Evidence map›Paper›PMID 34050027›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

A liposome-displayed hemagglutinin vaccine platform protects mice and ferrets from heterologous influenza virus challenge.

Zachary R Sia, Xuedan He, Ali Zhang, Jann C Ang, Shuai Shao, Amal Seffouh, Wei-Chiao Huang, Michael R D'Agostino, Amir Teimouri Dereshgi, Sambhara Suryaprakash and 5 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.6field-weighted citation impact, top 6% 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.

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

22 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  5. Broadly active intranasal influenza vaccine with a nanocomplex particulate adjuvant targeting mast cells and toll-like receptor 9.Journal of controlled release : official journal of the Controlled Release Society · 2025
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  19. Materials-based vaccines for infectious diseases.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2022
    Review
  20. 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

15 authors at 7 institutions in 3 countries.

Zachary R SiaDepartment of Biomedical Engineering, State University of New York at Buffalo, Buffalo, NY 14260.
Xuedan HeDepartment of Biomedical Engineering, State University of New York at Buffalo, Buffalo, NY 14260.
Ali ZhangMichael G. DeGroote Institute for Infectious Disease Research, McMaster Immunology Research Centre, Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4L8, Canada.
Jann C AngMichael G. DeGroote Institute for Infectious Disease Research, McMaster Immunology Research Centre, Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4L8, Canada.
Shuai ShaoDepartment of Biomedical Engineering, State University of New York at Buffalo, Buffalo, NY 14260.ORCID 0000-0002-2682-1830
Amal SeffouhDepartment of Anatomy and Cell Biology, McGill University, Montreal, QC H3A 0C7, Canada.
Wei-Chiao HuangDepartment of Biomedical Engineering, State University of New York at Buffalo, Buffalo, NY 14260.
Michael R D'AgostinoMichael G. DeGroote Institute for Infectious Disease Research, McMaster Immunology Research Centre, Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4L8, Canada.
Amir Teimouri DereshgiVeterans Administration Western New York Healthcare System, Buffalo, NY 14215.ORCID 0000-0002-7094-0546
Sambhara SuryaprakashInfluenza Division, National Center for Immunization and Respiratory Diseases, Atlanta, GA 30329.ORCID 0000-0002-4715-5793
Joaquin OrtegaDepartment of Anatomy and Cell Biology, McGill University, Montreal, QC H3A 0C7, Canada.
Hanne AndersenBIOQUAL Inc., Rockville, MD 20850.
Matthew S MillerMichael G. DeGroote Institute for Infectious Disease Research, McMaster Immunology Research Centre, Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4L8, Canada; mmiller@mcmaster.ca bdavidso@buffalo.edu jflovell@buffalo.edu.ORCID 0000-0003-3426-5069
Bruce A DavidsonVeterans Administration Western New York Healthcare System, Buffalo, NY 14215; mmiller@mcmaster.ca bdavidso@buffalo.edu jflovell@buffalo.edu.ORCID 0000-0001-8223-1870
Jonathan F LovellDepartment of Biomedical Engineering, State University of New York at Buffalo, Buffalo, NY 14260; mmiller@mcmaster.ca bdavidso@buffalo.edu jflovell@buffalo.edu.ORCID 0000-0002-9052-884X
McMaster University Medical Centre · CAUniversity at Buffalo, State University of New York · USMcGill University · CAVA Western New York Healthcare System · USBioqual · USFirst Affiliated Hospital of Zhengzhou University · CNNational Center for Immunization and Respiratory Diseases · US

Funding

Immunotherapy for acute lung injury secondary to influenzaR01HL151498 · NHLBI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI KNIGHT III, PAUL R · 2020 to 2023
$1.7M
An adjuvanted influenza vaccine platform for dose sparing, multiplexing, and rapid deploymentR41AI149954 · NIAID · POP BIOTECHNOLOGIES, INC · PI DAVIDSON, BRUCE A., KUTSCHER, HILLIARD · 2020 to 2020
$224k
CIHRNHLBI NIH HHS R01 HL151498NIAID NIH HHS HHSN272201700015CNIAID NIH HHS R41 AI149954
6 · The paper itself

Abstract

Recombinant influenza virus vaccines based on hemagglutinin (HA) hold the potential to accelerate production timelines and improve efficacy relative to traditional egg-based platforms. Here, we assess a vaccine adjuvant system comprised of immunogenic liposomes that spontaneously convert soluble antigens into a particle format, displayed on the bilayer surface. When trimeric H3 HA was presented on liposomes, antigen delivery to macrophages was improved in vitro, and strong functional antibody responses were induced following intramuscular immunization of mice. Protection was conferred against challenge with a heterologous strain of H3N2 virus, and naive mice were also protected following passive serum transfer. When admixed with the particle-forming liposomes, immunization reduced viral infection severity at vaccine doses as low as 2 ng HA, highlighting dose-sparing potential. In ferrets, immunization induced neutralizing antibodies that reduced the upper respiratory viral load upon challenge with a more modern, heterologous H3N2 viral strain. To demonstrate the flexibility and modular nature of the liposome system, 10 recombinant surface antigens representing distinct influenza virus strains were bound simultaneously to generate a highly multivalent protein particle that with 5 ng individual antigen dosing induced antibodies in mice that specifically recognized the constituent immunogens and conferred protection against heterologous H5N1 influenza virus challenge. Taken together, these results show that stable presentation of recombinant HA on immunogenic liposome surfaces in an arrayed fashion enhances functional immune responses and warrants further attention for the development of broadly protective influenza virus vaccines.

Indexed as

LiposomesAdjuvants, ImmunologicAnimalsAntibodies, NeutralizingAntibodies, ViralAntigens, ViralDose-Response Relationship, ImmunologicFerretsHemagglutinin Glycoproteins, Influenza VirusInfluenza A Virus, H3N2 SubtypeInfluenza A Virus, H5N1 SubtypeInfluenza VaccinesMiceAdjuvants, ImmunologicAntibodies, NeutralizingAntibodies, ViralAntigens, ViralHemagglutinin Glycoproteins, Influenza VirusInfluenza VaccinesLiposomesadjuvantcobalt porphyrininfluenza vaccineliposomesnanoparticle vaccine

Identifiers

PMID34050027
PMCPMC8179143
OpenAlexW3164780480

What OpenQuestion holds

Textmetadata
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.