Human Papillomavirus Oral- and Sero- Positivity in Fanconi Anemia

Author:

Sauter Sharon L.ORCID,Zhang Xue,Romick-Rosendale Lindsey,Wells Susanne I.,Myers Kasiani C.,Brusadelli Marion G.,Poff Charles B.,Brown Darron R.,Panicker Gitika,Unger Elizabeth R.ORCID,Mehta Parinda A.,Bleesing Jack,Davies Stella M.,Butsch Kovacic Melinda

Abstract

High-risk human papillomavirus (HPV) is prevalent and known to cause 5% of all cancers worldwide. The rare, cancer prone Fanconi anemia (FA) population is characterized by a predisposition to both head and neck squamous cell carcinomas and gynecological cancers, but the role of HPV in these cancers remains unclear. Prompted by a patient-family advocacy organization, oral HPV and HPV serological studies were simultaneously undertaken. Oral DNA samples from 201 individuals with FA, 303 unaffected family members, and 107 unrelated controls were tested for 37 HPV types. Serum samples from 115 individuals with FA and 55 unrelated controls were tested for antibodies against 9 HPV types. Oral HPV prevalence was higher for individuals with FA (20%) versus their parents (13%; p = 0.07), siblings (8%, p = 0.01), and unrelated controls (6%, p ≤ 0.001). A FA diagnosis increased HPV positivity 4.84-fold (95% CI: 1.96–11.93) in adjusted models compared to unrelated controls. Common risk factors associated with HPV in the general population did not predict oral positivity in FA, unlike unrelated controls. Seropositivity and anti-HPV titers did not significantly differ in FA versus unrelated controls regardless of HPV vaccination status. We conclude that individuals with FA are uniquely susceptible to oral HPV independent of conventional risk factors.

Funder

National Heart, Lung, and Blood Institute

Center for Clinical and Translational Science, University of Cincinnati

Fanconi Anemia Research Fund

Cincinnati Children’s Hospital-sponsored Translational Research Initiative Grant

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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