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HLA-DRB1 Class II antigen level alleles are associated with persistent HPV infection in Mexican women; a pilot study

Authors :
Ricardo M. Cerda-Flores
Hilario Flores-Aguilar
José Morales-Casas
Hugo A. Barrera-Saldaña
Lezmes D. Valdez-Chapa
Carmen Alaez
Sofía Bernal-Silva
Juan Francisco González-Guerrero
Clara Gorodezky
Geraldina Guerrero-González
Julio Granados
Source :
Infectious Agents and Cancer
Publisher :
Springer Nature

Abstract

Background Persistent infection with high-risk human papillomavirus (HPV) is a major risk factor for malignant lesions and cervical cancer. A widely studied element in the search for genetic factors influencing risk HPV infection diseases is allelic variation of the human leukocyte antigen (HLA) locus. The study was designed to search for HLA susceptibility alleles contributing to the persistence of HPV infection in Mexican women. Methods A total of 172 subjects were divided into three groups: 1) HPV–persistent patients; 2) HPV–cleared; and 3) HPV–reinfected patients. They were screened for HPV types using a polymerase chain reaction (PCR). PCR-sequence specific oligonucleotide probes (PCR-SSOP) was used for HLA DRB1 and DQB 1 typing. Results We observed that HLA-DQB1*0501 allele might be associated with susceptibility of reinfection with HPV (p = 0.01, OR = 4.9, CI 95% = 1.3 -18.7). Allele frequency of HLA-DRB1*14 was particularly reduced in patients with cancer when compared with the HPV–persistent group (p = 0.04), suggesting that this allele is a possible protective factor for the development of cervical cancer (OR = 2.98). HLA-DRB1*07 might be associated with viral clearance (p = 0.04). Conclusions Genetic markers for HPV infection susceptibility are different in each population, in Mexicans several HLA-DQB1 alleles might be associated with an enhanced risk for viral persistence. In contrast, DRB1*14, seems to confer protection against cervical cancer.

Details

Language :
English
ISSN :
17509378
Volume :
8
Issue :
1
Database :
OpenAIRE
Journal :
Infectious Agents and Cancer
Accession number :
edsair.doi.dedup.....ba7fb6ee5c8201ea15aaac7deca4eae7
Full Text :
https://doi.org/10.1186/1750-9378-8-31