Analytical performance evaluation of MAGLUMI HBeAg and anti-HBe chemiluminescence immunoassays and comparison with the Abbott assays
Rattachement africain : cn, jp. Niveau de preuve : code pays fourni par la source.
Le résumé fourni par la source
Background: Hepatitis B e antigen (HBeAg) and its corresponding antibody (anti-HBe) serve as critical serological markers in the evaluation and therapeutic management of Hepatitis B virus (HBV) infection. Study design: This retrospective study was designed to evaluate the performance of the newly CE-marked MAGLUMI HBeAg (CLIA) and MAGLUMI Anti-HBe (CLIA) assays by comparing with Abbott Architect HBeAg and Abbott Architect Anti-HBe assays, respectively. Analytical performance was verified in compliance with the guidelines issued by the Clinical and Laboratory Standards Institute (CLSI). Negative and positive specimens were collected to determine negative percent agreement (NPA) and positive percent agreement (PPA) respectively. Analytical specificity was assessed using negative samples containing potentially cross-reacting substances. Additionally, analytical sensitivity was evaluated using 1st WHO International Standard. Results: The claimed performance specifications for LoB, LoD, linearity, and precision were successfully verified. Both MAGLUMI HBeAg (CLIA) and MAGLUMI Anti-HBe (CLIA) assays exhibited satisfactory NPA and PPA (≥98%). No significant cross-reactivity or interference was observed. Furthermore, all tested plasma matrices demonstrated equivalence to serum in both assays. Conclusions: The MAGLUMI HBeAg (CLIA) and MAGLUMI Anti-HBe (CLIA) met the CLIS verification criteria with favorable analytical performance, and achieved high NPA and PPA relative to the Abbott Architect comparative assays. Besides, future concordance assessments based on a large intended cohort, together with independent clinical validation, are required to fully confirm their suitability for routine clinical application and management of HBV infection.
Ce résumé expose les affirmations des auteurs. BNTIC ne l’interprète pas comme une validation indépendante des résultats.
Le contrôle bibliographique ouvert
DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.
- Titre Crossref
- Analytical performance evaluation of MAGLUMI HBeAg and anti-HBe chemiluminescence immunoassays and comparison with the Abbott assays
- Date Crossref
- 19/08/2026
- Éditeur
- Frontiers Media SA
- Type
- journal-article
Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.
Où se fait cette recherche
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Shenzhen Blood Center pays non établi dans la noticeOrganisation à but non lucratif
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Jinan Central Hospital Medical Research and Laboratory Diagnostic Center pays non établi dans la noticeÉtablissement de santé
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Shandong First Medical University pays non établi dans la noticeUniversité ou école supérieure
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Ube (Japan) pays non établi dans la noticeEntreprise
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Blood Screening Department pays non établi dans la noticeInstitution
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Ltd. (Snibe) Shenzhen New Industries Biomedical Engineering Co. pays non établi dans la noticeEntreprise
Shenzhen Blood Center, Medical Research and Laboratory Diagnostic Center — Jinan Central Hospital et Shandong First Medical University, avec 3 autres affiliations.
Une affiliation ne permet pas de déduire la nationalité d’un auteur.