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Published on: July 9, 2014
GB virus C (GBV-C/HGV) and E2 antibodies in children preliver and postliver transplant
O Elkayam1, H M Hassoba, L D Ferrell
1Department of Pediatrics, University of California, San Francisco, 94143, USA.
Insights
GB virus type C (GBV-C) infection is common in children after liver transplants, often acquired through blood transfusions. However, GBV-C RNA did not correlate with post-transplant hepatitis incidence or severity.
Area of Science:
- Hepatology
- Virology
- Transplant Immunology
Background:
- The clinical significance of GB virus type C (GBV-C) remains uncertain.
- The role of GBV-C and its E2 antibody in pediatric liver transplant recipients is undetermined.
Purpose of the Study:
- To determine the prevalence of GBV-C in children undergoing liver transplantation.
- To assess the association between GBV-C infection and post-transplant hepatitis.
- To evaluate the protective role of GBV-C E2 antibodies.
Main Methods:
- Sera from 34 pediatric liver transplant patients (pre- and post-transplant) were tested for GBV-C RNA using PCR.
- Anti-E2 antibodies were detected via immunoassay.
- Post-transplant liver biopsies were analyzed for hepatitis.
Main Results:
- GBV-C RNA prevalence increased from 12% pre-transplant to 42% post-transplant, with a 33% conversion rate.
- GBV-C acquisition correlated with the number of blood product units received.
- No significant difference in hepatitis incidence or severity was observed between GBV-C RNA positive and negative children.
- Pre-existing anti-E2 antibodies did not prevent GBV-C acquisition post-transplant.
Conclusions:
- GBV-C infection is highly prevalent in pediatric liver transplant recipients, with blood transfusions being a likely source of acquisition.
- GBV-C infection is not associated with the development or severity of post-transplant hepatitis in this cohort.
- Pre-transplant E2 antibody presence offers incomplete protection against GBV-C infection.
Abstract:
The association of GB virus type C (GBV-C) virus and clinical disease is uncertain. The role of GBV-C and (Envelope) E2 antibody in children with liver transplants has not been determined. This study's aim is to examine the prevalence of GBV-C in children with liver transplants, to assess the relationship of GBV-C to posttransplant hepatitis, and to determine the role of E2 antibodies. Sera from 34 children, preliver and postliver transplant, between 1989-1996 were tested for GBV-C (Ribonucleic acid) RNA by the automated Abbott LCx PCR assay. Anti-E2 antibodies were detected by an Abbott immunoassay. Recent posttransplant liver biopsies were examined for hepatitis. The results of the study determined that pretransplant, four children (12%) were GBV-C RNA positive. Posttransplant, 14 (42%) children were GBV-C RNA positive. The GBV-C RNA positive conversion rate was 33% (CI 17.2-55.7%). Patients received blood products from a mean of 68 +/- 34 donors, which correlated with GBV-C acquisition. There was no difference in the incidence (32%versus 36%; p = 0.726) or severity (grade 2.00 versus 0.68; p = 0.126) of posttransplant hepatitis in the liver biopsies of GBV-C RNA negative and/or positive children, respectively. Pretransplant, nine of 32 children were anti-E2 positive. Posttransplant, eight of 32 children were anti-E2 positive, including five children who were anti-E2 positive pretransplant. Of nine children who were anti-E2 positive and GBV-C RNA negative pretransplant, three became GBV-C RNA positive posttransplant. The results of this study conclude that the prevalence of GBV-C infection in children postliver transplantation is high and that blood product transfusions correlate with GBV-C acquisition. Also, no correlation was found between GBV-C RNA and the incidence or severity of posttransplant hepatitis. Finally, E2 antibody presence before transplantation failed to provide complete protection from GBV-C acquisition.
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