UBRISA

View Item 
  •   Ubrisa Home
  • Faculty of Medicine
  • Obstetrics & Gynaecology
  • Research articles (Dept of Obstetrics & Gynaecology)
  • View Item
  •   Ubrisa Home
  • Faculty of Medicine
  • Obstetrics & Gynaecology
  • Research articles (Dept of Obstetrics & Gynaecology)
  • View Item
    • Login
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Co-infection with HPV types from the same species provides natural cross-protection from progression to cervical cancer

    Thumbnail
    View/Open
    Sobota et al (2014) Co-infection with HPV types from the same species.pdf (251.9Kb)
    Date
    2014-08
    Author
    Sobota, Rafal S.
    Ramogola-Masire, Doreen
    Williams, Scott M.
    Zetola, Nicola M.
    Publisher
    BioMed Central (BMC), http://www.infectagentscancer.com/
    Link
    http://www.infectagentscancer.com/content/9/1/26
    Rights
    Distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
    Rights holder
    Authors
    Type
    Published Article
    Metadata
    Show full item record
    Abstract
    Background: The worldwide administration of bivalent and quadrivalent HPV vaccines has resulted in cross-protection against non-vaccine HPV types. Infection with multiple HPV types may offer similar cross-protection in the natural setting. We hypothesized that infections with two or more HPV types from the same species, and independently, infections with two or more HPV types from different species, associate with protection from high-grade lesions. Findings: We recruited a cohort of 94 HIV, HPV-positive women from Botswana, with Grade 2 or higher cervical intraepithelial neoplasia. Infections with 2 or more HPV types from a single species associated with reduced lesion severity in univariate analysis (OR = 0.41, 95% CI 0.18-0.97, p = 0.042), when adjusted for the presence of HPV 16 or 18 types (OR = 0.41, 95% CI 0.17-1.00, p = 0.049), or all high-risk HPV type infections (OR = 0.38, 95% CI 0.16-0.90, p = 0.028). Infections with 2 or more HPV types from different species did not associate (OR = 0.68, 95% CI 0.25-1.81, p = 0.435). Conclusions: Our findings show that co-infections with genetically similar HPV types reduce the likelihood of progression to high-grade lesions in HIV positive women, an effect not observed in co-infections with taxonomically different HPV types. This observation is possibly caused by an immune cross-protection through a similar mechanism to that observed after HPV vaccination.
    URI
    http://hdl.handle.net/10311/2174
    Collections
    • Research articles (Dept of Obstetrics & Gynaecology) [14]

    DSpace software copyright © 2002-2015  DuraSpace
    Contact Us | Send Feedback
    Theme by 
    @mire NV
     

     

    Browse

    All of UBRISA > Communities & Collections > By Issue Date > Authors > Titles > SubjectsThis Collection > By Issue Date > Authors > Titles > Subjects

    My Account

    > Login > Register

    Statistics

    > Most Popular Items > Statistics by Country > Most Popular Authors