Evidence map›Paper›PMID 28375554›Full record

ArticleImmunology2017

Inflammatory responses to influenza vaccination at the extremes of age.

Jacqueline U McDonald, Ziyun Zhong, Helen T Groves, John S Tregoning

Open access · greenAbstract read
In one paragraph

Article in Immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

  1. Immunology of RNA-based vaccines: The critical interplay between inflammation and expression.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
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  17. Acute phase protein response to viral infection and vaccination.Archives of biochemistry and biophysics · 2019
    Review
  18. Article
  19. Article
  20. Adjuvanted influenza vaccines.Human vaccines & immunotherapeutics · 2018
    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

4 authors at 1 institution in 1 country.

Jacqueline U McDonaldMucosal Infection and Immunity group, Section of Virology, Department of Medicine, Imperial College London, London, UK.
Ziyun ZhongMucosal Infection and Immunity group, Section of Virology, Department of Medicine, Imperial College London, London, UK.
Helen T GrovesMucosal Infection and Immunity group, Section of Virology, Department of Medicine, Imperial College London, London, UK.
John S TregoningMucosal Infection and Immunity group, Section of Virology, Department of Medicine, Imperial College London, London, UK.ORCID 0000-0001-8093-8741
Imperial College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Age affects the immune response to vaccination, with individuals at the extremes of age responding poorly. The initial inflammatory response to antigenic materials shapes the subsequent adaptive response and so understanding is required about the effect of age on the profile of acute inflammatory mediators. In this study we measured the local and systemic inflammatory response after influenza vaccination or infection in neonatal, young adult and aged mice. Mice were immunized intramuscularly with inactivated influenza vaccine with and without the adjuvant MF59 and then challenged with H1N1 influenza. Age was the major factor affecting the inflammatory profile after vaccination: neonatal mice had more interleukin-1α (IL-1α), C-reactive protein (CRP) and granulocyte-macrophage colony-stimulating factor (GMCSF), young adults more tumour necrosis factor-α (TNF), and elderly mice more interleukin-1 receptor antagonist (IL-1RA), IL-2RA and interferon-γ-induced protein 10 (IP10). Notably the addition of MF59 induced IL-5, granulocyte colony-stimulating factor (G-CSF), Keratinocyte Chemotractant (KC) and monocyte chemoattractant protein 1 (MCP1) in all ages of animals and levels of these cytokines correlated with antibody responses. Age also had an impact on the efficacy of vaccination: neonatal and young adult mice were protected against challenge, but aged mice were not. There were striking differences in the localization of the cytokine response depending on the route of exposure: vaccination led to a high serum response whereas intranasal infection led to a low serum response but a high lung response. In conclusion, we demonstrate that age affects the inflammatory response to both influenza vaccination and infection. These age-induced differences need to be considered when developing vaccination strategies for different age groups.

Indexed as

AgingAnimalsAnimals, NewbornAntibodies, ViralCytokinesHumansInflammation MediatorsInfluenza A Virus, H1N1 SubtypeInfluenza, HumanInfluenza VaccinesLungMiceOrthomyxoviridae InfectionsPolysorbatesSqualeneVaccinationAntibodies, ViralCytokinesInflammation MediatorsInfluenza VaccinesMF59 oil emulsionPolysorbatesSqualenecytokinelungmucosavaccinationviral

Identifiers

PMID28375554
PMCPMC5506419
OpenAlexW2605089515

What OpenQuestion holds

Textmetadata
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.