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DRB1 alleles in relation to severity of liver disease in patients with chronic hepatitis C
W Kryczka1, E Brojer, A Kalińska
1Probationary Infectious Diseases Department, Voivod Hospital, ul. Radiowa 7, 25-317 Kielce, Poland.
Insights
Specific human leukocyte antigen (HLA) class II alleles are linked to chronic hepatitis C (CHC) liver disease severity. DRB1*13 and DRB1*07 correlate with increased inflammation, while DRB1*11 is associated with milder liver damage.
Area of Science:
- Immunogenetics
- Hepatology
- Virology
Background:
- Chronic hepatitis C (CHC) poses a significant global health challenge.
- Understanding host genetic factors, like human leukocyte antigen (HLA) class II alleles, is crucial for predicting disease progression.
- The relationship between specific HLA class II antigens and liver disease severity in CHC patients requires further elucidation.
Purpose of the Study:
- To analyze the association between HLA class II antigens and the severity of liver disease in patients with chronic hepatitis C.
- To investigate the correlation of specific HLA DRB1 alleles with necroinflammatory activity and liver fibrosis progression in CHC.
Main Methods:
- Analysis of data from 134 histopathologically confirmed CHC patients (HCV RNA-positive, HBsAg-negative, HIV-negative).
- Liver biopsy assessment using Ishak's criteria for grading (necroinflammation) and staging (fibrosis).
- Determination of HLA DRB1 alleles using the INNOLiPA DRB method; statistical analysis of alleles with >10% frequency.
Main Results:
- A statistically significant correlation was observed between DRB1*13 and DRB1*07 alleles and increased necroinflammatory activity.
- The DRB1*13 allele was also significantly associated with the progression of liver disease.
- Conversely, the DRB1*11 allele showed a statistically significant relationship with milder liver damage.
Conclusions:
- Specific HLA class II alleles, particularly DRB1*13, DRB1*07, and DRB1*11, play a role in modulating the immune response and influencing the severity and progression of liver disease in chronic hepatitis C.
- These findings highlight the potential of HLA genotyping for predicting disease outcomes in CHC patients.
- Further research may explore therapeutic strategies targeting HLA-mediated immune responses in CHC.
Abstract:
The aim of our study was analysis of relation between HLA class II antigens and the liver disease severity in chronic hepatitis C (CHC) patients. The subject of analysis was data obtained from 134 CHC patients with disease confirmed by histopathologic test (F/M: 62/72; age 16-74; average age 41.4 +/- 12.7 yrs), HCV RNA-positive, HbsAg- and HIV-negative with no coexistence of any other liver diseases. Liver biopsy specimens were estimated according to Ishak's criterions (grading 0-18; staging 0-6). HLA DRB1 alleles were determined by a commercial method INNOLiPA DRB (Innogenetics, Belgium). Statistical analysis considered alleles occurring with frequency higher than 10%. The necroinflammatory activity (average grading score) was compared in groups of patients with- and without particular allele. The frequency of each allele's occurrence was analyzed according to patients sex, age and staging score of liver fibrosis. In statistical analysis t-Student test and chi-squared test with or without Yates' correction were applied. Statistically significant correlation was found between occurrence of DRB1*13 and DRB1*07 alleles and necroinflammatory activity intensification, and between occurrence of DRB1*13 allele and progression of liver disease. Mild liver damage, instead, expresses statistically significant relation with DRB1*11 allele.
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