Abstract

BackgroundAlthough vaccines for hepatitis B virus (HBV) are highly effective, HBV infections in vaccinees occur. Index samples of breakthrough infections are typically anti-HBc negative but HBV DNA positive with protective anti-HBs levels while HBsAg detection may be delayed or absent. HBsAg mutations have been associated with some vaccine breakthrough cases.MethodsThis research characterizes the serological and molecular profiles of vaccine breakthrough infections in serial samples from two commercially available plasma donor panels. Samples were tested with commercially available assays for HBV antigens and antibodies: HBsAg, HBeAg, anti-HBc, anti-HBc IgM, anti-HBe, and anti-HBs. Different immunoassay approaches for earlier detection of breakthrough infection were explored including hepatitis B core-related antigen (HBcrAg), a research assay for preS2 antigen, and a new prototype ARCHITECT HBsAg assay with improved sensitivity. The prototype HBsAg assay is fully automated and involves no sample pre-treatment. Molecular testing included HBV DNA quantitation and sequencing of preS1, preS2, surface, and basal core promoter/core promoter genes.ResultsAlthough the research preS2 antigen assay allowed earlier detection of the breakthrough infections than current HBsAg assays and HBcrAg, the new prototype ARCHITECT HBsAg assay provided the earliest serologic detection. The ability of the new prototype HBsAg assay to detect HBsAg in the presence of anti-HBs was investigated using known concentrations of native HBsAg mixed with anti-HBs from a vaccinee. The results demonstrated that the prototype ARCHITECT assay is more sensitive in detecting HBsAg in the presence of anti-HBs than current HBsAg assays. Sequencing revealed multiple substitutions in preS1, preS2, and S regions for one panel including a rare D144N substitution associated with vaccine breakthrough that emerged with increasing frequency as the breakthrough infection developed.ConclusionsWhen compared with other immunoassay approaches, the new prototype ARCHITECT HBsAg assay allows earlier detection of vaccine breakthrough infections and more sensitive detection of HBsAg in the presence of anti-HBs. Molecular characterization of longitudinal samples demonstrated the progressive appearance of a rare HBsAg mutation associated with vaccine breakthrough.

Highlights

  • Vaccines for hepatitis B virus (HBV) are highly effective, HBV infections in vaccinees occur

  • Vaccine breakthrough infections differ from typical acute HBV infection where the order of appearance of viral markers in the peripheral blood follows a consistent pattern with hepatitis B viral Hepatitis B viral DNA (DNA) (HBV DNA) followed by hepatitis B surface antigen (HBsAg), hepatitis B e antigen (HBeAg), and antibody to hepatitis B core antigen

  • The presence of anti-HBs early in infection may block the detection of low levels of HBsAg by current assays since HBsAg assays rely on monoclonal antibodies directed at the S protein, the immunodominant ‘a’ determinant, the same protein that is used in recombinant hepatitis B vaccines

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Summary

Introduction

Vaccines for hepatitis B virus (HBV) are highly effective, HBV infections in vaccinees occur. Index samples of breakthrough infections are typically anti-HBc negative but HBV DNA positive with protective antiHBs levels while HBsAg detection may be delayed or absent. Vaccine breakthrough infections differ from typical acute HBV infection where the order of appearance of viral markers in the peripheral blood follows a consistent pattern with hepatitis B viral DNA (HBV DNA) followed by HBsAg, hepatitis B e antigen (HBeAg), and antibody to hepatitis B core antigen (anti-HBc). Resolution of infection in typical acute infection is marked by loss of serum HBsAg and HBV DNA and the appearance of anti-HBs. In contrast, during breakthrough infections, HBV DNA becomes detectable in vaccinated individuals who have protective levels of anti-HBs. HBsAg detection may be delayed, transient, or absent

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