Evidence map›Paper›PMID 30891037›Full record

ArticleFrontiers in immunology2019

Differential Effects of the Absence of Nkx2-3 and MAdCAM-1 on the Distribution of Intestinal Type 3 Innate Lymphoid Cells and Postnatal SILT Formation in Mice.

Dóra Vojkovics, Zoltán Kellermayer, Fanni Gábris, Angela Schippers, Norbert Wagner, Gergely Berta, Kornélia Farkas, Péter Balogh

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Quantitative Analysis of NKX2-3 Expression in Human Colon: An Immunohistochemical Study.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2024
    Article
  3. ILC3: a case of conflicted identity.Frontiers in immunology · 2023
    Review
  4. Article
  5. 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

8 authors at 2 institutions in 2 countries.

Dóra VojkovicsDepartment of Immunology and Biotechnology, Clinical Center, University of Pécs, Pécs, Hungary.
Zoltán KellermayerDepartment of Immunology and Biotechnology, Clinical Center, University of Pécs, Pécs, Hungary.
Fanni GábrisDepartment of Immunology and Biotechnology, Clinical Center, University of Pécs, Pécs, Hungary.
Angela SchippersDepartment of Pediatrics, University Hospital RWTH, Aachen, Germany.
Norbert WagnerDepartment of Pediatrics, University Hospital RWTH, Aachen, Germany.
Gergely BertaCentral Electron Microscope Laboratory, Department of Medical Biology, Medical School, University of Pécs, Pécs, Hungary.
Kornélia FarkasDepartment of Bioanalytics, Medical School, University of Pécs, Pécs, Hungary.
Péter BaloghDepartment of Immunology and Biotechnology, Clinical Center, University of Pécs, Pécs, Hungary.
University of Pecs · HURWTH Aachen University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Seeding of leukocytes to developing lymphoid tissues in embryonic and early postnatal age and to the mucosa throughout adulthood depends on the interaction between endothelial MAdCAM-1 addressin and its cognate ligand α4β7 integrin. Nkx2-3 as a transcriptional regulator of MAdCAM-1 controls vascular patterning in visceral lymphoid tissues in mice, and has been identified as a susceptibility factor for inflammatory bowel diseases in humans, associated with lymphoid neogenesis in the inflamed intestines. The role of Nkx2-3 in the organogenesis of the solitary intestinal lymphoid tissues (SILTs) involving type 3 innate lymphoid cells (ILC3) is still unknown. Here we investigated the effect of Nkx2-3 on the postnatal distribution of intestinal ILC3s and the development of SILTs, comparing these to mice lacking MAdCAM-1, but preserving Nkx2-3. At 1 week of age small intestines (SI) contained significantly higher number of ILC3s relative to the colon, with a substantial reduction in MAdCAM-1

Indexed as

Immunity, InnateAnimalsBiomarkersCell Adhesion MoleculesHomeodomain ProteinsImmunophenotypingIntestinal MucosaLymph NodesLymphocytesMiceMice, KnockoutMucoproteinsPeyer's PatchesRNA, MessengerTranscription FactorsBiomarkersCell Adhesion MoleculesHomeodomain ProteinsMadcam1 protein, mouseMucoproteinsNkx2.3 protein, mouseRNA, MessengerTranscription FactorscryptopatchILC3isolated lymphoid follicleMAdCAM-1NKX2-3

Identifiers

PMID30891037
PMCPMC6413488
OpenAlexW2919894495

What OpenQuestion holds

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LicenceCC BY
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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.