Evidence map›Paper›PMID 27039982›Full record

ReviewCurrent opinion in virology2016

Engineering virus-like particles as vaccine platforms.

Kathryn M Frietze, David S Peabody, Bryce Chackerian

Abstract readReview
In one paragraph

Review in Current opinion in virology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 136 papers.

0numbers the graph read from it
0cells of the map it votes in
136citing 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

136 citing papers in PubMed.

  1. Review
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  14. Unlocking Transplant Tolerance with Biomaterials.Advanced healthcare materials · 2025
    Review
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76 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

3 authors.

Kathryn M FrietzeDepartment of Molecular Genetics and Microbiology, School of Medicine, University of New Mexico, United States.
David S PeabodyDepartment of Molecular Genetics and Microbiology, School of Medicine, University of New Mexico, United States.
Bryce ChackerianDepartment of Molecular Genetics and Microbiology, School of Medicine, University of New Mexico, United States. Electronic address: bchackerian@salud.unm.edu.

Funding

RNA-BINDING SITE OF A TRANSLATIONAL REPRESSORR01GM042901 · NIGMS · UNIVERSITY OF NEW MEXICO · PI PEABODY, DAVID S. · 1991 to 2011
$2.7M
A VLP-based platform for Vaccine DiscoveryR01AI083305 · NIAID · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI CHACKERIAN, BRYCE C · 2010 to 2013
$1.2M
NIAID NIH HHS R01 AI083305NIGMS NIH HHS R01 GM042901
6 · The paper itself

Abstract

Virus-like particles (VLPs) have been utilized as vaccine platforms to increase the immunogenicity of heterologous antigens. A variety of diverse VLP types can serve as vaccine platforms, and research has focused on engineering VLPs to improve their efficacy as vaccines, enhance their stability, and allow for more versatile display of antigens. Here, we review selected VLP vaccine platforms, highlight efforts to improve these platforms through structure-informed rational design, and point to areas of future research that will assist in these efforts.

Indexed as

Immunogenicity, VaccineAntigens, ViralGenetic EngineeringVaccines, Virus-Like ParticleAntigens, ViralVaccines, Virus-Like Particle

Identifiers

PMID27039982
PMCPMC4983494

What OpenQuestion holds

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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.