Evidence map›Paper›PMID 39087764›Full record

ArticlemSphere2024

Lipid nanoparticle-encapsulated DNA vaccine confers protection against swine and human-origin H1N1 influenza viruses.

The N Nguyen, Danh C Lai, Sarah Sillman, Erika Petro-Turnquist, Eric A Weaver, Hiep L X Vu

Abstract read
In one paragraph

Article in mSphere, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 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

6 authors.

The N Nguyen *Nebraska Center for Virology, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.ORCID 0000-0003-0079-7358
Danh C Lai *Nebraska Center for Virology, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.ORCID 0000-0002-0584-2659
Sarah SillmanSchool of Veterinary Medicine and Biomedical Sciences and Nebraska Center for Virology, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
Erika Petro-TurnquistNebraska Center for Virology, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
Eric A WeaverNebraska Center for Virology, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
Hiep L X VuNebraska Center for Virology, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.ORCID 0000-0001-8084-4358

Funding

Rapid Manufacturing of a Universal Flu Vaccine Using TMV-conjugated Centralized AntigensR01AI147109 · NIAID · UNIVERSITY OF NEBRASKA LINCOLN · PI MCCORMICK, ALISON ANNE, WEAVER, ERIC A · 2020 to 2024
$3.2M
Comparative Virology Research Training ProgramT32AI125207 · NIAID · UNIVERSITY OF NEBRASKA LINCOLN · PI WEAVER, ERIC A · 2016 to 2020
$844k
NIAID NIH HHS R01 AI147109NIAID NIH HHS T32 AI125207U.S. Department of Agriculture (USDA) 1020750U.S. Department of Agriculture (USDA) 2020-67015-31414
6 · The paper itself

Abstract

In 2009, a novel swine-origin H1N1 virus emerged, causing a pandemic. The virus, known as H1N1pdm09, quickly displaced the circulating H1 lineage and became the dominant seasonal influenza A virus subtype infecting humans. Human-to-swine spillovers of the H1N1pdm09 have occurred frequently, and each occurrence has led to sustained transmission of the human-origin H1N1pdm09 within swine populations. In the present study, we developed a lipid nanoparticle-based DNA vaccine (LNP-DNA) containing the hemagglutinin gene of a swine-origin H1N1pdm09. In pigs, this LNP-DNA vaccine induced a robust antibody response after a single intramuscular immunization and protected the pigs against challenge infection with the homologous swine-origin H1N1pdm09 virus. In a mouse model, the LNP-DNA vaccine induced antibody and T-cell responses and protected mice against lethal challenge with a mouse-adapted human-origin H1N1pdm09 virus. These findings demonstrate the potential of the LNP-DNA vaccine to protect against both swine- and human-origin H1N1pdm09 viruses. IMPORTANCE: Swine influenza A virus (IAV) is widespread and causes significant economic losses to the swine industry. Moreover, bidirectional transmission of IAV between swine and humans commonly occurs. Once introduced into the swine population, human-origin IAV often reassorts with endemic swine IAV, resulting in reassortant viruses. Thus, it is imperative to develop a vaccine that is not only effective against IAV strains endemic in swine but also capable of preventing the spillover of human-origin IAV. In this study, we developed a lipid nanoparticle-encapsulated DNA plasmid vaccine (LNP-DNA) that demonstrates efficacy against both swine- and human-origin H1N1 viruses. The LNP-DNA vaccines are non-infectious and non-viable, meeting the criteria to serve as a vaccine platform for rapidly updating vaccines. Collectively, this LNP-DNA vaccine approach holds great potential for alleviating the impact of IAV on the swine industry and preventing the emergence of reassortant IAV strains.

Indexed as

Antibodies, ViralInfluenza A Virus, H1N1 SubtypeInfluenza, HumanInfluenza VaccinesNanoparticlesOrthomyxoviridae InfectionsSwine DiseasesVaccines, DNAAnimalsFemaleHemagglutinin Glycoproteins, Influenza VirusHumansLiposomesMiceMice, Inbred BALB CSwineAntibodies, ViralHemagglutinin Glycoproteins, Influenza VirusInfluenza VaccinesLipid NanoparticlesLiposomesVaccines, DNADNA vaccineH1N1pdm09influenza A viruslipid nanoparticles

Identifiers

PMID39087764
PMCPMC11351038

What OpenQuestion holds

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LicenceCC BY
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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.