乙型肝炎表面抗原
HBeAg
人类白细胞抗原
抗原
抗体
免疫学
病毒学
乙型肝炎病毒
等位基因
乙型肝炎
生物
医学
基因
病毒
遗传学
作者
Xinze Li,Qiaomiao Zhou,Zhe Lü,Renliang Huang,Dan Lin,Jing Xu,Xinhua Yu,Xuexia Li
摘要
Abstract Antigen presentation by HLA class II molecules to CD4 + T cells is an essential step for generating antibodies to hepatitis B antigens. In this study, we investigated the association between the HLA‐DRB1 gene and the status of antibodies to hepatitis B surface and e antigens. Our results revealed a significant association between the status of anti‐HBsAg and HLA‐DRB1*04:03 (OR = 4.11, 95% CI = 1.50–10.84, p = 0.005, P adj. = 0.05) as well as HLA‐DRB1*15:01 (OR = 1.74, 95% CI = 1.20–2.50, p = 0.002, P adj. = 0.045). MHC II binding predictions and in silico docking demonstrated strong binding affinity of HBsAg peptides to these two HLA‐DRB1 molecules. Conversely, the status of anti‐HBeAg was inversely associated with HLA‐DRB1*14:54 (OR = 0.34, 95% CI = 0.18–0.64, p = 0.001, P adj. = 0.011), and in silico analysis revealed weak binding affinity of HBeAg peptides to HLA‐DRB1*14:54. In conclusion, these findings support the involvement of HLA‐DRB1 in humoral immunity against HBV infection.
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