Apolipoprotein H expression is associated with IL28B genotype and viral clearance in hepatitis C virus infection

10Citations
Citations of this article
39Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Background & Aims: HCV requires host lipid metabolism for replication, and apolipoproteins have been implicated in the response to treatment. Methods: We examined plasma apolipoprotein concentrations in three cohorts of patients: mono-infected patients with symptomatic acute hepatitis C (aHCV); those undergoing treatment for chronic hepatitis C (cHCV); and HIV/HCV co-infected patients being treated for their chronic hepatitis C. We also evaluated associations between apolipoproteins and IL28B polymorphisms, a defined genetic determinant of viral clearance. Results: Plasma apolipoprotein H (ApoH) levels were significantly higher in patients who achieved spontaneous clearance or responded to pegylated-interferon/ribavirin therapy. Strikingly, patients carrying the IL28B rs12979860 CC SNP correlated with the plasma concentration of ApoH in all three cohorts. Both ApoH and IL28B CC SNP were associated with HCV clearance in univariate analysis. Additional multivariate analysis revealed that the association between IL28B and HCV clearance was closely linked to that of Apo H and HCV clearance, suggesting that both belong to the same biological pathway to clearance. The association between IL28B CC SNP and ApoH was not observed in healthy individuals, suggesting that early post-infection events trigger differential ApoH expression in an IL28B allele dependent manner. Conclusions: This relationship identifies ApoH as the first induced protein quantitative trait associated with IL28B, and characterises a novel host factor implicated in HCV clearance.

Cite

CITATION STYLE

APA

Laird, M. E., Mohsen, A., Duffy, D., Mamdouh, R., LeFouler, L., Casrouge, A., … Fontanet, A. (2014). Apolipoprotein H expression is associated with IL28B genotype and viral clearance in hepatitis C virus infection. Journal of Hepatology, 61(4), 770–776. https://doi.org/10.1016/j.jhep.2014.05.040

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free