Evidence map›Paper›PMID 32787280›Full record

ReviewMolecular pharmaceutics2021

Engineered Nanoparticle Applications for Recombinant Influenza Vaccines.

Zachary R Sia, Matthew S Miller, Jonathan F Lovell

Open access · greenAbstract readReview
In one paragraph

Review in Molecular pharmaceutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Intranasal Multiepitope PD-L1-siRNA-Based Nanovaccine: The Next-Gen COVID-19 Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. A liposome-displayed hemagglutinin vaccine platform protects mice and ferrets from heterologous influenza virus challenge.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  15. Intranasal vaccination with influenza HA/GO-PEI nanoparticles provides immune protection against homo- and heterologous strains.Proceedings of the National Academy of Sciences of the United States of America · 2021
    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

3 authors at 2 institutions in 2 countries.

Zachary R SiaDepartment of Biomedical Engineering, University at Buffalo, State University of New York, Buffalo, New York 14260, United States.
Matthew S MillerDepartment of Biochemistry and Biomedical Sciences, Michael G. DeGroote Institute for Infectious Diseases Research, McMaster Immunology Research Centre, McMaster University, Hamilton, Ontario L8S 4L8, Canada.
Jonathan F LovellDepartment of Biomedical Engineering, University at Buffalo, State University of New York, Buffalo, New York 14260, United States.ORCID 0000-0002-9052-884X
University at Buffalo, State University of New York · USMcMaster University Medical Centre · CA

Funding

Rationally-Designed, Spontaneous-Particleized Pfs48/45 for a Multivalent Malaria VaccineR01AI148557 · NIAID · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI JULIEN, JEAN-PHILIPPE, LOVELL, JONATHAN F · 2020 to 2024
$2.1M
Targeting Tumors with Resealable Nanovesicles Permeabilized by NIR LightDP5OD017898 · OD · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI LOVELL, JONATHAN F · 2013 to 2017
$1.9M
A His-tag Binding Membrane System for Generating Neutralizing Gp41 MPER antibodiesR21AI122964 · NIAID · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI LOVELL, JONATHAN F · 2016 to 2017
$436k
NIAID NIH HHS R01 AI148557NIAID NIH HHS R21 AI122964NIH HHS DP5 OD017898
6 · The paper itself

Abstract

Influenza viruses cause seasonal epidemics and represent a pandemic risk. With current vaccine methods struggling to protect populations against emerging strains, there is a demand for a next-generation flu vaccine capable of providing broad protection. Recombinant biotechnology, combined with nanomedicine techniques, could address this demand by increasing immunogenicity and directing immune responses toward conserved antigenic targets on the virus. Various nanoparticle candidates have been tested for use in vaccines, including virus-like particles, protein and carbohydrate nanoconstructs, antigen-carrying lipid particles, and synthetic and inorganic particles modified for antigen presentation. These methods have yielded some promising results, including protection in animal models against antigenically distinct influenza strains, production of antibodies with broad reactivity, and activation of potent T cell responses. Based on the evidence of current research, it is feasible that the next generation of influenza vaccines will combine recombinant antigens with nanoparticle carriers.

Indexed as

AnimalsAntigens, ViralDisease Models, AnimalDrug CarriersHumansImmunogenicity, VaccineInfluenza A virusInfluenza, HumanInfluenza VaccinesNanoparticlesProtein EngineeringRecombinant ProteinsVaccines, SyntheticViral ProteinsAntigens, ViralDrug CarriersInfluenza VaccinesRecombinant ProteinsVaccines, SyntheticViral Proteinsantigensinfluenzananoparticlesparticlesvaccine

Identifiers

PMID32787280
PMCPMC8011859
OpenAlexW3046343760

What OpenQuestion holds

Textmetadata
LicenceTDM
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.