Gokhale Priyanka, Kerkar Shilpa, Tongaonkar Hemant, Chaudhari Hemangi, Warke Himangi, Salvi Vinita, Mania-Pramanik Jayanti
National Institute for Research in Reproductive Health (ICMR), Mumbai, India.
Indian J Med Res. 2014 Nov;140 Suppl(Suppl 1):S36-43.
BACKGROUND & OBJECTIVES: Human papillomavirus (HPV) is the main causative agent for cervical cancer. Variability in host immunogenetic factors is important in determining the overall cellular immune response to the HPV infection. This study was carried out to confirm the association between human leukocyte antigen (HLA) class II alleles and cervical cancer in HPV infected women.
Both low and high resolution methods were used to genotype HLA class II (DRB1 and DQB1) alleles in 75 women with cervical cancer (cases) and 75 HPV positive women and 100 HPV negative women with healthy cervix (controls). odds ratio and 95% confidence interval were calculated. Co-occurring HLA alleles (haplotype) across cases and controls were also studied.
Significant association was found for HLA-DRB103(13:01) and - DQB102(02:01) with increased risk for cervical cancer. Also, HLA-DRB113(13:01); -DQB106 and -DQB103:02 were significantly associated with decreased risk for cervical cancer. Haplotype analysis highlighted the significant association of HLA- DRB107:01-DQB102:02 and HLA DRB110:01-DQB105:01 with cervical cancer, while HLA-DRB114:04-DQB105:03 and DRB115:01-DQB106:01 conferred decreased risk for cervical cancer. Multivariate analysis highlighted the association of specific alleles with cervical cancer after adjusting for confounding factor age.
INTERPRETATION & CONCLUSIONS: There were possible associations of specific HLA class II alleles either with risk of developing cervical cancer, or with its protection. Our results confirmed the assessment of DRB113 as a protective marker in HPV infection outcome. our study also revealed protective association of homozygous haplotype DRB115- DQB1*06 with cervical cancer.
人乳头瘤病毒(HPV)是宫颈癌的主要致病因子。宿主免疫遗传因素的变异性对于确定整体细胞对HPV感染的免疫反应很重要。本研究旨在证实人白细胞抗原(HLA)II类等位基因与HPV感染女性宫颈癌之间的关联。
采用低分辨率和高分辨率方法对75例宫颈癌女性(病例组)、75例HPV阳性女性以及100例宫颈健康的HPV阴性女性(对照组)的HLA II类(DRB1和DQB1)等位基因进行基因分型。计算比值比和95%置信区间。还研究了病例组和对照组中同时出现的HLA等位基因(单倍型)。
发现HLA-DRB103(13:01)和-DQB102(02:01)与宫颈癌风险增加显著相关。此外,HLA-DRB113(13:01)、-DQB106和-DQB103:02与宫颈癌风险降低显著相关。单倍型分析突出了HLA-DRB107:01-DQB102:02和HLA DRB110:01-DQB105:01与宫颈癌的显著关联,而HLA-DRB114:04-DQB105:03和DRB115:01-DQB106:01则使宫颈癌风险降低。多变量分析突出了在调整混杂因素年龄后特定等位基因与宫颈癌的关联。
特定的HLA II类等位基因可能与患宫颈癌的风险或其保护作用存在关联。我们的结果证实了将DRB113评估为HPV感染结果中的一个保护标志物。我们的研究还揭示了纯合单倍型DRB115-DQB1*06与宫颈癌的保护关联。