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Assessment of Hepatitis B Virus Intra-host Population and Host-specific Immune Marker Diversity

Assessment of Hepatitis B Virus Intra-host Population and Host-specific Immune Marker Diversity With Next-generation Sequencing: From Chronic Infection to End-stage Liver Disease and Liver Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02148562
Enrollment
274
Registered
2014-05-28
Start date
2014-04-30
Completion date
2017-12-31
Last updated
2014-05-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carcinoma, Hepatocellular, End Stage Liver Disease, Hepatitis B, Hepatitis B, Chronic

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

Fund for Scientific Research, Flanders, Belgium
CollaboratorOTHER
Universitaire Ziekenhuizen KU Leuven
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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

MeasureTime frameDescription
genetic variants of Hepatitis B6 monthsVirus 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

MeasureTime frameDescription
genetic variation in host-specific immune markersat day of enrollmentAmplification 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

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026