Evidence map›Paper›PMID 23698367›Full record

ArticleNature2013

Self-assembling influenza nanoparticle vaccines elicit broadly neutralizing H1N1 antibodies.

Masaru Kanekiyo, Chih-Jen Wei, Hadi M Yassine, Patrick M McTamney, Jeffrey C Boyington, James R R Whittle, Srinivas S Rao, Wing-Pui Kong, Lingshu Wang, Gary J Nabel

4 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in Nature, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 513 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
513citing papers in PubMed, 1 pooled it
29.5field-weighted citation impact, top 1% of its field
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.

NCT03186781 phase1completednot on this mapstarted 2017, after this paper: background citation

VRC 316: A Phase I Open-Label Clinical Trial To Evaluate Dose, Safety, Tolerability, And Immunogenicity Of An Influenza HA Ferritin Vaccine, Alone Or In Prime-Boost Regimens With An Influenza DNA Vaccine In Healthy Adults

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2017 to 2019Enrolled50ConditionsInfluenzaArmsVRC-FLUNPF081-00-VP (HA-F A/Sing), VRC-FLUDNA082-00-VP (DNA A/Sing)
NCT03814720 phase1completednot on this mapstarted 2019, after this paper: background citation

VRC 321: A Phase I Open-Label Clinical Trial to Evaluate Dose, Safety, Tolerability, and Immunogenicity of an Influenza H1 Stabilized Stem Ferritin Vaccine, VRCFLUNPF099-00-VP, in Healthy Adults

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2019 to 2021Enrolled52ConditionsInfluenza InfectionArmsVRC-FLUNPF099-00-VP (H1ssF_3928)
NCT04579250 phase1completednot on this mapstarted 2020, after this paper: background citation

VRC 323: A Phase I Open-Label Clinical Trial to Evaluate the Dose, Safety, Tolerability and Immunogenicity of an Influenza H10 Stabilized Stem Ferritin Vaccine, VRC-FLUNPF0103-00-VP, in Healthy Adults

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2020 to 2022Enrolled25ConditionsInfluenzaArmsVRC-FLUNPF0103-00-VP (H10ssF-6473)
NCT05968989 phase1completednot on this mapstarted 2023, after this paper: background citation

VRC 326 (001614): A Phase I Open-Label Clinical Trial to Evaluate the Safety, Tolerability, and Immunogenicity of a Mosaic Hexavalent Influenza Vaccine VRC-FLUMOS0116-00-VP (FluMos-v2) in Healthy Adults

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2023 to 2025Enrolled30ConditionsInfluenzaArmsVRC-FLUMOS0116-00-VP( FLUMos-v2)
3 · Its place in the literature

Who cites it

513 citing papers in PubMed, 1 synthesis or guideline pooled it, 888 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Anti-idiotypic antibodies as molecular mimics of conserved influenza hemagglutinin epitopes.Protein science : a publication of the Protein Society · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Stabilized mosaic hemagglutinin immunogens as novel universal influenza virus vaccines.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  16. Article
  17. Article
  18. Review
  19. Chemical reviews · 2026
    Review
  20. Review

453 more citing papers are in PubMed but not listed here.

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

10 authors at 3 institutions in 1 country.

Masaru KanekiyoVaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
Chih-Jen Wei
Hadi M Yassine
Patrick M McTamney
Jeffrey C Boyington
James R R Whittle
Srinivas S Rao
Wing-Pui Kong
Lingshu Wang
Gary J Nabel
National Institutes of Health · USNational Institute of Allergy and Infectious Diseases · USSanofi (United States) · US

Funding

Influenza Vaccine Research and DevelopmentZIAAI005003 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI KANEKIYO, MASARU · 2009 to 2025
$89.8M
Influenza Vaccine DevelopmentZ01AI005003 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI NABEL, GARY J · 2002 to 2008
$2.7M
Intramural NIH HHS Z01 AI005003Intramural NIH HHS Z99 AI999999Intramural NIH HHS ZIA AI005003
6 · The paper itself

Abstract

Influenza viruses pose a significant threat to the public and are a burden on global health systems. Each year, influenza vaccines must be rapidly produced to match circulating viruses, a process constrained by dated technology and vulnerable to unexpected strains emerging from humans and animal reservoirs. Here we use knowledge of protein structure to design self-assembling nanoparticles that elicit broader and more potent immunity than traditional influenza vaccines. The viral haemagglutinin was genetically fused to ferritin, a protein that naturally forms nanoparticles composed of 24 identical polypeptides. Haemagglutinin was inserted at the interface of adjacent subunits so that it spontaneously assembled and generated eight trimeric viral spikes on its surface. Immunization with this influenza nanoparticle vaccine elicited haemagglutination inhibition antibody titres more than tenfold higher than those from the licensed inactivated vaccine. Furthermore, it elicited neutralizing antibodies to two highly conserved vulnerable haemagglutinin structures that are targets of universal vaccines: the stem and the receptor binding site on the head. Antibodies elicited by a 1999 haemagglutinin-nanoparticle vaccine neutralized H1N1 viruses from 1934 to 2007 and protected ferrets from an unmatched 2007 H1N1 virus challenge. This structure-based, self-assembling synthetic nanoparticle vaccine improves the potency and breadth of influenza virus immunity, and it provides a foundation for building broader vaccine protection against emerging influenza viruses and other pathogens.

Indexed as

AnimalsAntibodies, NeutralizingAntibodies, ViralBinding SitesCross ReactionsFemaleFerretsFerritinsHemagglutination Inhibition TestsHemagglutinin Glycoproteins, Influenza VirusInfluenza A Virus, H1N1 SubtypeInfluenza VaccinesMaleMiceMice, Inbred BALB CNanoparticlesAntibodies, NeutralizingAntibodies, ViralFerritinsHemagglutinin Glycoproteins, Influenza VirusInfluenza VaccinesVaccines, Inactivated

Identifiers

PMID23698367
PMCPMC8312026
OpenAlexW2002844537

What OpenQuestion holds

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Registered trials

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.