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Published on: July 16, 2012
Hepatitis C virus compartmentalization and infection recurrence after liver transplantation
S Ramirez1, S Perez-Del-Pulgar, J A Carrion
1Liver Unit. Institut de Malalties Digestives, CIBERehd, IDIBAPS and University of Barcelona, Barcelona, Spain .
Insights
Hepatitis C virus (HCV) compartmentalization is significant in liver transplant patients. Viral variants from the liver drive HCV recurrence post-transplant, impacting pathogenesis.
Area of Science:
- Virology
- Immunology
- Hepatology
Background:
- Hepatitis C virus (HCV) compartmentalization influences infection pathogenesis.
- Understanding HCV compartmentalization is crucial in liver transplantation (LT).
Purpose of the Study:
- To investigate the presence and relevance of HCV compartmentalization in patients undergoing liver transplantation.
- To identify the source of viral variants causing HCV recurrence after LT.
Main Methods:
- Collected serum, PBMC, PLN, and liver explant samples from 57 HCV-cirrhotic patients undergoing LT.
- Quantified HCV-RNA levels using real-time PCR and sequenced the hypervariable region 1 (HVR-1).
- Analyzed viral sequences from distinct body compartments.
Main Results:
- HCV-RNA detected in all samples from untreated control patients.
- Recurrence post-LT in responders linked to residual HCV-RNA in liver explants.
- 47% of patients showed sequence differences across compartments; recurrence sequences matched liver/serum isolates from LT time.
Conclusions:
- A significant proportion of HCV-infected patients exhibit viral compartmentalization.
- Liver-derived viral variants are the primary cause of HCV recurrence following liver transplantation.
Abstract:
Hepatitis C virus (HCV) compartmentalization may have important implications in the pathogenesis of HCV infection. The aim of this study was to investigate the presence and relevance of HCV compartmentalization in the setting of liver transplantation (LT). We collected samples of serum, peripheral blood mononuclear cells (PBMC), perihepatic lymph nodes (PLN) and liver explant at the time of LT, and serum and PBMC after transplantation from 57 HCV-infected cirrhotic patients undergoing LT: 38 individuals received antiviral treatment before LT and 19 were untreated controls. HCV-RNA levels were determined by real-time PCR and the hypervariable region 1 (HVR-1) was sequenced. HCV-RNA was detected in all samples from control patients. In virological responders, recurrence after LT was associated with residual HCV-RNA in the liver explant. Within the entire cohort, 47% of patients harbored differences in direct sequences from distinct compartments. Quasispecies analysis revealed that in most cases, HVR-1 sequences recovered after infection recurrence were identical or closely related to those isolated from the liver explant and serum at the time of LT. Our study shows that a significant proportion of HCV-infected cirrhotic patients exhibit compartmentalization. Viral variants originating within the liver appear to be the main cause of HCV recurrence after LT.
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