Evidence map›Paper›PMID 41021799›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Molecular divergence and convergence of mammalian antibody responses to the influenza virus hemagglutinin stem.

Huibin Lv, Qi Wen Teo, Tossapol Pholcharee, Wenkan Liu, Sawrab Roy, Lei Shi, Akshita B Gopal, Madison R Ardagh, Chunke Chen, Yuanxin Sun and 12 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

22 authors.

Huibin Lv *Department of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL 61801.
Qi Wen Teo *Department of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL 61801.
Tossapol Pholcharee *Department of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL 61801.ORCID 0000-0002-5347-1936
Wenkan Liu *Department of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL 61801.ORCID 0009-0002-1702-3148
Sawrab RoyDepartment of Veterinary Pathobiology, College of Veterinary Medicine, University of Missouri, Columbia, MO 65211.
Lei ShiDepartment of Veterinary Pathobiology, College of Veterinary Medicine, University of Missouri, Columbia, MO 65211.ORCID 0000-0003-2543-0042
Akshita B GopalDepartment of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL 61801.
Madison R ArdaghDepartment of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL 61801.
Chunke ChenThe Jockey Club School of Public Health and Primary Care, The Chinese University of Hong Kong, Hong Kong Special Administrative Region, China.
Yuanxin SunThe Jockey Club School of Public Health and Primary Care, The Chinese University of Hong Kong, Hong Kong Special Administrative Region, China.ORCID 0000-0003-2916-7763
Yang Wei HuanDepartment of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL 61801.
Walter N HarringtonDepartment of Host-Microbe Interactions, St. Jude Children's Research Hospital, Memphis, TN 38105.ORCID 0000-0003-3314-584X
Arjun MehtaDepartment of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL 61801.
Mateusz SzlembarskiDepartment of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL 61801.
Danbi ChoiDepartment of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL 61801.
Qihong GaoThe Jockey Club School of Public Health and Primary Care, The Chinese University of Hong Kong, Hong Kong Special Administrative Region, China.
Fiona S L FungThe Jockey Club School of Public Health and Primary Care, The Chinese University of Hong Kong, Hong Kong Special Administrative Region, China.
Fangxiu XuRoy J. Carver Biotechnology Center, University of Illinois Urbana-Champaign, Urbana, IL 61801.
Richard J WebbyDepartment of Host-Microbe Interactions, St. Jude Children's Research Hospital, Memphis, TN 38105.ORCID 0000-0002-4397-7132
Chris K P MokThe Jockey Club School of Public Health and Primary Care, The Chinese University of Hong Kong, Hong Kong Special Administrative Region, China.
Wenjun MaDepartment of Veterinary Pathobiology, College of Veterinary Medicine, University of Missouri, Columbia, MO 65211.ORCID 0000-0003-0395-9404
Nicholas C WuDepartment of Biochemistry, University of Illinois Urbana-Champaign, Urbana, IL 61801.ORCID 0000-0002-9078-6697

Funding

NIAID Centers of Excellence for Influenza Research and Response: Universal Influenza Vaccine Research Activities75N93021C00016 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI WEBBY, RICHARD · 2021 to 2025
$91.4M
Emerging key program of guangzhou laboratory, China EKPG22-30-6HHMI (HHMI) Emerging Pathogens InitiativeKinship Foundation (The Kinship Foundation) Searle Scholars ProgramNIAID NIH HHS 75N93021C00016Vallee Foundation (The Vallee Foundation) Vallee Scholars Program
6 · The paper itself

Abstract

Antibody responses to the influenza virus hemagglutinin (HA) stem, a major target for broadly protective vaccine development, have been extensively characterized in humans. However, they remain largely elusive in other natural influenza hosts, including pigs, which are considered intermediate hosts for the emergence of pandemic strains. By leveraging single-cell variable, diversity, and joining (VDJ) sequencing, this study identified 25 porcine antibodies to the HA stem, including two cross-group bnAbs, 14-8 and 15-1, from vaccinated specific-pathogen-free pigs and unvaccinated domestic pigs. Cryogenic electron microscopy analysis showed that 14-8 targeted the well-characterized central stem epitope, whereas 15-1 bound to a linear epitope spanning the HA1/HA2 junction. Additionally, while some porcine and human bnAbs targeted the central stem epitope via convergent molecular signatures, our results revealed a pig-specific recurring binding motif. Overall, our findings provide important insights into the commonalities and uniqueness of antibody responses between different species, which have significant implications for vaccine development for nonhuman animals.

Indexed as

Antibodies, ViralAntibody FormationHemagglutinin Glycoproteins, Influenza VirusInfluenza A virusAnimalsEpitopesHumansInfluenza VaccinesOrthomyxoviridae InfectionsSwineAntibodies, ViralEpitopesHemagglutinin Glycoproteins, Influenza VirusInfluenza Vaccinesbroadly neutralizing antibodiescryo-EMhemagglutinininfluenza viruspigs

Identifiers

PMID41021799
PMCPMC12519147

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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.