Abstract

BackgroundInfection with the hepatitis B virus (HBV) is an independent risk factor for liver cirrhosis and hepatocellular carcinoma, polymorphisms in HLA-DQB1 play an important role in HBV infections.MethodsThis study examined the relationships between HLA-DQB1 alleles and HBV infection susceptibility among 256 HBV carriers and 433 healthy controls. Venous blood samples were subjected to DQB1 high-resolution typing and testing for interferon-gamma, interleukin-4 (IL-4), interleukin-10, and DQB1 mRNA expression. A meta-analysis was also performed using relevant case–control studies that evaluated the associations of HLA-DQB1 alleles with HBV infection and clearance.ResultsWe found that HLA-DQB1*06:03 protected against HBV infection. Levels of IFN-γ and IL-4 were significantly elevated in HBV cases with HLA-DQB1*06:05 (vs. HLA-DQB1*05:03), and the HBV group had higher DQB1 mRNA expression than the healthy control group with HLA-DQB1*05:03 and HLA-DQB1*06:02. The meta-analysis revealed that HLA-DQB1*04:01, HLA-DQB1*05:02, HLA-DQB1*05:03, and HLA-DQB1*06:01 were risk factors for HBV infection susceptibility, while HLA-DQB1*05:01, HLA-DQB1*06:03, and HLA-DQB1*06:04 protected against HBV infection. Spontaneous HBV clearance was associated withHLA-DQB1*06:04, while chronic HBV infection was associated with HLA-DQB1*02:01 and HLA-DQB1*05:02.ConclusionDBQ1 typing can be used to identify patients who have elevated risks of HBV infection (i.e., patients with HLA-DQB1*04:01, HLA-DQB1*05:02, HLA-DQB1*05:03, and HLA-DQB1*06:01) or elevated risks of chronic HBV infection (i.e., patients with HLA-DQB1*02:01 and HLA-DQB1*05:02).

Highlights

  • Infection with the hepatitis B virus (HBV) is an independent risk factor for liver cirrhosis and hepatocellular carcinoma, polymorphisms in human leukocyte antigens (HLA)-DQB1 play an important role in HBV infections

  • The results indicated that carriage of HLA-DQB1*06:03 protected against chronic HBV infection (Table 1)

  • In the HBV group, significantly higher levels of IFN-γ and IL-4 were associated with HLA-DQB1*05:01 and *06:05, compared to HLA-DQB1*05:03 (Figs. 1, 2)

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Summary

Introduction

Infection with the hepatitis B virus (HBV) is an independent risk factor for liver cirrhosis and hepatocellular carcinoma, polymorphisms in HLA-DQB1 play an important role in HBV infections. The HBV vaccine became widespread in China during 1992, and the seroprevalence of hepatitis B surface antigen (HBsAg) has decreased to approximately 5.49% in 2015 [3]. Multiple factors influence the risk of chronic HBV infection or spontaneous HBV clearance, such as age, location, sex, body mass index, ethnicity, viral mutation, HBV virus genotype, host genetic variations, and host immune responses. In this context, human leukocyte antigens (HLA) play key roles in mediating the immune response.

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