Evaluation of a personalized, dose-sparing revaccination strategy in hepatitis B vaccine non-responders

•The baseline anti-HBs titre in non-responders affects the seroconversion rate after revaccination.•Agreement of assays to differentiate between presence or absence of anti-HBs below the titre of 10 IU/L was substantial, except for ADVIA.•The limit of detection is a reliable cutoff to differentiate...

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Veröffentlicht in:Vaccine 2022-05, Vol.40 (23), p.3210-3215
Hauptverfasser: Beulens, Christian, Raven, Stijn F.H., van Jaarsveld, Cornelia H.M., van Loo, Inge, Boland, Greet, Visser, Leo G., Hoebe, Christian J.P.A., Vossen, Ann C.T.M.
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Sprache:eng
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Zusammenfassung:•The baseline anti-HBs titre in non-responders affects the seroconversion rate after revaccination.•Agreement of assays to differentiate between presence or absence of anti-HBs below the titre of 10 IU/L was substantial, except for ADVIA.•The limit of detection is a reliable cutoff to differentiate between a zero- and poor- responder.•The titre-based strategy results in a reduction of revaccinations needed compared to the standard series. The detection of low levels of antibodies against HBsAg (anti-HBs) below 10 IU/L in non-responders after a primary hepatitis B vaccination, is associated with seroconversion after revaccination. We compared the diagnostic performance of four anti-HBs assays in non-responders in their ability to differentiate between absence or presence of low levels of anti-HBs and propose a revaccination strategy guided by anti-HBs titres. Non-responders were revaccinated with Fendrix 20 μg at 0, 1 and 2 months. Anti-HBs titres were determined by Abbott Architect, Diasorin Liaison, Roche Cobas and Siemens ADVIA Centaur. Inter-assay agreement was evaluated with Cohen’s Kappa (k) in baseline samples between zero-responders without detectable antibodies and poor-responders with detectable antibodies 
ISSN:0264-410X
1873-2518
DOI:10.1016/j.vaccine.2022.04.042