Department of Population Health, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Department of Population Health, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
J Clin Virol. 2018 Apr;101:34-37. doi: 10.1016/j.jcv.2018.01.013. Epub 2018 Jan 31.
Several new members of the human polyomavirus (HPyV) family that infect human skin and are potentially oncogenic have been identified in the last decade.
To investigate prospectively the seroprevalence and stability of 13 PyVs, and possible associations with different risk factors and cutaneous squamous cell carcinoma (cSCC).
In this Australian population-based longitudinal study sera were collected at baseline in 1992 or during the next 4 years from 688 people. Of the 688, 226 developed a new cSCC between blood collection and the final follow up in 2003. The remaining 462 served as controls. Among the 462 controls, 161 had a second serum sample from 2003 analysed. Seroprevalence of 10 human PyVs (BKV, JCV, KIV, WUV, MCV, TSV, HPyV6, HPyV7, HPyV9 and HPyV10) and three non-human PyVs (SV40, LPV and ChPyV) was assessed using multiplex serology.
There was no significant difference in PyV seroprevalence between people who developed cSCC during follow-up compared to those who did not. WUV and HPyV10 showed the highest serostability (93%) and JCV VP1 and SV40 VP1 the lowest (84%) over a 9-year time period (range 7-11 years).
We found no evidence that HPyV seroprevalence is associated with subsequent development of cSCC and observed variable stability of antibodies to polyomaviruses.
在过去十年中,已经鉴定出了几种感染人类皮肤且具有潜在致癌性的新型人类多瘤病毒(HPyV)家族成员。
前瞻性研究 13 种多瘤病毒的血清流行率和稳定性,以及与不同危险因素和皮肤鳞状细胞癌(cSCC)的可能关联。
在这项澳大利亚基于人群的纵向研究中,1992 年或接下来的 4 年内从 688 人采集了基线血清。在这 688 人中,有 226 人在采血和 2003 年最终随访之间发生了新的 cSCC。其余 462 人作为对照组。在这 462 名对照者中,有 161 人在 2003 年进行了第二次血清样本分析。使用多重血清学方法评估了 10 种人类多瘤病毒(BKV、JCV、KIV、WUV、MCV、TSV、HPyV6、HPyV7、HPyV9 和 HPyV10)和 3 种非人类多瘤病毒(SV40、LPV 和 ChPyV)的血清流行率。
在随访期间发生 cSCC 的人与未发生 cSCC 的人之间,多瘤病毒血清流行率没有显著差异。在 9 年时间内(7-11 年),WUV 和 HPyV10 的血清阳性率最高(93%),JCV VP1 和 SV40 VP1 的血清阳性率最低(84%)。
我们没有发现 HPyV 血清流行率与随后发生的 cSCC 之间存在关联的证据,并且观察到多瘤病毒抗体的稳定性存在差异。