Albrecht Valérie, Chevallier Anne, Magnone Virginie, Barbry Pascal, Vandenbos Fanny, Bongain André, Lefebvre Jean-Claude, Giordanengo Valérie
Laboratoire de Virologie, Hôpital de l'Archet, BP 3079, 151 route de Saint-Antoine de Ginestière, 06200 Nice Cedex 3, France.
J Virol Methods. 2006 Nov;137(2):236-44. doi: 10.1016/j.jviromet.2006.06.023. Epub 2006 Aug 1.
Persistent cervical high-risk human papillomavirus (HPV) infection is correlated with an increased risk of developing a high-grade cervical intraepithelial lesion. A two-step method was developed for detection and genotyping of high-risk HPV. DNA was firstly amplified by asymmetrical PCR in the presence of Cy3-labelled primers and dUTP. Labelled DNA was then genotyped using DNA microarray hybridization. The current study evaluated the technical efficacy of laboratory-designed HPV DNA microarrays for high-risk HPV genotyping on 57 malignant and non-malignant cervical smears. The approach was evaluated for a broad range of cytological samples: high-grade squamous intraepithelial lesions (HSIL), low-grade squamous intraepithelial lesions (LSIL) and atypical squamous cells of high-grade (ASC-H). High-risk HPV was also detected in six atypical squamous cells of undetermined significance (ASC-US) samples; among them only one cervical specimen was found uninfected, associated with no histological lesion. The HPV oligonucleotide DNA microarray genotyping detected 36 infections with a single high-risk HPV type and 5 multiple infections with several high-risk types. Taken together, these results demonstrate the sensitivity and specificity of the HPV DNA microarray approach. This approach could improve clinical management of patients with cervical cytological abnormalities.
持续性宫颈高危型人乳头瘤病毒(HPV)感染与高级别宫颈上皮内瘤变风险增加相关。开发了一种用于检测高危型HPV并进行基因分型的两步法。首先在存在Cy3标记引物和dUTP的情况下通过不对称PCR扩增DNA。然后使用DNA微阵列杂交对标记的DNA进行基因分型。本研究评估了实验室设计的HPV DNA微阵列对57份恶性和非恶性宫颈涂片进行高危型HPV基因分型的技术效果。该方法针对广泛的细胞学样本进行了评估:高级别鳞状上皮内病变(HSIL)、低级别鳞状上皮内病变(LSIL)和高级别非典型鳞状细胞(ASC-H)。在6份意义不明确的非典型鳞状细胞(ASC-US)样本中也检测到了高危型HPV;其中仅发现1份宫颈标本未感染,且无组织学病变。HPV寡核苷酸DNA微阵列基因分型检测到36例单一高危型HPV感染和5例多种高危型HPV混合感染。综上所述,这些结果证明了HPV DNA微阵列方法的敏感性和特异性。该方法可改善宫颈细胞学异常患者的临床管理。