Department of Laboratory Medicine, Skåne University Hospital, Lund University, Malmö, Sweden.
Departments of Laboratory Medicine, Medical Epidemiology & Biostatistics, Karolinska Institutet and Departments of Clinical Microbiology and Pathology, Karolinska Hospital, Stockholm, Sweden.
J Gen Virol. 2013 May;94(Pt 5):1096-1103. doi: 10.1099/vir.0.048561-0. Epub 2013 Jan 23.
Whereas the antibody response to the anogenital human papillomaviruses (HPVs) is known to be mainly type-specific, correlated with the presence of viral DNA and mainly directed to conformational epitopes of the virion, it is not known if this applies also to the antibody response to cutaneous HPVs. For 434 non-immunosuppressed patients with skin lesions (squamous cell carcinoma and basal cell carcinoma of the skin, actinic keratosis and benign skin lesions), we compared HPV DNA status with seroreactivity to HPV pseudovirions (PsV) and to GST-L1 fusion proteins from HPV types -5, -6, -15, -16, -32 and -38. Biopsies from the skin lesions were tested for the presence of HPV DNA using three different PCR methods, with typing by sequencing. Serum samples from subjects with HPV DNA-positive biopsies and randomly selected serum samples from subjects with HPV DNA-negative biopsies were also tested with neutralization assays with HPV5, -38 and -76 PsV. Agreement of the three serological methods varied from poor to moderate. Type-specific seroprevalences among patients positive for the same type of HPV DNA (sensitivity of serology) was improved with the PsV-based method (mean of 40%, maximum 63%) compared with the GST-L1 method (mean of 20%, maximum of 25%). Neutralization was the most sensitive assay for HPV38 (50%). In summary, cutaneous HPVs also appear to induce a type-specific antibody response that correlates with the presence of HPV DNA and that can be detected with improved sensitivity using PsV-based serology.
虽然已知针对肛门生殖器人乳头瘤病毒(HPV)的抗体反应主要是针对特定类型的,与病毒 DNA 的存在相关,并主要针对病毒粒子的构象表位,但尚不清楚这是否也适用于针对皮肤 HPV 的抗体反应。我们对 434 名非免疫抑制的皮肤病变患者(皮肤鳞状细胞癌和基底细胞癌、光化性角化病和良性皮肤病变)进行了比较,将 HPV DNA 状态与 HPV 假病毒(PsV)和 HPV 类型的 GST-L1 融合蛋白的血清反应性进行了比较-5、-6、-15、-16、-32 和 -38。使用三种不同的 PCR 方法和测序进行 HPV DNA 检测,对皮肤病变活检进行 HPV DNA 检测。对 HPV DNA 阳性活检的受试者的血清样本和 HPV DNA 阴性活检的随机选择的血清样本也用 HPV5、-38 和 -76 PsV 的中和测定进行了测试。三种血清学方法的一致性从差到中等不等。对于 HPV DNA 相同类型阳性的患者(血清学的敏感性),基于 PsV 的方法(平均 40%,最高 63%)比 GST-L1 方法(平均 20%,最高 25%)提高了针对 HPV 的特定血清阳性率。中和是针对 HPV38 最敏感的检测方法(50%)。综上所述,皮肤 HPV 似乎也会引起与 HPV DNA 存在相关的针对特定类型的抗体反应,并且使用基于 PsV 的血清学可以提高其敏感性来检测。