Evidence map›Paper›PMID 28057386›Full record

ArticleVaccine2017

Nanoparticles decorated with viral antigens are more immunogenic at low surface density.

Matthew G Brewer, Anthony DiPiazza, Joshua Acklin, Changyong Feng, Andrea J Sant, Stephen Dewhurst

Abstract read
In one paragraph

Article in Vaccine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Memory B cell development in response to mRNA SARS-CoV-2 and nanoparticle immunization in mice.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  2. Review
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  11. Protein Vaccination Directs the CD4Journal of virology · 2019
    Article
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  15. Review
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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 at 1 institution in 1 country.

Matthew G BrewerDepartment of Microbiology and Immunology, University of Rochester, Rochester, NY 14642, United States.
Anthony DiPiazzaDepartment of Microbiology and Immunology, University of Rochester, Rochester, NY 14642, United States; David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY 14642, United States.
Joshua AcklinDepartment of Microbiology and Immunology, University of Rochester, Rochester, NY 14642, United States.
Changyong FengDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, NY 14642, United States.
Andrea J SantDepartment of Microbiology and Immunology, University of Rochester, Rochester, NY 14642, United States; David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY 14642, United States.
Stephen DewhurstDepartment of Microbiology and Immunology, University of Rochester, Rochester, NY 14642, United States. Electronic address: stephen_dewhurst@urmc.rochester.edu.
University of Rochester · US

Funding

Virology/Immunology CoreP30AI078498 · NIAID · UNIVERSITY OF ROCHESTER · PI DEWHURST, STEPHEN · 2008 to 2018
$14.6M
The T32 Predoctoral Training Program in Immunology (PTPI)T32AI007285 · NIAID · UNIVERSITY OF ROCHESTER · PI Scott Andrew Gerber, JACQUES Robert · 1986 to 2026
$7.6M
Training in HIV Replication and PathogenesisT32AI049815 · NIAID · UNIVERSITY OF ROCHESTER · PI WEDEKIND, JOSEPH E · 2001 to 2020
$3.5M
NIAID NIH HHS P30 AI078498NIAID NIH HHS T32 AI007285NIAID NIH HHS T32 AI049815
6 · The paper itself

Abstract

There is an urgent need to develop protective vaccines for high priority viral pathogens. One approach known to enhance immune responses to viral proteins is to display them on a nanoparticle (NP) scaffold. However, little is known about the effect of protein density on the B cell response to antigens displayed on NPs. To address this question HIV-1 Envelope (Env) and influenza hemagglutinin (HA) were displayed on a polystyrene-based NP scaffold at various densities - corresponding to mean antigen distances that span the range encountered on naturally occurring virions. Our studies revealed that NPs displaying lower densities of Env or HA more efficiently stimulated antigen-specific B cells in vitro, as measured by calcium flux, than did NPs displaying higher antigen densities. Similarly, NPs displaying a low density of Env or HA also elicited higher titers of antigen-specific serum IgG in immunized BALB/c mice (including elevated titers of hemagglutination-inhibiting antibodies), as well as an increased frequency of antigen-specific antibody secreting cells in the lymph node, spleen and bone marrow. Importantly, our studies showed that the enhanced B cell response elicited by the lower density NPs is likely secondary to more efficient development of follicular helper CD4 T cells and germinal center B cells. These findings demonstrate that the density of antigen on a NP scaffold is a critical determinant of the humoral immune response elicited, and that high density display does not always result in an optimal response.

Indexed as

AdsorptionAnimalsAntibodies, ViralB-LymphocytesBone Marrow CellsCalciumenv Gene Products, Human Immunodeficiency VirusFemaleHemagglutinin Glycoproteins, Influenza VirusHIV-1HumansImmunizationInfluenza A virusLymph NodesMiceMice, Inbred BALB CAntibodies, ViralCalciumenv Gene Products, Human Immunodeficiency VirusHemagglutinin Glycoproteins, Influenza VirusPolystyrenesSolutionsAntigen densityAntigen displayEnvelopeHemagglutininHIVHumoral immunityInfluenzaNanoparticle

Identifiers

PMID28057386
PMCPMC5876043
OpenAlexW2568362831

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.