# Chronic Hepatitis B Virus Infection and HLA Variations in a Greek Population

**Authors:** Evangelia Myserli, Ioannis Goulis, Asimina Fylaktou, Maria Exindari, Fani Minti, Georgia Chatzika, Eleni Iliopoulou, Polyxeni Agorastou, Ioanna Papagiouvanni, Theodora Oikonomou, Georgia Gioula

PMC · DOI: 10.3390/v17040462 · Viruses · 2025-03-24

## TL;DR

This study explores how specific HLA gene variations are linked to chronic hepatitis B virus infection in a Greek population.

## Contribution

The study identifies HLA alleles associated with susceptibility or protection against chronic HBV in a Greek cohort.

## Key findings

- HLA-C*01 and HLA-DRB1*16 alleles are more frequent in chronic HBV patients than in those with spontaneous clearance.
- HLA-A*01, HLA-B*08, and others show increased frequency in cHBV patients compared to healthy individuals.
- HLA-B*38 allele frequency is significantly lower in chronic HBV patients.

## Abstract

Chronic hepatitis B is linked with considerable liver-related morbidity and mortality globally. Human leukocyte antigen (HLA) polymorphisms affect the susceptibility and outcome of many immune-mediated diseases and infections. Our aim was to study the impact of HLA alleles on HVB-infected individuals in a Greek population. In total, 107 patients with chronic HBV infection (cHBV group) and 101 with spontaneous clearance (SC-group) of hepatitis B surface antigen (HBsAg) were genotyped for HLA-A, HLA-B, HLA-C, HLA-DRB1, and HLA-DQB1 loci by single-specific primer polymerase chain reaction (PCR-SSP). The HLA alleles’ frequencies were compared between the two patient groups and healthy individuals from the North Greece Bone Marrow Donor Registry (14506 samples). We found a significantly increased frequency of HLA-C*01 and HLA-DRB1*16 alleles in the cHBV group versus the SC-group. The frequency of HLA-A*01, HLA-B*08, HLA-C*01, HLA-C*08, HLA-DRB1*03, and HLA-DQB1*05 alleles was significantly higher in cHBV patients versus healthy individuals, while the frequency of the HLA-B*38 allele was significantly lower. Our study showed an association of specific HLA alleles with either susceptibility or protection against chronic HBV infection.

## Linked entities

- **Genes:** HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105], HLA-B (major histocompatibility complex, class I, B) [NCBI Gene 3106], HLA-C (major histocompatibility complex, class I, C) [NCBI Gene 3107], HLA-DRB1 (major histocompatibility complex, class II, DR beta 1) [NCBI Gene 3123], HLA-DQB1 (major histocompatibility complex, class II, DQ beta 1) [NCBI Gene 3119]
- **Diseases:** chronic hepatitis B (MONDO:0005344), hepatitis B virus infection (MONDO:0005344)

## Full-text entities

- **Genes:** HLA-DQB1 (major histocompatibility complex, class II, DQ beta 1) [NCBI Gene 3119] {aka CELIAC1, HLA-DQB, IDDM1}, HLA-B (major histocompatibility complex, class I, B) [NCBI Gene 3106] {aka AS, B-4901, HLAB}, HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}, HLA-DRB1 (major histocompatibility complex, class II, DR beta 1) [NCBI Gene 3123] {aka DRB1, HLA-DR1B, HLA-DRB, SS1}, HLA-C (major histocompatibility complex, class I, C) [NCBI Gene 3107] {aka D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1}
- **Diseases:** HBV infection (MESH:D006509), infected (MESH:D007239), immune-mediated diseases (MESH:C567355), Chronic Hepatitis B Virus Infection (MESH:D019694)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12031174/full.md

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Source: https://tomesphere.com/paper/PMC12031174