The prevalence of human leucocyte antigen and human papillomavirus DNA in penile intraepithelial neoplasia in England 2011–2012

Author:

Shim Tang Ngee1ORCID,Harwood Catherine A2,Marsh Steven GE3,Gotch Frances M4,Quint Wim5,de Koning Maurits N5,Francis Nick6,Jameson Charles7,Freeman Alex7,Minhas Suks8,Muneer Asif8,Dinneen Michael9,Bunker Christopher B1

Affiliation:

1. Dermatology Department, University College Hospital, Chelsea and Westminster Hospital, London, UK

2. Center for Cutaneous Research and Cell Biology, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK

3. Anthony Nolan Research Institute and University College London Cancer Institute, London, UK

4. Immunology Department, Imperial College, London, UK

5. DDL Diagnostic Laboratory, Rijswijk, Netherlands

6. Pathology Department, Imperial College Healthcare NHS Trust, London, UK

7. Pathology Department, University College London Hospital, London, UK

8. Andrology Centre and the Institute of Urology, University College London Hospital, London, UK

9. Urology Department, Chelsea and Westminster Hospital, London, UK

Abstract

Background: The pathogenesis of penile intraepithelial neoplasia (PeIN) is unclear but human papillomavirus (HPV) infection and polymorphisms in human leucocyte antigen (HLA). Objectives: To examine the prevalence of HPV DNA and HLA in PeIN. Methods: Adult Caucasian men with a clinical and histological diagnosis of PeIN, that is, Bowenoid papulosis (BP), Bowen’s disease of penis (BDP) and erythroplasia of Queyrat (EQ) were selected and phenotyped from the clinical records. DNA was extracted from blood and paraffin-embedded sections for HLA and HPV typing, respectively. Human leucocyte antigen allele frequencies were compared with those derived from the UK–based Caucasian population. Results: Seventy-two cases of PeIN (20 BP, 34 BDP and 18 EQ) were studied. Human papillomavirus DNA was identified in 65/72 (90.2%) PeIN; Alphapapillomavirus types were detected in 62/72 (85%) followed by Betapapillomavirus types in 9/72 (12.5%) and cutaneous types in 7/72 (9.7%); HPV16 was the most prevalent genotype at 35/72 (48.6%) followed by HPV33 at 7/72 (9.7%); multiple infections were seen in 18/72 (25%) PeIN. HLA-C*15 (Bonferroni corrected p = 0.049) confers susceptibility to PeIN, whereas HLA-DQA1*01 (corrected p = 0.02) protects against PeIN. HPV16-associated PeIN cases showed no statistically significant association with HLA genotype after multiple corrections. Conclusion: Human papillomavirus is involved in the pathogenesis of PeIN. Immunogenotype may play a role in the pathogenesis of PeIN.

Funder

Skin Treatment and Research Trust

Sir John Fisher Foundation

Publisher

SAGE Publications

Subject

Infectious Diseases,Pharmacology (medical),Public Health, Environmental and Occupational Health,Dermatology

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