤病毒 (HPV) 检测。在可能影响测试性能的地区,比较了用 PreservCyt 介质(Hologic,Inc.)收集的宫颈标本和指示 FTA 洗脱卡上的 HPV-DNA 结果。来自哥斯达黎加疫苗试验中 319 名年轻成年女性的宫颈细胞由护士使用 Cervx 刷子(Roberts)收集,将刷子放在 FTA 卡上,然后用 20ml PreservCyt 介质冲洗。两个 0.5ml PreservCyt 等分试样被冷冻用于 HPV-PCR 检测;FTA 卡保存在室温下。使用 SPF(10)PCR/DEIA(扩增子的 DNA 酶免疫测定检测)/LiPA(25)系统进行 HPV-DNA 检测和分型。估计了百分比一致性、阳性一致性和 Kappa 值。与 PreservCyt 标本相比,FTA 标本的阳性率更高(54.5%对 45.8%,P<0.001)。对于致癌型,总一致性为 0.92,阳性之间的一致性为 0.74,Kappa 值为 0.79。对于个体 HPV 型,总一致性范围为 0.97 至 1.00。当 HPV 检测前先用 FTA 收集标本进行细胞学检测时,并未观察到细胞学充分性降低。从 FTA 卡上检测 HPV-DNA 与从 PC 介质上检测 HPV-DNA 基本相当。对于 FTA 收集的标本观察到的更高 HPV 检测率需要进一步探索。FTA 卡可提供一种更简单、更具成本效益的方法,用于发展中国家研究环境中 HPV-DNA 的宫颈细胞收集、储存和运输。