z-logo
Premium
Human papillomavirus load in benign HPV ‐associated oral lesions from HIV / AIDS individuals
Author(s) -
CamachoAguilar S,
RamírezAmador V,
RosendoChalma P,
GuidoJiménez M,
GarcíaCarrancá A,
AnayaSaavedra G
Publication year - 2018
Publication title -
oral diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.953
H-Index - 87
eISSN - 1601-0825
pISSN - 1354-523X
DOI - 10.1111/odi.12732
Subject(s) - human papillomavirus , medicine
Background Although HPV emerged as a crucial carcinogenic and prognostic biomarker in head and neck cancer, and considering the increase in HPV ‐associated oral lesions ( HPV ‐ OL s) in HIV individuals, molecular information about HPV ‐ OL s is scarce; thus, our aim was to determine viral loads in HPV ‐ OL s from HIV / AIDS individuals. Methods HIV / AIDS subjects with HPV ‐ OL were included in this cross‐sectional study. Following informed consent, biopsies were obtained. HPV detection and typing were carried out by PCR and sequencing ( MY 09/11, GP 5+/6+). HPV ‐13 and HPV ‐32 loads were determined by a high‐resolution melting assay. For statistical analysis, X 2 , Fisher's exact, and Mann‐Whitney U tests were applied, using SPSS software (v.23). Results Twenty‐nine HIV subjects (median age 38 years, 93% males) were included. Most were AIDS individuals (72.4%) under HAART (89.7%). Twenty‐two (75.9%) participants had more than one HPV ‐ OL (four with florid presentations), mostly multifocal epithelial hyperplasia (62%), being HPV ‐13 (26%) and HPV ‐32 (31%) the most frequent types. HPV load was higher in individuals with multiple HPV ‐ OL s than in solitary lesions (4.9 vs. 3.2 Log 10 copies/ ml , p  = .090) and in HPV ‐32 + than in HPV ‐13 + (8.3 vs. 6.4 Log 10 copies/ ml , p  = .014). Conclusions Multiple HPV ‐ OL s showed high HPV loads, possibly indicating transcriptional activity of the virus; however, in the HIV setting, the individual and local immunological response could be the key process.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here