Evidence map›Paper›PMID 42200639›Full record

ArticleJournal of virology2026

Strain-specific differences in the response to egg-derived versus recombinant protein influenza vaccines.

Andrea N Loes, Rosario Araceli L Tarabi, Shuk Hang Li, Reilly K Atkinson, John Huddleston, Caroline Kikawa, Tachianna Griffiths, Elizabeth M Drapeau, Sook-San Wong, Samuel M S Cheng and 6 more

Abstract read
In one paragraph

Article in Journal of virology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Andrea N LoesHoward Hughes Medical Institute, Seattle, Washington, USA.
Rosario Araceli L TarabiDivision of Basic Sciences and Computational Biology Program, Fred Hutch Cancer Center, Seattle, Washington, USA.
Shuk Hang LiDepartment of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Reilly K AtkinsonDepartment of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
John HuddlestonVaccine and Infectious Disease Division, Fred Hutch Cancer Center, Seattle, Washington, USA.
Caroline KikawaDivision of Basic Sciences and Computational Biology Program, Fred Hutch Cancer Center, Seattle, Washington, USA.ORCID 0000-0002-8654-5663
Tachianna GriffithsDepartment of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Elizabeth M DrapeauDepartment of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Sook-San WongWorld Health Organization Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, The University of Hong Kong, Hong Kong, China.
Samuel M S ChengWorld Health Organization Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, The University of Hong Kong, Hong Kong, China.ORCID 0000-0001-7293-2331
Nancy H L LeungWorld Health Organization Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, The University of Hong Kong, Hong Kong, China.
Sarah CobeyDepartment of Ecology and Evolution, University of Chicago, Chicago, Illinois, USA.
Benjamin J CowlingWorld Health Organization Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, The University of Hong Kong, Hong Kong, China.ORCID 0000-0002-6297-7154
Trevor BedfordHoward Hughes Medical Institute, Seattle, Washington, USA.
Scott E HensleyDepartment of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.ORCID 0000-0002-2928-7506
Jesse D BloomHoward Hughes Medical Institute, Seattle, Washington, USA.ORCID 0000-0003-1267-3408

Funding

Howard Hughes Medical Institute InvestigatorNational Institute of Allergy and Infectious Diseases R01AI165821National Institute of Allergy and Infectious Diseases U01AI153700NIH HHS P30 CA015704 (RRID:SCR_022606), S10-OD-020069,S10-OD-028685ODCDC CDC HHS 75N93021C00015
6 · The paper itself

Abstract

The 2023/2024 influenza vaccine included an updated H1N1 component designed to better match a new clade of H1N1 that had multiple mutations in antigenic epitopes of hemagglutinin. Despite this update, the vaccine trended toward being less effective against the vaccine-matched H1N1 clade than the parental H1N1 clade lacking the new antigenic mutations. Here, we measure neutralization titers of serum antibodies from individuals who had received either a recombinant protein or an egg-derived vaccine against a set of viruses with hemagglutinins from 58 H1N1 strains representative of the diversity during the 2023/2024 season. We find that egg-derived vaccine recipients, but not recombinant protein vaccine recipients, had a relatively lower boost in neutralizing titers to the new clade that the updated vaccine was designed to target. We suggest that the difference in the extent that the egg-derived vs recombinant protein vaccines boosted neutralizing titers to the new H1N1 clade is because the seed strain for the egg-derived vaccine strain had acquired a reversion of a key antigenic mutation (K142R) present in that clade. Our results show how egg-derived vs recombinant protein vaccines can elicit different relative titer boosts against different subsets of viral strains, a phenomenon that could impact vaccine effectiveness. IMPORTANCE: Influenza vaccines can be produced from virus grown in eggs or grown in cells or made with recombinant protein. Egg-derived influenza vaccines often contain egg-adaptive mutations in the viral antigen hemagglutinin (HA) which can impact the antigenicity or immunogenicity of the HA. In this study, we compare neutralization titers from egg-derived and recombinant protein vaccine recipients against recently circulating influenza A(H1N1) strains. We find that the egg-derived vaccine induces less of a boost in titers than the recombinant protein vaccine to the new clade of viral strains that the vaccine was designed to target.

Indexed as

Influenza A Virus, H1N1 SubtypeInfluenza, HumanInfluenza VaccinesAnimalsAntibodies, NeutralizingAntibodies, ViralEggsHemagglutinin Glycoproteins, Influenza VirusHumansNeutralization TestsProtein Subunit VaccinesRecombinant ProteinsVaccines, SyntheticAntibodies, NeutralizingAntibodies, ViralHemagglutinin Glycoproteins, Influenza VirusInfluenza VaccinesProtein Subunit VaccinesRecombinant ProteinsVaccines, Syntheticegg adaptationhemagglutinininfluenzainfluenza vaccinepdmH1N1sequencing-based neutralization assay

Identifiers

PMID42200639
PMCPMC13288920

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.