Frequency and clinical significance of human β-herpesviruses in cervical samples from Italian women
Human papillomaviruses (HPVs) are necessary, but not sufficient, for the development of cervical cancer (CC). Human β-herpesviruses (β-HHVs) have been suggested as possible cofactors in the oncogenesis of CC. In this cross-sectional study, the prevalence and possible association of cytomegalovirus (...
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Veröffentlicht in: | Journal of medical virology 2008, Vol.80 (1), p.147-153 |
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Zusammenfassung: | Human papillomaviruses (HPVs) are necessary, but not sufficient, for the development of cervical cancer (CC). Human β-herpesviruses (β-HHVs) have been suggested as possible cofactors in the oncogenesis of CC. In this cross-sectional study, the prevalence and possible association of cytomegalovirus (CMV), HHV-6 and -7 with HPV presence was investigated by quantitative real-time PCR assays in cervical samples obtained from 208 italian women. The two most common high-risk HPV types found were 31 and 16. Overall, the positive rates for CMV, HHV-6 and HHV-7 were 66%, 25%, and 6%, respectively. In particular, the prevalence of CMV was found to be extremely high irrespective of either the cytological category or HPV positivity. The prevalence of HHV-6 DNA was significantly higher in high-grade squamous intraepithelial lesions (HSIL) respect to normal women (P < 0.017); by contrast, the prevalence HHV-7 DNA was generally low and not associated with SIL. Copresence of CMV and HHV-6 DNA was found to be significantly higher in patients with SIL respect to normal women (P < 0.05). No correlation was demonstrated between the viral load of all three β-HHVs and the different cytological stages or with the HPV presence. A few patients with severe disease however showed very high viral loads which for HHV-6 may be indicative of viral integration. In conclusion, this study suggests that CMV and HHV-7 alone are probably not implicated in the oncogenesis of CC whilst HHV-6 alone or together with CMV may contribute to the development of CC. J. Med. Virol. 80:147-153, 2008. © 2007 Wiley-Liss, Inc. |
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ISSN: | 0146-6615 1096-9071 |
DOI: | 10.1002/jmv.21054 |