Key result
IL28B rs8099917 polymorphisms in the recipient or donor were not independent predictors of sustained virologic response in HCV patients after living donor liver transplantation.
Why the study?
Do donor and recipient single nucleotide polymorphisms of IL28B rs8099917 affect virologic response to preemptive interferon and ribavirin treatment in living donor liver transplantation for Hepatitis C?
Cohort (n=96)
Do donor and recipient single nucleotide polymorphisms of IL28B rs8099917 affect virologic response to preemptive interferon and ribavirin treatment in living donor liver transplantation for Hepatitis C?
IL28B polymorphisms in either the recipient or donor are not independent factors for achieving sustained virologic response to preemptive interferon and ribavirin after living donor liver transplantation for HCV.
IL28B rs8099917 testing should not guide donor selection or preemptive therapy post-transplant; leaves open whether other factors predict sustained virologic response.
Single nucleotide polymorphisms of interleukin-28B (IL28B) rs8099917 are reported to be associated with virologic clearance in interferon-and ribavirin -based treatment for hepatitis C virus (HCV)-infected patients. We examined virologic response in accordance with IL28B polymorphisms in our living donor liver transplantation series under a preemptive interferon and RBV treatment approach. Adequate DNA samples from both the recipient and donor for the study of single nucleotide polymorphisms of IL28B were available from 96 cases and were the subjects of the present study. Various clinical factors related with virologic response including early virologic response (EVR) and sustained virologic response (SVR) were examined. Totally 51% presented with EVR and 44% achieved SVR. Presence of the major allele (TT) in either the recipient or the donor corresponded to SVR of 53% and 48%. Presence of the minor allele (TG or GG) corresponded to SVR of 26% and 32%. Multivariate analysis revealed that genotype of HCV or EVR, but not IL28B polymorphisms in either the recipient or donor, was an independent factor for achieving SVR. When virologic response to treatment was incorporated into analysis, the impact of IL28B polymorphism on virological clearance remained relative to other factors and was not significantly independent.
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Harada et al. (2014) conducted a cohort in Hepatitis C (n=96). IL28B rs8099917 major allele (TT) vs. IL28B rs8099917 minor allele (TG or GG) was evaluated on Sustained virologic response (SVR). IL28B rs8099917 polymorphisms in the recipient or donor were not independent predictors of sustained virologic response in HCV patients after living donor liver transplantation.
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