Evidence map›Paper›PMID 42655661›Full record

ArticleViruses2026

FluEvoFormer: A Structure-Guided Generative Foundation Model for Prospective Influenza Antigenic Evolution and Vaccine Strain Selection.

Pankaj Agarwal, Sumendra Yogarayan, Md Shohel Sayeed

Abstract read
In one paragraph

Article in Viruses, 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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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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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

3 authors.

Pankaj AgarwalCentre for Intelligent Cloud Computing, COE for Advanced Cloud, Multimedia University, Melaka 75450, Malaysia.ORCID 0000-0002-1027-2419
Sumendra YogarayanCentre for Intelligent Cloud Computing, COE for Advanced Cloud, Multimedia University, Melaka 75450, Malaysia.ORCID 0000-0002-5151-2300
Md Shohel SayeedCentre for Intelligent Cloud Computing, COE for Advanced Cloud, Multimedia University, Melaka 75450, Malaysia.ORCID 0000-0002-0052-4870

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Seasonal influenza vaccine strain selection remains challenging because circulating viruses may drift after vaccine recommendations are made. This study presents FluEvoFormer, a structure-guided generative foundation model for prospective influenza antigenic evolution forecasting and vaccine strain ranking. The framework jointly encodes hemagglutinin and neuraminidase sequences and incorporates residue-contact graphs. Separate prediction heads estimate future viral dominance and the vaccine-virus antigenic match. Controlled future-like variant stress testing, uncertainty adjustments, and clade balancing are then used to rank vaccine candidates. A rolling retrospective evaluation was performed for target seasons involving the influenza A(H1N1)pdm09 virus and influenza A(H3N2) virus. The evaluation used cutoff-restricted sequence records, hemagglutination inhibition data, vaccine-composition records, protein-structure resources, and vaccine-effectiveness indicators. The historical training corpus for the influenza A(H1N1) virus also contained pre-2009 seasonal records. FluEvoFormer achieved the lowest held-out antigenicity prediction error, with mean absolute error (MAE) values of 0.389 for the combined historical influenza A(H1N1) virus corpus and 0.456 for the influenza A(H3N2) virus corpus. It also improved the future dominance prediction, with Kullback-Leibler (KL) divergence values of 0.255 and 0.289, respectively. The model selected candidates with higher empirical normalized coverage scores in seven out of 10 influenza A(H1N1)pdm09 virus seasons and nine out of 10 influenza A(H3N2) virus seasons. The predicted coverage score showed a strong positive correlation with external vaccine-effectiveness estimates. These findings support FluEvoFormer as a computational decision-support framework for prioritizing influenza vaccine candidates before downstream laboratory and public health evaluations.

Indexed as

Antigens, ViralEvolution, MolecularInfluenza A Virus, H1N1 SubtypeInfluenza, HumanInfluenza VaccinesHemagglutinin Glycoproteins, Influenza VirusHumansInfluenza A Virus, H3N2 SubtypeNeuraminidaseAntigens, ViralHemagglutinin Glycoproteins, Influenza VirusInfluenza VaccinesNeuraminidaseantigenic evolutiongenerative AIgraph transformerhemagglutinininfluenza vaccine strain selectionneuraminidaseprotein language modelvaccine candidate ranking

Identifiers

PMID42655661
PMCPMC13517461

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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.