Effect of HLA-DPA1 alleles on chronic hepatitis B prognosis and treatment response

Seyma Katrinli1, Feruze Yilmaz Enc2, Kamil Ozdil3

  • 1Department of Molecular Biology and Genetics, Istanbul Technical University, Istanbul, Turkey.

Insights

The HLA-DPA1*04:01 allele may increase the risk of chronic hepatitis B (CHB) recurrence after hepatitis B e antigen (HBeAg) seroconversion. This specific allele was more common in patients who experienced disease reoccurrence.

Area of Science:

  • Immunogenetics
  • Hepatology
  • Virology

Background:

  • Chronic hepatitis B (CHB) poses a significant global health challenge.
  • Hepatitis B virus (HBV) infection outcomes are influenced by human leukocyte antigen (HLA) variations.
  • HLA-DPA1 alleles are implicated in the course of HBV infection.

Purpose of the Study:

  • To examine the association between HLA-DPA1 alleles and treatment response in CHB patients.
  • To investigate the link between HLA-DPA1 alleles and hepatitis B e antigen (HBeAg) seroconversion.
  • To determine if HLA-DPA1 alleles correlate with disease recurrence post-HBeAg loss.

Main Methods:

  • Genotyping of eight HLA-DPA1 alleles in 246 CHB patients using high-resolution polymerase chain reaction with sequence-specific primers.
  • Analysis of associations with treatment response, cirrhosis development, HBeAg seroconversion, and disease recurrence.
  • Statistical analysis including Fisher's exact test for significance.

Main Results:

  • No significant association was found between HLA-DPA1 alleles and treatment response, cirrhosis development, or HBeAg seroconversion.
  • The HLA-DPA1*04:01 allele was significantly more prevalent in patients who experienced disease reoccurrence after HBeAg seroconversion (100% vs. 36.8%, p=0.037).

Conclusions:

  • The HLA-DPA1*04:01 allele may serve as a predictive marker for CHB reoccurrence.
  • Further research is warranted to elucidate the mechanisms underlying this association.
  • Understanding HLA-DPA1 associations can inform personalized management strategies for CHB.
Abstract

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