Prevalence and stability of antibodies to thirteen polyomaviruses and association with cutaneous squamous cell carcinoma: A population-based study

被引:7
作者
Antonsson, Annika [1 ]
Neale, Rachel E. [1 ]
O'Rourke, Peter [1 ]
Wockner, Leesa [1 ]
Michel, Angelika [2 ]
Pawlita, Michael [2 ]
Waterboer, Tim [2 ]
Green, Adele C. [1 ,3 ,4 ]
机构
[1] QIMR Berghofer Med Res Inst, Dept Populat Hlth, Brisbane, Qld, Australia
[2] German Canc Res Ctr, Deutsch Krebsforschungszentrum, DKFZ, Mol Diagnost Oncogen Infect Div, Heidelberg, Germany
[3] CRUK Manchester Inst, Manchester, Lancs, England
[4] Univ Manchester, Manchester Acad Hlth Sci Ctr, Manchester, Lancs, England
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
Polyomavirus; Serology; Cutaneous squamous cell carcinoma; GLUTATHIONE-S-TRANSFERASE; SKIN-CANCER; PROTEINS; SEROLOGY;
D O I
10.1016/j.jcv.2018.01.013
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Several new members of the human polyomavirus (HPyV) family that infect human skin and are potentially oncogenic have been identified in the last decade. Objectives: To investigate prospectively the seroprevalence and stability of 13 PyVs, and possible associations with different risk factors and cutaneous squamous cell carcinoma (cSCC). Study design: 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. Results: 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). Conclusions: We found no evidence that HPyV seroprevalence is associated with subsequent development of cSCC and observed variable stability of antibodies to polyomaviruses.
引用
收藏
页码:34 / 37
页数:4
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