Evidence map›Paper›PMID 32117282›Full record

ArticleFrontiers in immunology2020

Natural Killer Cells Dampen the Pathogenic Features of Recall Responses to Influenza Infection.

Jason P Mooney, Tedi Qendro, Marianne Keith, Adrian W Philbey, Helen T Groves, John S Tregoning, Martin R Goodier, Eleanor M Riley

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Targeting natural killer cells to enhance vaccine responses.Trends in pharmacological sciences · 2021
    Review
  7. Review
  8. Frontiers in pharmacology · 2021
    Review
  9. 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

8 authors at 3 institutions in 1 country.

Jason P MooneyDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Tedi QendroDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Marianne KeithDivision of Infection and Immunity, The Roslin Institute, University of Edinburgh, Edinburgh, United Kingdom.
Adrian W PhilbeyEaster Bush Pathology, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh, United Kingdom.
Helen T GrovesDepartment of Medicine, Imperial College London, London, United Kingdom.
John S TregoningDepartment of Medicine, Imperial College London, London, United Kingdom.
Martin R GoodierDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Eleanor M RileyDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, United Kingdom.
University of Edinburgh · GBImperial College London · GBLondon School of Hygiene & Tropical Medicine · GB

Funding

Medical Research Council G1000808Medical Research Council MR/K501281/1
6 · The paper itself

Abstract

Despite evidence of augmented Natural Killer (NK) cell responses after influenza vaccination, the role of these cells in vaccine-induced immunity remains unclear. Here, we hypothesized that NK cells might increase viral clearance but possibly at the expense of increased severity of pathology. On the contrary, we found that NK cells serve a homeostatic role during influenza virus infection of vaccinated mice, allowing viral clearance with minimal pathology. Using a diphtheria toxin receptor transgenic mouse model, we were able to specifically deplete NKp46+ NK cells through the administration of diphtheria toxin. Using this model, we assessed the effect of NK cell depletion prior to influenza challenge in vaccinated and unvaccinated mice. NK-depleted, vaccinated animals lost significantly more weight after viral challenge than vaccinated NK intact animals, indicating that NK cells ameliorate disease in vaccinated animals. However, there was also a significant reduction in viral load in NK-depleted, unvaccinated animals indicating that NK cells also constrain viral clearance. Depletion of NK cells after vaccination, but 21 days before infection, did not affect viral clearance or weight loss-indicating that it is the presence of NK cells during the infection itself that promotes homeostasis. Further work is needed to identify the mechanism(s) by which NK cells regulate adaptive immunity in influenza-vaccinated animals to allow efficient and effective virus control whilst simultaneously minimizing inflammation and pathology.

Indexed as

AnimalsInfluenza VaccinesKiller Cells, NaturalMiceMice, Inbred C57BLOrthomyxoviridae InfectionsInfluenza Vaccinesdiphtheria toxininfluenzalungmiceNK cellvaccine

Identifiers

PMID32117282
PMCPMC7019041
OpenAlexW3004508173

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.