Evidence map›Paper›PMID 42233155›Full record

ArticleFrontiers in cellular and infection microbiology2026

A novel multiplex approach for the comprehensive analysis of the Epstein-Barr virus-specific humoral immune response.

Carola Meindl, Ramona Weggel, Karolin Deichl, Kathrin Maria Fleischer, Paula Hofmeier, Mette Last, Julius Nückel, Elisa Planatscher, Lobna Ali Onsi, Anna Schütt and 2 more

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Carola MeindlChildren's Hospital, School of Medicine, Technische Universität München, Munich, Munich, Germany.
Ramona WeggelChildren's Hospital, School of Medicine, Technische Universität München, Munich, Munich, Germany.
Karolin DeichlChildren's Hospital, School of Medicine, Technische Universität München, Munich, Munich, Germany.
Kathrin Maria FleischerChildren's Hospital, School of Medicine, Technische Universität München, Munich, Munich, Germany.
Paula HofmeierInstitute of Virology, School of Medicine, Technische Universität München & Helmholtz Zentrum München, Munich, Germany.
Mette LastChildren's Hospital, School of Medicine, Technische Universität München, Munich, Munich, Germany.
Julius NückelChildren's Hospital, School of Medicine, Technische Universität München, Munich, Munich, Germany.
Elisa PlanatscherChildren's Hospital, School of Medicine, Technische Universität München, Munich, Munich, Germany.
Lobna Ali OnsiInstitute of Virology, School of Medicine, Technische Universität München & Helmholtz Zentrum München, Munich, Germany.
Anna SchüttChildren's Hospital, School of Medicine, Technische Universität München, Munich, Munich, Germany.
Uta BehrendsChildren's Hospital, School of Medicine, Technische Universität München, Munich, Munich, Germany.
Josef MautnerChildren's Hospital, School of Medicine, Technische Universität München, Munich, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The Epstein-Barr virus (EBV) is an oncogenic herpesvirus that establishes lifelong infections in more than 90% of the human population. EBV infection is typically diagnosed using serological assays, which also distinguish between acute and persistent infection. However, current diagnostic approaches rely on a limited set of viral proteins and may therefore fail to detect disease-specific antibody signatures associated with EBV-related cancers or autoimmune diseases. Comprehensive profiling of humoral responses against the complete EBV proteome could improve the sensitivity and specificity of serological diagnostics. Methods: We developed a serological multiplex assay covering all EBV proteins expressed in human cells, enabling measurement of virus-specific IgM, IgG, and IgA responses. The assay was evaluated using sera from healthy EBV carriers and EBV-negative controls. Near-infrared detection was employed to support quantitative analysis across a broad dynamic range. Performance was benchmarked against commercially available serological assays. Results: The multiplex assay demonstrated a broad dynamic range with linear quantification across several orders of magnitude. Comparative evaluation showed that the assay achieved sensitivity and specificity comparable to established commercial tests while enabling comprehensive antibody profiling against the full EBV proteome. Conclusion: This multiplex serological platform provides a robust approach for comprehensive characterization of EBV-specific humoral immune responses. By extending antibody profiling beyond the limited antigen panels used in routine diagnostics, the assay may facilitate the identification of novel biomarkers for EBV-associated cancers and autoimmune diseases. Future applications could contribute to improved diagnostic accuracy and support the development of targeted therapeutic strategies.

Indexed as

Antibodies, ViralEpstein-Barr Virus InfectionsHerpesvirus 4, HumanImmunity, HumoralSerologic TestsHumansImmunoglobulin AImmunoglobulin GImmunoglobulin MSensitivity and SpecificityViral ProteinsAntibodies, ViralImmunoglobulin AImmunoglobulin GImmunoglobulin MViral Proteinsantigen arraydiagnosticsEpstein-Barr virusimmunoglobulinmultiplex serology

Identifiers

PMID42233155
PMCPMC13223017

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.