Evidence map›Paper›PMID 33603753›Full record

ArticleFrontiers in immunology2020

T-Bet Controls Cellularity of Intestinal Group 3 Innate Lymphoid Cells.

Jan-Hendrik Schroeder, Katrin Meissl, Dominika Hromadová, Jonathan W Lo, Joana F Neves, Jane K Howard, Helena Helmby, Nick Powell, Birgit Strobl, Graham M Lord

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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
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  6. Article
  7. Review
  8. ILC3: a case of conflicted identity.Frontiers in immunology · 2023
    Review
  9. Article
  10. Review
  11. Review
  12. Innate Lymphoid Cells and Intestinal Inflammatory Disorders.International journal of molecular sciences · 2022
    Review
  13. Review
  14. Article
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

10 authors at 4 institutions in 2 countries.

Jan-Hendrik SchroederSchool of Immunology and Microbial Sciences, King's College London, London, United Kingdom.
Katrin MeisslInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Dominika HromadováInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Jonathan W LoSchool of Immunology and Microbial Sciences, King's College London, London, United Kingdom.
Joana F NevesCentre for Host-Microbiome Interactions, King's College London, London, United Kingdom.
Jane K HowardDepartment of Diabetes, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College, London, United Kingdom.
Helena HelmbyDepartment of Infection Biology, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Nick PowellDivision of Digestive Diseases, Faculty of Medicine, Imperial College London, London, United Kingdom.
Birgit StroblInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Graham M LordSchool of Immunology and Microbial Sciences, King's College London, London, United Kingdom.
King's College London · GBUniversity of Veterinary Medicine Vienna · ATImperial College London · GBLondon School of Hygiene & Tropical Medicine · GB

Funding

Department of HealthMedical Research Council MR/K002996/1Medical Research Council MR/M003493/1Medical Research Council MR/R024812/1Wellcome Trust 091009Wellcome Trust WT101159
6 · The paper itself

Abstract

Innate lymphoid cells (ILC) play a significant immunological role at mucosal surfaces such as the intestine. T-bet-expressing group 1 innate lymphoid cells (ILC1) are believed to play a substantial role in inflammatory bowel disease (IBD). However, a role of T-bet-negative ILC3 in driving colitis has also been suggested in mouse models questioning T-bet as a critical factor for IBD. We report here that T-bet deficient mice had a greater cellularity of NKp46-negative ILC3 correlating with enhanced expression of RORγt and IL-7R, but independent of signaling through STAT1 or STAT4. We observed enhanced neutrophilia in the colonic lamina propria (cLP) of these animals, however, we did not detect a greater risk of T-bet-deficient mice to develop spontaneous colitis. Furthermore, by utilizing an

Indexed as

Immunity, InnateAnimalsColitisInflammatory Bowel DiseasesIntestinal MucosaLymphocytesMiceMice, KnockoutNuclear Receptor Subfamily 1, Group F, Member 3Receptors, Interleukin-7STAT1 Transcription FactorSTAT4 Transcription FactorT-bet Transcription FactorT-Box Domain ProteinsNuclear Receptor Subfamily 1, Group F, Member 3Receptors, Interleukin-7Rorc protein, mouseStat1 protein, mouseSTAT1 Transcription FactorStat4 protein, mouseSTAT4 Transcription FactorT-bet Transcription FactorT-Box Domain ProteinsILCsinnate lymphoid cellsintestinal inflammationmucosal homeostasisT-bet

Identifiers

PMID33603753
PMCPMC7884460
OpenAlexW3128878296

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.