Evidence map›Paper›PMID 32472066›Full record

ArticleMucosal immunology2020

γδ T cells compose a developmentally regulated intrauterine population and protect against vaginal candidiasis.

L Monin, D S Ushakov, H Arnesen, N Bah, A Jandke, M Muñoz-Ruiz, J Carvalho, S Joseph, B C Almeida, M J Green and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Mucosal immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

36 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  4. Review
  5. Impact ofTropical medicine and infectious disease · 2025
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  6. mSphere · 2025
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  11. Review
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  13. ControllingInfection and immunity · 2024
    Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 6 institutions in 4 countries.

L MoninImmunoSurveillance Lab, The Francis Crick Institute, London, NW1 1AT, UK.ORCID http://orcid.org/0000-0002-4951-8105
D S UshakovImmunoSurveillance Lab, The Francis Crick Institute, London, NW1 1AT, UK.
H ArnesenFaculty of Veterinary Medicine, Norwegian University of Life Sciences (NMBU), N-0102, Oslo, Norway.
N BahBioinformatics and Biostatistics Team, The Francis Crick Institute, London, NW1 1AT, UK.
A JandkeImmunoSurveillance Lab, The Francis Crick Institute, London, NW1 1AT, UK.
M Muñoz-RuizImmunoSurveillance Lab, The Francis Crick Institute, London, NW1 1AT, UK.
J CarvalhoExperimental Histopathology Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
S JosephCentre for Host-Microbiome Interactions, Faculty of Dentistry, Oral & Craniofacial Sciences, Guy's Hospital, King's College London, London, SE1 9RT, UK.
B C AlmeidaExperimental Histopathology Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
M J GreenExperimental Histopathology Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
E NyeExperimental Histopathology Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
S HatanoDivision of Immunology and Genome Biology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Y YoshikaiDivision of Immunology and Genome Biology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
M CurtisCentre for Host-Microbiome Interactions, Faculty of Dentistry, Oral & Craniofacial Sciences, Guy's Hospital, King's College London, London, SE1 9RT, UK.
H CarlsenFaculty of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences (NMBU), 1432, Ås, Norway.
U SteinhoffInstitute for Medical Microbiology and Hospital Epidemiology, University of Marburg, 35037, Marburg, Germany.
P BoysenFaculty of Veterinary Medicine, Norwegian University of Life Sciences (NMBU), N-0102, Oslo, Norway.
A HaydayImmunoSurveillance Lab, The Francis Crick Institute, London, NW1 1AT, UK. adrian.hayday@kcl.ac.uk.
The Francis Crick Institute · GBNorwegian University of Life Sciences · NOGuy's Hospital · GBKing's College London · GBKyushu University · JPPhilipps University of Marburg · DE

Funding

Cancer Research UK FC001093Medical Research Council FC001093Medical Research Council MR/P012175/1Medical Research Council MR/P012175/2Wellcome Trust 106292/Z/14/ZWellcome Trust FC001093
6 · The paper itself

Abstract

This most comprehensive analysis to date of γδ T cells in the murine uterus reveals them to compose a unique local T-cell compartment. Consistent with earlier reports, most cells expressed a canonical Vγ6Vδ1 TCR, and produced interleukin (IL)-17A upon stimulation. Nonetheless, contrasting with earlier reports, uterine γδ T cells were not obviously intraepithelial, being more akin to sub-epithelial Vγ6Vδ1

Indexed as

AnimalsCandida albicansCandidiasisDisease ResistanceFemaleHumansInterferon-gammaMiceMice, Inbred C57BLMice, KnockoutNeutrophilsReceptors, Antigen, T-Cell, gamma-deltaT-LymphocytesUterusVaginaInterferon-gammaReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID32472066
PMCPMC7567646
OpenAlexW3029796166

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.