华西虚拟期刊

华西虚拟期刊

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Although the SLE risk gene loci of HLA-DR and HLA-DQ within the major histocompatibility complex (MHC) region has been gradually revealed by recent Genome-Wide Association studies (GWAS), the association of HLA-DP polymorphisms with SLE was minimally reported. Considering that the variants in rs3077 and rs9277535 in the HLA-DP region could influence the immune response by affecting antigen presentation of HLA class II molecules to CD4(+) T cells, the present study aimed to explore the role of HLA-DP polymorphisms in SLE. In total, samples from 335 SLE patients and 635 healthy controls were collected and genotyped by a polymerase chain reaction-high resolution melting (PCR-HRM) assay. A significant positive correlation was observed between the SNP rs3077, rs9277535 of HLA-DP and SLE susceptibility (rs3077, OR = 0.74, 95% CI = 0.60-0.91, P = 0.004; rs9277535, OR = 0.72, 95% CI = 0.59-0.88, P = 0.001). Rs3077 polymorphism was corelated to IL-17, INF-gamma and cutaneous vasculitis (P = 0.037, P = 0.020 and P = 0.006, respectively). Additionally, rs3077 AA genotype carriers showed lower concentration of inflammatory cytokines and lower cutaneous vasculitis incidence than did the other two genotype. No significant association was observed between rs9277535 and cytokines or any clinical features. In conclusion, HLA-DP polymorphisms (rs3077 and rs9277535) were associated with SLE susceptibility and the levels of some inflammatory cytokines in SLE patients.

Key words: GENOME-WIDE ASSOCIATION; CHRONIC HEPATITIS-B; HEPATOCELLULAR-CARCINOMA DEVELOPMENT; VIRUS INFECTION; IFN-ALPHA; SUSCEPTIBILITY; VARIANTS; LOCI; ALLORECOGNITION; CLEARANCE

引用本文: . . 华西虚拟期刊, 2000, 1(1): -. doi: 10.1038/srep39757 复制

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