HLA-DRB1 and -DQB1 polymorphism in liver recipients: relationship between HLA-DQB1*0302 allele frequency and acute rejection
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Updated: Oct 30, 2026

Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation
Published on: September 6, 2017
M Muro1, M R Alvarez-López, A Torío
1Department of Immunology, University Hospital Virgen de la Arrixaca, Murcia, Spain.
Insights
The HLA-DQB1*0302 allele is linked to acute rejection in liver transplant recipients. This finding suggests HLA-DQB1 genes play a role in graft rejection and tolerance disruption.
Area of Science:
- Immunogenetics
- Transplantation Immunology
Background:
- Human Leukocyte Antigen (HLA) genes are crucial in immune responses and transplantation.
- Understanding HLA polymorphism in liver transplantation is key to managing graft rejection and tolerance.
Purpose of the Study:
- To investigate the association between HLA-DRB1 and HLA-DQB1 polymorphisms and acute rejection in orthotopic liver graft recipients.
- To explore the role of specific HLA alleles in the context of liver transplant rejection episodes.
Main Methods:
- Genotyping of HLA-DRB1 and HLA-DQB1 loci using nonradioactive Southern-blotting hybridization (SSOP) techniques.
- Analysis of DNA from peripheral blood lymphocytes and liver biopsy samples of 53 recipients and 108 healthy controls.
Main Results:
- No significant differences in HLA-DQB1 allele frequencies were found between the overall recipient group and controls.
- A significantly increased frequency of the HLA-DQB1*0302 allele was observed in liver recipients experiencing acute rejection episodes compared to controls or non-rejected patients.
- No significant differences in HLA-DRB1 allele frequencies were detected across study groups.
Conclusions:
- HLA-DQB1 genes, particularly the HLA-DQB1*0302 allele, may be implicated in liver graft rejection.
- These findings contribute to understanding the mechanisms underlying transplant tolerance and its potential disruption in liver recipients.
Abstract:
Polymorphism of HLA-DRB1 and HLA-DQB1 loci was performed in fifty-three orthotopic liver graft recipients as well as in 108 unrelated healthy controls. Nonradioactive SSOPs were used to study PCR-amplified DNA from peripheral blood lymphocytes and biopsied material. The comparison frequency for DQB1 alleles did not reveal any significant differences between the total group of liver recipients and controls. However, when the liver recipients were subgrouped according to their rejection episode manifestations, increased and significant frequencies were observed for HLA-DQB1*0302 allele in patients showing acute rejection episodes compared to healthy controls or patients without acute rejection. This relationship did not appear influenced by the amino acid beta alanine residue in the 57th position. On the other hand, the study of the DRB1 allele frequencies did not show significant differences in any study. These results suggest that HLA-DQB1 genes could be important in the liver graft alloresponses, opening a way to a better understanding of the special tolerance state, normally observed in this type of transplant, leading us to consider the possible HLA-DQB1*0302 allele effect on tolerance rupture.
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