Journal of Clinical Virology
Volume 44, Issue 4 , Pages 314-317, April 2009

High level of HPV 16 and 18 DNA load in anal swabs from male and female HIV-1 infected patients

  • Isabelle Poizot-Martin

      Affiliations

    • Departement de Recherche Clinique CHU Sainte-Marguerite, Marseille, France
  • ,
  • Mireille Henry

      Affiliations

    • Fédération de Microbiologie Hospitalière, URMITE CNRS-IRD UMR 6236, CHU la Timone, France
  • ,
  • Serge Benhaim

      Affiliations

    • Departement de Recherche Clinique CHU Sainte-Marguerite, Marseille, France
  • ,
  • Véronique Obry-Roguet

      Affiliations

    • Departement de Recherche Clinique CHU Sainte-Marguerite, Marseille, France
  • ,
  • Dominique Figarella

      Affiliations

    • Laboratoire d’Anatomie-Pathologique, CHU la Timone, APHM, Marseille, France
  • ,
  • Catherine Tamalet

      Affiliations

    • Fédération de Microbiologie Hospitalière, URMITE CNRS-IRD UMR 6236, CHU la Timone, France
    • Corresponding Author InformationCorresponding author at: Laboratoire de Virologie Hôpital de la Timone, 264 Rue St Pierre, 13385 Marseille Cedex 05, France. Tel.: +33 4 91 38 55 22; fax: +33 4 91 38 55 18.

Received 10 September 2008; received in revised form 27 January 2009; accepted 4 February 2009. published online 09 March 2009.

Abstract 

Background

Despite HAART, the prevalence and incidence of anal cancer in HIV-infected individuals have increased. Recently, the relationship between the severity of cervical lesions and oncogenic HPV load was demonstrated; however, few studies have assessed the level and the significance of oncogenic HPV load in patients at risk for anal neoplasia.

Objectives

To assess HPV genotypes and HPV 16/18 DNA load in HIV-1 infected patients at risk for anal neoplasia.

Study design

Cross-sectional pilot study from male and female HIV-1 infected individuals at risk for anal neoplasia in an outpatient HIV Clinical Unit of Marseilles university Hospitals.

Results

Anal HPV was found in 79% of the patients whereas high-risk (HR) HPV types and infection with multiple HPV types were found in 83% and 61% of the patients, respectively. Using a sensitive real-time PCR, median HPV 16 and 18 DNA load were 5×106copies/106cells and 3.2×105copies/106cells, respectively. Notably, there were no significant differences in the HPV 16/18 viral loads with respect to the anoscopic results.

Conclusions

Longitudinal studies are needed to evaluate the link between high anal HPV DNA load and progression to anal squamous intraepithelial lesions and anal cancer.

Keywords: HPV load, HPV 16, HPV 18, Anal HPV infection

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PII: S1386-6532(09)00076-6

doi:10.1016/j.jcv.2009.02.003

Journal of Clinical Virology
Volume 44, Issue 4 , Pages 314-317, April 2009