Evidence map›Paper›PMID 41873331›Full record

ArticleDiscovery immunology2026

Porcine influenza mAbs to H3, H5, and H7 hemagglutinins recognize H3 egg adapted site and target the HA stem.

Tiphaine Cayol, Sonia Villanueva-Hernández, Emily Briggs, Charlotte May, Adam McNee, Ashutosh Vats, Bharti Mittal, Jean-Remy Sadeyen, Munir Iqbal, Danish Munir and 6 more

Abstract read
In one paragraph

Article in Discovery immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Tiphaine CayolHost Response, The Pirbright Institute, Woking, UK.
Sonia Villanueva-HernándezHost Response, The Pirbright Institute, Woking, UK.
Emily BriggsHost Response, The Pirbright Institute, Woking, UK.
Charlotte MayHost Response, The Pirbright Institute, Woking, UK.
Adam McNeeHost Response, The Pirbright Institute, Woking, UK.
Ashutosh VatsHost Response, The Pirbright Institute, Woking, UK.
Bharti MittalHost Response, The Pirbright Institute, Woking, UK.
Jean-Remy SadeyenHost Response, The Pirbright Institute, Woking, UK.
Munir IqbalHost Response, The Pirbright Institute, Woking, UK.
Danish MunirHost Response, The Pirbright Institute, Woking, UK.
Marie Di PlacidoHost Response, The Pirbright Institute, Woking, UK.
John A HammondHost Response, The Pirbright Institute, Woking, UK.
Alain TownsendChinese Academy of Medical Science Oxford Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Pramila RijalChinese Academy of Medical Science Oxford Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Basudev PaudyalHost Response, The Pirbright Institute, Woking, UK.ORCID https://orcid.org/0000-0001-6068-019X
Elma TchilianHost Response, The Pirbright Institute, Woking, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Monoclonal antibodies (mAbs) are critical tools for elucidating viral evolution, informing vaccine design, and developing antiviral therapeutics. Large-animal models, such as the pig, that closely mirror human immune responses are essential for understanding influenza immunity. Methods: Pigs were either infected or sequentially immunized with influenza viruses and monoclonal antibodies directed against H3, H5, and H7 influenza virus haemagglutinins were isolated. Antibody specificity, breadth, epitope targeting (head versus stem), neutralizing capacity, and Fc-mediated activity were assessed across influenza subtypes. Results: Pigs generated both strain-specific and broadly reactive mAbs targeting haemagglutinin head and stem epitopes. An H3-specific mAb (H3-57) selectively recognized the egg-adapted L194P mutation associated with reduced human vaccine effectiveness. H5 and H7 immunization induced neutralizing antibodies, including cross-group stem mAbs reactive with H1, H3, and H5 haemagglutinins. Fc-mediated activity correlated with antibody binding strength rather than epitope location. Conclusions: These findings demonstrate that pigs mount antibody responses closely resembling those observed in humans, including recognition of conserved stem epitopes and adaptive head mutations. Porcine mAbs represent powerful new tools for dissecting influenza immunity, guiding vaccine design, and enhancing pandemic preparedness using a physiologically relevant large-animal model.

Indexed as

H3H3 egg adaptation H3N2H5H7pig monoclonal antibodiesstem influenza antibodies

Identifiers

PMID41873331
PMCPMC13006140

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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.