Evidence map›Paper›PMID 28584241›Full record

ArticleScientific reports2017

E. coli promotes human Vγ9Vδ2 T cell transition from cytokine-producing bactericidal effectors to professional phagocytic killers in a TCR-dependent manner.

M Barisa, A M Kramer, Y Majani, D Moulding, L Saraiva, M Bajaj-Elliott, J Anderson, K Gustafsson

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. Destabilisation of T cell-dependent humoral immunity in sepsis.Clinical science (London, England : 1979) · 2024
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Cell reports methods · 2022
    Article
  8. Article
  9. Review
  10. Review
  11. Unconventional T cells and kidney disease.Nature reviews. Nephrology · 2021
    Review
  12. Article
  13. Review
  14. Article
  15. Frontiers in immunology · 2020
    Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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.

M BarisaInfection, Immunity and Inflammation Program; UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1A 1EH, United Kingdom.ORCID 0000-0001-7846-6810
A M KramerInfection, Immunity and Inflammation Program; UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1A 1EH, United Kingdom.
Y MajaniDevelopmental Biology and Cancer Program, UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1A 1EH, United Kingdom.
D MouldingDevelopmental Biology and Cancer Program, UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1A 1EH, United Kingdom.
L SaraivaInfection, Immunity and Inflammation Program; UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1A 1EH, United Kingdom.ORCID 0000-0001-5642-5559
M Bajaj-ElliottInfection, Immunity and Inflammation Program; UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1A 1EH, United Kingdom. m.bajaj-elliott@ucl.ac.uk.
J AndersonDevelopmental Biology and Cancer Program, UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1A 1EH, United Kingdom. j.anderson@ucl.ac.uk.
K GustafssonInfection, Immunity and Inflammation Program; UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1A 1EH, United Kingdom. k.gustafsson@ucl.ac.uk.ORCID 0000-0002-5707-5543

Funding

Wellcome Trust
6 · The paper itself

Abstract

γδT cells provide immune-surveillance and host defense against infection and cancer. Surprisingly, functional details of γδT cell antimicrobial immunity to infection remain largely unexplored. Limited data suggests that γδT cells can phagocytose particles and act as professional antigen-presenting cells (pAPC). These potential functions, however, remain controversial. To better understand γδT cell-bacterial interactions, an ex vivo co-culture model of human peripheral blood mononuclear cell (PBMC) responses to Escherichia coli was employed. Vγ9Vδ2 cells underwent rapid T cell receptor (TCR)-dependent proliferation and functional transition from cytotoxic, inflammatory cytokine immunity, to cell expansion with diminished cytokine but increased costimulatory molecule expression, and capacity for professional phagocytosis. Phagocytosis was augmented by IgG opsonization, and inhibited by TCR-blockade, suggesting a licensing interaction involving the TCR and FcγR. Vγ9Vδ2 cells displayed potent cytotoxicity through TCR-dependent and independent mechanisms. We conclude that γδT cells transition from early inflammatory cytotoxic killers to myeloid-like APC in response to infectious stimuli.

Indexed as

B7-2 AntigenCytokinesEscherichia coliHLA-DR AntigensHumansImmunoglobulin GLymphocyte ActivationPhagocytesPhagocytosisPhenotypeReceptors, Antigen, T-Cell, gamma-deltaTh1 CellsT-LymphocytesZoledronic AcidB7-2 AntigenCytokinesHLA-DR AntigensImmunoglobulin GReceptors, Antigen, T-Cell, gamma-deltaZoledronic Acid

Identifiers

PMID28584241
PMCPMC5459831

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.