What is it about?

High-risk human papillomaviruses (HPVs) are highly prevalent worldwide, and HPV genotype distribution varies regionally. Molecular surveys of HPVs are important for effective HPV control and prevention. Fifteen high-risk HPV strains (16, 18, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 66, 68) and six low-risk HPV strains (HPV6, 11, 42, 43, 44, CP8304) were detected by cervical cytology from 10 501 subjects. High-risk HPVs, low-risk HPVs, and both high- and low-risk HPVs were detected in 14·5%, 2·8%, and 2·4% of cases, respectively. Of 1782 subjects with high-risk HPV infection, 75·5%, 18·1%, and 6·4% were infected with one, two, and 53 strains of high-risk HPVs, respectively. HPV52, HPV16, and HPV58 were the top three most dominant high-risk HPV genotypes in our population with positivity rates of 23·0%, 17·7% and 16·9%, respectively. Multiple infection was common, with significantly higher co-infection rates of HPV58/HPV33 (12·9%) and HPV58/HPV52 (11·3%). Further data comparisons showed that HPV genotype distribution varied markedly between domestic and international regions. In conclusion, a monolithic vaccination strategy is obviously impractical, and regional HPV surveillance is essential to optimize current HPV control and prevention.

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Why is it important?

The 3 most dominant HPV genotypes of our population were HPV52, HPV16, and HPV58. 24.5% of the HPV positive subjects were infected with two or more HPV strains. HPV58/HPV33 and HPV58/HPV52 showed significantly higher co-infection rates. HPV genotype distribution varied markedly between domestic and international regions. The complexity of HPV genotype distribution will reduce the efficiency of vaccines.

Perspectives

Our data will help to optimize current strategy for HPV control and prevention.

Professor Yu Zhang
the 7th People's Hospital of Shanghai

Read the Original

This page is a summary of: Genotype distribution characteristics of high-risk human papillomaviruses in women from Shanghai, China, Epidemiology and Infection, November 2015, Cambridge University Press,
DOI: 10.1017/s0950268815002721.
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