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. 2007 Jul 12:2:15.
doi: 10.1186/1750-9378-2-15.

Progression and regression of incident cervical HPV 6, 11, 16 and 18 infections in young women

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Progression and regression of incident cervical HPV 6, 11, 16 and 18 infections in young women

Ralph P Insinga et al. Infect Agent Cancer. .

Abstract

Background: We describe type-specific progression, regression and persistence of incident human papillomavirus (HPV)-6-11-16 and -18 infections, along with type distribution in cervical intra-epithelial neoplasia (CIN) lesions.

Methods: The study population consisted of 16-23 year-old women undergoing Pap testing and cervical swab polymerase chain reaction testing for HPV DNA at approximate 6 month intervals for up to 4 years in the placebo arm of a clinical trial of an HPV 16-vaccine. HPV types in incident infections were correlated with types in lesion biopsy specimens.

Results: 56.7% of CIN-1 and nearly one-third of CIN-2/3 lesions following incident HPV-6-11-16 or -18 infections did not correlate with the incident infection HPV type. Cumulative 36-month progression rates to CIN-2/3 testing positive for the relevant HPV type were highest for HPV-16 infections (16.5%), followed by HPV-18 (8.2%). Overall, 26.0% of CIN-1, 50.0% of CIN-2 and 70.6% of CIN-3 biopsies tested positive for HPV-6-11-16-18 infections.

Conclusion: Women with a given HPV type may often be co-infected or subsequently infected with other types which may lead to subsequent cervical lesions. This issue has been addressed in this study reporting data for the natural history of HPV-6-11-16 and -18 infections and is a relevant consideration in designing future studies to evaluate the incidence/risk of CIN following other type-specific HPV infections.

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Figures

Figure 1
Figure 1
Sample selection criteria for analyses of incident HPV 6, 11, 16 and 18 infections. The final samples of women with incident HPV infections eligible for each type-specific analysis are represented within the bottom box, labeled by HPV type. These were comprised of placebo arm women with incident type-specific infections who were negative on PCR testing for the relevant HPV type on the first two trial endo/ecto-cervical swabs and any intervening cervical biopsies.

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