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Antigenic changes in influenza A(H3N2) driven by genetic evolution: Insights from virological surveillance, EU/EEA, week 40/2023 to week 9/2024

  • Eeva K. Broberg*
  • , Maja Vukovikj
  • , Olov Svartström
  • , the ERLI-Net network
  • , Iris Hasibra
  • , Maximilian Riess
  • *Corresponding author for this work
  • European Centre for Disease Prevention and Control
  • World Health Organization
  • National Influenza Center in Belgium
  • National Center of Infectious and Parasitic Diseases Bulgaria
  • Croatian National Institute of Public Health
  • Czech National Institute of Public Health
  • Statens Serum Institut
  • Health Board
  • National Institute for Health and Welfare
  • Institut Pasteur Paris
  • Hospices Civils de Lyon
  • Robert Koch-Institut
  • National Influenza Centre for Northern Greece
  • Institut Pasteur Helleniqe
  • Landspitali University Hospital
  • Istituto Superiore di Sanita
  • National Public Health Surveillance Laboratory (Vilnius)
  • Laboratoire National de Santé
  • Ministry for Health
  • Norwegian Institute of Public Health
  • National Medicines Institute, Warsaw
  • National Reference Laboratory for Influenza and Other Respiratory Viruses
  • Instituto Nacional de Saúde Doutor Ricardo Jorge
  • National Institute of Public Health - Romania
  • Slovak Academy of Sciences
  • Environment and Food

Research output: Contribution to journalArticleAcademicpeer-review

3 Citations (Scopus)
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Abstract

Background: During the 2023/24 influenza season in the European Union/European Economic Area (EU/ EEA), influenza viruses A(H1N1)pdm09, A(H3N2) and B/ Victoria viruses were co-circulating. Aim: We aimed to describe the circulating influenza viruses by (sub)type, genetic clade, antigenic group and antiviral susceptibility in that season in the EU/EEA. Methods: We collected surveillance data from EU/EEA countries through weekly submissions to The European Surveillance System (TESSy). Data were submitted in strain-based format for weeks 40/2023 to 9/2024. Results: Twenty-nine EU/EEA countries reported 154,718 influenza virus detections (primary care sentinel and non-sentinel combined), of which 97% (150,692) were type A and 3% (4,026) were type B. Of the subtyped influenza A viruses, 30,463 (75%) were influenza A(H1)pdm09 and 10,174 (25%) were influenza A(H3). For 809 (20%) of the type B viruses, the lineage was determined; all were B/Victoria/2/87 lineage, and none were B/ Yamagata/16/88 lineage. Genetic diversification of seasonal influenza viruses continued, and clade 5a.2a of A(H1N1)pdm09, 2a.3a.1 of A(H3N2) and V1A.3a.2 of B/Victoria-lineage viruses dominated. Of the A(H3N2) 2a.3a.1 viruses, 23% were antigenically distinct from the 2023/24 vaccine virus. Conclusion: The 2023/24 influenza season was characterised by co-circulation of different influenza (sub)types, antigenically similar to the components recommended for the 2023/24 northern hemisphere vaccine, A/Victoria/4897/2022 (egg-based) and A/Wisconsin/67/2022 (cell culture- or recombinant-based). However, genetic diversification of the viruses continued. The World Health Organization’s vaccine recommendations for the northern hemisphere 2024/25 season were updated to include a new A(H3N2) component, while maintaining the current A(H1N1)pdm09 and B/Victoria components.

Original languageEnglish
Article number2400395
JournalEurosurveillance
Volume29
Issue number50
DOIs
Publication statusPublished - 12 Dec 2024

Bibliographical note

Publisher Copyright:
© 2024 European Centre for Disease Prevention and Control (ECDC). All rights reserved.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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