TY - JOUR
T1 - Prevalence and stability of antibodies to thirteen polyomaviruses and association with cutaneous squamous cell carcinoma
T2 - A population-based study
AU - Antonsson, Annika
AU - Neale, Rachel E.
AU - O'Rourke, Peter
AU - Wockner, Leesa
AU - Michel, Angelika
AU - Pawlita, Michael
AU - Waterboer, Tim
AU - Green, Adèle C.
PY - 2018/4/1
Y1 - 2018/4/1
N2 - 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.
AB - 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.
KW - Cutaneous squamous cell carcinoma
KW - Polyomavirus
KW - Serology
UR - http://www.scopus.com/inward/record.url?scp=85041391123&partnerID=8YFLogxK
U2 - 10.1016/j.jcv.2018.01.013
DO - 10.1016/j.jcv.2018.01.013
M3 - Article
AN - SCOPUS:85041391123
SN - 1386-6532
VL - 101
SP - 34
EP - 37
JO - Journal of Clinical Virology
JF - Journal of Clinical Virology
ER -