Evidence map›Paper›PMID 39994168›Full record

SynthesisReviews in medical virology2025

Relative Efficacy, Effectiveness and Safety of Newer and/or Enhanced Seasonal Influenza Vaccines for the Prevention of Laboratory-Confirmed Influenza in Individuals Aged 18 years and Over: Update of a Systematic Review.

Mona Askar, Karam Adel Ali, Madeleine Batke, Timo Brugger, Annika Falman, Anna Hayman Robertson, Jaime Jesús Pérez, Kari Johansen, Jorgen de Jonge, Tyra Grove Krause and 16 more

Erratum issuedAbstract readSystematic Review
In one paragraph

Synthesis in Reviews in medical virology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors.

Mona AskarImmunisation Unit, Robert Koch Institute, Berlin, Germany.
Karam Adel AliEuropean Centre for Disease Prevention and Control, Solna, Sweden.
Madeleine BatkeImmunisation Unit, Robert Koch Institute, Berlin, Germany.
Timo BruggerFaculty of Medicine, Institute for Evidence in Medicine, Medical Center - University of Freiburg, University of Freiburg, Freiburg, Germany.
Annika FalmanImmunisation Unit, Robert Koch Institute, Berlin, Germany.ORCID 0009-0002-7176-0894
Anna Hayman RobertsonDivision of Infection Control, Norwegian Institute of Public Health, Oslo, Norway.
Jaime Jesús PérezGeneral Directorate of Public Health and Addictions, IMIB-Arrixaca, Murcia University, Region of Murcia, Spain.
Kari JohansenPublic Health Agency of Sweden, Solna, Sweden.
Jorgen de JongeCenter for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven, The Netherlands.ORCID 0000-0003-3167-2435
Tyra Grove KrauseStatens Serum Institut, Copenhagen, Denmark.
Wiebe Külper-SchiekImmunisation Unit, Robert Koch Institute, Berlin, Germany.
Joerg J MeerpohlFaculty of Medicine, Institute for Evidence in Medicine, Medical Center - University of Freiburg, University of Freiburg, Freiburg, Germany.
Angeliki MelidouEuropean Centre for Disease Prevention and Control, Solna, Sweden.
Hanna NohynekFinnish Institute for Health and Welfare, Helsinki, Finland.
Carmen OlmedoVaccination Programme, General Directorate of Public Health, Ministry of Health, Madrid, Spain.
Kate OlssonEuropean Centre for Disease Prevention and Control, Solna, Sweden.
Ioanna PavlopoulouPediatric Research Laboratory, School of Health Sciences, Faculty of Nursing, National & Kapodistrian University of Athens, Goudi, Greece.
Vanessa PiechottaImmunisation Unit, Robert Koch Institute, Berlin, Germany.
Johanna RubinPublic Health Agency of Sweden, Solna, Sweden.
Johanna SchlabergImmunisation Unit, Robert Koch Institute, Berlin, Germany.
Christine SchmuckerFaculty of Medicine, Institute for Evidence in Medicine, Medical Center - University of Freiburg, University of Freiburg, Freiburg, Germany.
Waldemar SiemensFaculty of Medicine, Institute for Evidence in Medicine, Medical Center - University of Freiburg, University of Freiburg, Freiburg, Germany.
Jan StratilImmunisation Unit, Robert Koch Institute, Berlin, Germany.
Veronika UčakarCentre for Communicable Diseases, National Institute of Public Health, Ljubljana, Slovenia.
Ole WichmannImmunisation Unit, Robert Koch Institute, Berlin, Germany.
Thomas HarderImmunisation Unit, Robert Koch Institute, Berlin, Germany.ORCID 0009-0004-8659-220X

Funding

European Health and Digital Executive Agency
6 · The paper itself

Abstract

We performed an update (last search: 24 July 2023) of a systematic review on relative efficacy/effectiveness (rVE) and safety of newer/enhanced seasonal influenza vaccines in comparison with standard influenza vaccine or in head-to-head comparison. Eligible studies investigated adults aged ≥ 18 years, analysed the MF59-adjuvanted or high-dose or cell-based or recombinant or mRNA-based influenza vaccine and reported rVE or safety in randomised controlled trials (RCT) or non-randomised studies of interventions (NRSI). Of 1561 new entries identified, 17 studies were included. Together with 42 studies identified in the previous primary review they added up to 59 studies, all comparing newer/enhanced with standard seasonal influenza vaccines. Relative VE against laboratory-confirmed influenza was -30% (95%CI: -146% to 31%) to 88% (51%-100%; 7 NRSI) for the MF59-adjuvanted vaccine (low certainty of evidence, CoE); 24.2% (9.7%-36.5%; 1 RCT) and -9% (-158% to 54%) to 19% (-27% to 48%; 1 NRSI) for the high-dose vaccine (moderate CoE); -5.8% (-36.1% to 17.7%) to 21.4% (-7.3% to 42.4%; 2 NRSI) for the cell-based vaccine (low CoE); 30% (10%-47%; 1 RCT) and 3% (-31% to 28%) to 19% (-27% to 48%; 1 NRSI) for the recombinant vaccine (moderate CoE), respectively. Relative VE against laboratory-confirmed influenza-related hospitalisation was 59.2% (14.6%-80.5%; 1 NRSI) for the MF59-adjuvanted (moderate CoE); 27% (-1 to 48%; 1 NRSI) for the high-dose (low CoE); 8.5% (-75.9% to 52.3%; 1 NRSI) for the cell-based (low CoE); -7.3% (-52.1% to 24.4%) to 16.3% (-8.7% to 35.5%; 1 RCT) for the recombinant vaccine. No increased risk of serious adverse events was detected for any vaccine (12 RCT, 7 NRSI; low CoE). While all have a favourable safety profile, evidence on rVE of newer/enhanced vaccines is still limited, warranting further studies.

Indexed as

Influenza, HumanInfluenza VaccinesVaccine EfficacyAdjuvants, ImmunologicAdolescentAdultHumansPolysorbatesRandomized Controlled Trials as TopicSeasonsSqualeneYoung AdultAdjuvants, ImmunologicInfluenza VaccinesMF59 oil emulsionPolysorbatesSqualene

Identifiers

PMID39994168
PMCPMC11850296

What OpenQuestion holds

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Registered trials

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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.