Carcinoma, Hepatocellular, End Stage Liver Disease, Hepatitis B, Hepatitis B, Chronic
Conditions
Brief summary
In this project proposal, the investigators will investigate the genetic alterations of Hepatitis B Virus (HBV) strains circulating in Belgian patients who developed end stage liver disease. Additionally, the investigators will compare and link these data sets with three genetic factors involved in immune system response.
Detailed description
This project proposes to identify and characterize the genetic alterations associated with intra-host evolution of HBV from a chronically infection status to an end-stage liver disease status.
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
Study group: * Clinical diagnosis of advanced liver disease related to chronic Hepatitis B infection (cirrhosis, hepatocellular carcinoma,..) * Availability of serum samples Control group: * Clinical diagnosis of liver disease related to chronic Hepatitis B infection in a pre-advanced stage * Matched demographic and geographic characteristics to study group * Availability of serum samples
Exclusion criteria
* Liver disease caused by other hepato-tropic viruses * Patients with auto-immune diseases
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| genetic variants of Hepatitis B | 6 months | Virus variants will be identified by amino acid or nucleotide variations (insertions or deletions) in different Open Readind Frames (ORFs) of the HBV genome by using next-generation sequencing. Comparison of virus variants within one patient Comparison of virus variants between patients with end stage liver disease and patients with a chronic Hepatitis B infection. Determination of the viral load by quantitative Polymerase Chain Reaction (PCR). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| genetic variation in host-specific immune markers | at day of enrollment | Amplification of HLA-A, HLA-B, HLA-C class I and HLA class II using PCR methods and next-generation sequencing Amplification of KIR genes: 2DS1, 2DS2, 2DS3, 2DS4, 2DS5, 3DS1 and 1D, 2DL1 2DL2, 2DL3, 2DL5 and 3DL1 using PCR methods and next-generation sequencing Amplification of SNPs in TNF alfa, TGF beta1 and IFN-R using PCR methods and next-generation sequencing |
Countries
Belgium