Evidence map›Paper›PMID 41727041›Full record

ArticlebioRxiv : the preprint server for biology2026

Emergence and antigenic characterisation of influenza A(H3N2) viruses with hemagglutinin substitutions N158K and K189R during the 2024/25 influenza season.

Björn Koel, Alexander Mp Byrne, Sam Turner, Sarah James, Ruth Harvey, Monica Galiano, Christine Carr, Pascal Lexmond, Mark Pronk, Ruonan Liang and 7 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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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0citing papers 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

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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

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5 · Who and what money

Authors and funding

17 authors.

Björn KoelDepartment of Viroscience, Erasmus Medical Center, Rotterdam, the Netherlands.
Alexander Mp ByrneWHO Collaborating Centre for Reference and Research on Influenza, Worldwide Influenza Centre, the Francis Crick Institute, London, United Kingdom.
Sam TurnerCenter for Pathogen Evolution, University of Cambridge, Cambridge, United Kingdom.
Sarah JamesCenter for Pathogen Evolution, University of Cambridge, Cambridge, United Kingdom.
Ruth HarveyWHO Collaborating Centre for Reference and Research on Influenza, Worldwide Influenza Centre, the Francis Crick Institute, London, United Kingdom.
Monica GalianoWHO Collaborating Centre for Reference and Research on Influenza, Worldwide Influenza Centre, the Francis Crick Institute, London, United Kingdom.
Christine CarrWHO Collaborating Centre for Reference and Research on Influenza, Worldwide Influenza Centre, the Francis Crick Institute, London, United Kingdom.
Pascal LexmondDepartment of Viroscience, Erasmus Medical Center, Rotterdam, the Netherlands.
Mark PronkDepartment of Viroscience, Erasmus Medical Center, Rotterdam, the Netherlands.
Ruonan LiangDepartment of Chemical Biology & Drug Discovery, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, the Netherlands.
Geert-Jan BoonsDepartment of Chemical Biology & Drug Discovery, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, the Netherlands.
Robert P de VriesDepartment of Chemical Biology & Drug Discovery, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, the Netherlands.ORCID 0000-0002-1586-4464
Dirk EgginkCentre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, the Netherlands.
Nicola LewisWHO Collaborating Centre for Reference and Research on Influenza, Worldwide Influenza Centre, the Francis Crick Institute, London, United Kingdom.
Derek SmithCenter for Pathogen Evolution, University of Cambridge, Cambridge, United Kingdom.
Adam MeijerCentre for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, the Netherlands.ORCID 0000-0001-8074-7582
Ron FouchierDepartment of Viroscience, Erasmus Medical Center, Rotterdam, the Netherlands.

Funding

Automated chemo-enzymatic synthesis of N-glycans for host-pathogen interactionsR01AI165692 · NIAID · UNIVERSITY OF GEORGIA · PI BOONS, GEERT-JAN · 2022 to 2025
$2.2M
NIAID NIH HHS R01 AI165692Wellcome Trust CC1114
6 · The paper itself

Abstract

Background: Seasonal human influenza viruses can escape from antibody-mediated neutralization when amino acid changes occur in the hemagglutinin protein. Routine surveillance identified circulation of an A(H3N2) virus variant in the Netherlands with amino acid substitutions at hemagglutinin positions 158 and 189. These amino acid positions were previously responsible for antigenic change of influenza A(H3N2) viruses and potentially lead to escape of this variant from vaccine-mediated immunity. Aim: To characterize the emergence and antigenic properties of N158K and K189R double substitution virus variants. Methods: We analyzed the geographical and temporal dynamics of the double-substitution variant using a phylogeographic approach and used hemagglutination inhibition assays and antigenic cartography methods to map its antigenic properties. Results: A(H3N2) viruses carrying K189R were first detected in Guatemala in June 2024, before subsequently gaining the N158K substitution, which was intially detected in Colombia in November 2024, followed by detection in the Netherlands in December 2024. However, detections within Europe remained almost entirely confined to the Netherlands. The proportion of viruses carrying the N158K and K189R substitutions increased to 16% - 24% per collection week of sequenced Dutch viruses during the peak of the epidemic of the 2024-2025 respiratory season. Antigenic characterization of viruses with N158K and K189R substitutions indicated that these are antigenically distinct from the A(H3N2) components of 2025-2026 Northern Hemisphere vaccines, showing 8-192-fold reduction in hemagglutination inhibition titers with antisera against the vaccine strain compared to antisera against the homologous virus. Conclusions: Influenza A(H3N2) viruses with N158K and K189R escaped recognition by antibodies raised against the 2024-2025 and 2025/2026 Northern Hemipshere vaccine strains in hemagglutination inhibition assays. These variants circulated widely in the Netherlands during the 2024-2025 influenza season, raising concerns about reduced vaccine-mediated protection if such variants would spread more broadly during 2025-2026 Northern Hemipshere season.

Identifiers

PMID41727041
PMCPMC12918802

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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.