Association of HLA-DRB1 alleles with status of antibodies to hepatitis B surface and e antigen

被引:1
|
作者
Li, Xinze [1 ,2 ]
Zhou, Qiaomiao [1 ]
Lu, Zhe [1 ]
Huang, Renliang [1 ]
Lin, Dan [1 ]
Xu, Jing [1 ]
Yu, Xinhua [1 ,3 ]
Li, Xuexia [2 ]
机构
[1] Hainan Women & Childrens Med Ctr, Haikou 571199, Hainan, Peoples R China
[2] Hainan Med Univ, Sch Trop Med, NHC Key Lab Trop Dis Control, Haikou 571199, Hainan, Peoples R China
[3] Res Ctr Borstel, Prior Area Chron Lung Dis, D-23845 Borstel, Germany
基金
中国国家自然科学基金;
关键词
antigen presentation: immune responses; anti-hepatitis B virus antivirals: antiviral agents; genetics; HLA; SEROCONVERSION; CHILDREN; VIRUS;
D O I
10.1002/jmv.29867
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
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页数:7
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