Evidence map›Paper›PMID 25203448›Full record

ArticleVaccine2014

The Split Virus Influenza Vaccine rapidly activates immune cells through Fcγ receptors.

William E O'Gorman, Huang Huang, Yu-Ling Wei, Kara L Davis, Michael D Leipold, Sean C Bendall, Brian A Kidd, Cornelia L Dekker, Holden T Maecker, Yueh-Hsiu Chien and 1 more

2 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in Vaccine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.6field-weighted citation impact, top 7% 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.

NCT03022422 phase4completednot on this map

Protective Mechanisms Against a Pandemic Respiratory Virus: B-Cell, T-cell, and General Immune Response to Seasonal Influenza Vaccine. Year 3, 2011

TypeinterventionalSponsorStanford UniversityRan2011 to 2011Enrolled63ConditionsInfluenzaArmsTIV, High-Dose TIV
NCT03022435 phase4completednot on this map

Protective Mechanisms Against a Pandemic Respiratory Virus: B-cell, T-cell, and General Immune Response to Seasonal Influenza Vaccine. Year 4, 2012

TypeinterventionalSponsorStanford UniversityRan2012 to 2013Enrolled22ConditionsInfluenzaArmsTIV, High-Dose TIV, LAIV
3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
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  15. Article
  16. Review
  17. An adjuvant-modulated vaccine response in human whole blood.Human vaccines & immunotherapeutics · 2017
    Article
  18. Article
  19. Heparin reduces nonspecific eosinophil staining artifacts in mass cytometry experiments.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2016
    Article
  20. Role of Immune Aging in Susceptibility to West Nile Virus.Methods in molecular biology (Clifton, N.J.) · 2016
    Review
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

11 authors at 1 institution in 1 country.

William E O'GormanThe Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305, United States.
Huang HuangThe Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305, United States.
Yu-Ling WeiThe Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305, United States.
Kara L DavisDepartment of Pediatrics, Stanford University, Stanford, CA 94305, United States.
Michael D LeipoldHuman Immune Monitoring Center, Stanford University, Stanford, CA 94305, United States; Institute for Immunity, Transplantation, and Infection, Stanford University, Stanford, CA 94305, United States.
Sean C BendallThe Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305, United States.
Brian A KiddInstitute for Immunity, Transplantation, and Infection, Stanford University, Stanford, CA 94305, United States.
Cornelia L DekkerDepartment of Pediatrics, Stanford University, Stanford, CA 94305, United States.
Holden T MaeckerHuman Immune Monitoring Center, Stanford University, Stanford, CA 94305, United States; Institute for Immunity, Transplantation, and Infection, Stanford University, Stanford, CA 94305, United States.
Yueh-Hsiu ChienThe Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305, United States.
Mark M DavisThe Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305, United States; Institute for Immunity, Transplantation, and Infection, Stanford University, Stanford, CA 94305, United States; Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, United States. Electronic address: mmdavis@stanford.edu.
Stanford University · US

Funding

Using a tonsil organoid system to probe conditions for the induction of protective antibody and T cell responses to influenza.U19AI057229 · NIAID · STANFORD UNIVERSITY · PI Mark Morris Davis · 2003 to 2026
$88.5M
MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
Vaccination and infection: indicators of immunological health and responsivenessU19AI090019 · NIAID · STANFORD UNIVERSITY · PI DAVIS, MARK MORRIS · 2010 to 2015
$17.3M
Howard Hughes Medical InstituteNIAID NIH HHS T32 AI007290NIAID NIH HHS T32-AI007290NIAID NIH HHS U19 AI057229NIAID NIH HHS U19-AI057229NIAID NIH HHS U19 AI090019NIAID NIH HHS U19-AI090019
6 · The paper itself

Abstract

Seasonal influenza vaccination is one of the most common medical procedures and yet the extent to which it activates the immune system beyond inducing antibody production is not well understood. In the United States, the most prevalent formulations of the vaccine consist of degraded or "split" viral particles distributed without any adjuvants. Based on previous reports we sought to determine whether the split influenza vaccine activates innate immune receptors-specifically Toll-like receptors. High-dimensional proteomic profiling of human whole-blood using Cytometry by Time-of-Flight (CyTOF) was used to compare signaling pathway activation and cytokine production between the split influenza vaccine and a prototypical TLR response ex vivo. This analysis revealed that the split vaccine rapidly and potently activates multiple immune cell types but yields a proteomic signature quite distinct from TLR activation. Importantly, vaccine induced activity was dependent upon the presence of human sera indicating that a serum factor was necessary for vaccine-dependent immune activation. We found this serum factor to be human antibodies specific for influenza proteins and therefore immediate immune activation by the split vaccine is immune-complex dependent. These studies demonstrate that influenza virus "splitting" inactivates any potential adjuvants endogenous to influenza, such as RNA, but in previously exposed individuals can elicit a potent immune response by facilitating the rapid formation of immune complexes.

Indexed as

AdultAntibodies, ViralCells, CulturedCytokinesFemaleGPI-Linked ProteinsHumansImmunoglobulin GInfluenza, HumanInfluenza VaccinesISCOMsMaleMonocytesReceptors, IgGSignal TransductionToll-Like Receptor 7Antibodies, ViralCytokinesFCGR3B protein, humanGPI-Linked ProteinsImmunoglobulin GInfluenza VaccinesISCOMsReceptors, IgGTLR7 protein, humanTLR8 protein, humanToll-Like Receptor 7Toll-Like Receptor 8Fcγ receptorsImmunologyInfluenzaMass cytometryVaccine

Identifiers

PMID25203448
PMCPMC4191649
OpenAlexW2054718729

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.