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Updated: May 16, 2026

Real-Time Polymerase Chain Reaction-Based Detection and Quantification of Hepatitis B Virus DNA
Published on: December 15, 2023
Association analysis between SNPs in IL-28B gene and the progress of hepatitis B infection in Han Chinese
1Department of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, PR China.
Insights
The IL-28B rs12979860 C/T polymorphism T allele is more common in hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC) patients than in liver cirrhosis (LC) patients. This allele may increase HCC development risk.
Area of Science:
- Genetics
- Hepatology
- Virology
Background:
- Hepatitis B virus (HBV) infection can lead to liver cirrhosis (LC) and hepatocellular carcinoma (HCC).
- Interleukin-28B (IL-28B) gene polymorphisms have been associated with HBV infection outcomes.
- Single nucleotide polymorphisms (SNPs) in IL-28B may influence disease progression.
Purpose of the Study:
- To investigate the association between IL-28B gene SNPs and the occurrence of LC and HCC in HBV-infected individuals.
- To determine if specific IL-28B polymorphisms are risk factors for developing advanced liver disease.
Main Methods:
- A candidate gene association study was conducted on Chinese Han subjects.
- Genomic DNA was analyzed from 406 LC and 406 HCC patients caused by chronic hepatitis B (CHB).
- SNP rs12979860 in IL-28B was detected using high-resolution melting curve analysis, with verification in independent cohorts.
Main Results:
- A significant difference in the frequency of rs12979860 was observed between CHB patients who progressed to LC or HCC (p = 0.046).
- Patients with HCC more frequently carried the T allele at rs12979860 compared to LC patients.
- These findings were consistent in an independent sample verification.
Conclusions:
- The T allele of the IL-28B rs12979860 C/T polymorphism is more prevalent in HCC patients than in LC patients.
- Carriage of the IL-28B rs12979860 T allele may increase the risk of developing HCC.
- IL-28B gene polymorphism might influence the symptomatic specificity and progression of hepatitis B infection.
Objective:
As a candidate gene association study, we investigated the genetic association of SNPs in IL-28B genes with different outcomes of HBV infection, including LC and HCC occurrence.
Methods:
Chinese Han subjects were categorized into two groups: 406 LC caused by CHB and 406 HCC caused by CHB. Genomic DNA was isolated from whole blood samples, SNPs were detected using high resolution melting curve (HRM) method. PCR amplification was carried out under the same conditions in a 96-well plate in Real-Time PCR System. Then 341 LC and 356 HCC patients caused by HBV infection were analyzed as a verification by independent sample. 393 CHB patients and 244 health subjects were included as control.
Results:
CHB patients who progress to LC or HCC showed a significant different frequency in rs12979860 (p = 0.046). Patients with HCC carried more frequently the T alleles in rs12979860 comparison to LC. Same results were found in the independent sample.
Conclusion:
IL-28B rs12979860 C/T polymorphism T allele appears to be more prevalent in patients with HCC than in LC. Carriage of this allele seems to enhance the risk for developing HCC. Gene polymorphism of IL-28B may confer symptomatic specificity in progress and extent of hepatitis B infection.
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