Evidence map›Paper›PMID 33123134›Full record

ArticleFrontiers in immunology2020

CXCL14 Preferentially Synergizes With Homeostatic Chemokine Receptor Systems.

Ariadni Kouzeli, Paul J Collins, Mieke Metzemaekers, Max Meyrath, Martyna Szpakowska, Marc Artinger, Sofie Struyf, Paul Proost, Andy Chevigne, Daniel F Legler and 2 more

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 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.6field-weighted citation impact, top 14% 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

25 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

12 authors at 6 institutions in 4 countries.

Ariadni KouzeliDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Paul J CollinsInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.
Mieke MetzemaekersLaboratory of Molecular Immunology, Rega Institute for Medical Research, KU Leuven, Leuven, Belgium.
Max MeyrathDepartment of Infection and Immunity, Immuno-Pharmacology and Interactomics, Luxembourg Institute of Health (LIH), Esch-sur-Alzette, Luxembourg.
Martyna SzpakowskaDepartment of Infection and Immunity, Immuno-Pharmacology and Interactomics, Luxembourg Institute of Health (LIH), Esch-sur-Alzette, Luxembourg.
Marc ArtingerBiotechnology Institute Thurgau (BITg), University of Konstanz, Kreuzlingen, Switzerland.
Sofie StruyfLaboratory of Molecular Immunology, Rega Institute for Medical Research, KU Leuven, Leuven, Belgium.
Paul ProostLaboratory of Molecular Immunology, Rega Institute for Medical Research, KU Leuven, Leuven, Belgium.
Andy ChevigneDepartment of Infection and Immunity, Immuno-Pharmacology and Interactomics, Luxembourg Institute of Health (LIH), Esch-sur-Alzette, Luxembourg.
Daniel F LeglerBiotechnology Institute Thurgau (BITg), University of Konstanz, Kreuzlingen, Switzerland.
Matthias EberlDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Bernhard MoserDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
Cardiff University · GBLuxembourg Institute of Health · LUBiotechnology Institute Thurgau · CHRega Institute for Medical Research · BEKU Leuven · BEUniversity of Birmingham · GB

Funding

Medical Research Council MR/L018284/1
6 · The paper itself

Abstract

Reflecting their importance in immunity, the activity of chemokines is regulated on several levels, including tissue and context-specific expression and availability of their cognate receptor on target cells. Chemokine synergism, affecting both chemokine and chemokine receptor function, has emerged as an additional control mechanism. We previously demonstrated that CXCL14 is a positive allosteric modulator of CXCR4 in its ability to synergize with CXCL12 in diverse cellular responses. Here, we have extended our study to additional homeostatic, as well as a selection of inflammatory chemokine systems. We report that CXCL14 strongly synergizes with low (sub-active) concentrations of CXCL13 and CCL19/CCL21 in

Indexed as

beta-Arrestin 2Blood DonorsCalciumChemokine CCL19Chemokine CCL21Chemokine CXCL13Chemokines, CXCChemotaxisHEK293 CellsHomeostasisHumansProtein BindingReceptors, CCR7Receptors, CXCR4Receptors, CXCR5Signal TransductionARRB2 protein, humanbeta-Arrestin 2CalciumCCL19 protein, humanCCL21 protein, humanCCR7 protein, humanChemokine CCL19Chemokine CCL21Chemokine CXCL13Chemokines, CXCCXCL13 protein, humanCXCL14 protein, humanCXCR4 protein, humanCXCR5 protein, humanReceptors, CCR7Receptors, CXCR4Receptors, CXCR5CCR7cell localizationchemokinesCXCR4CXCR5migrationsignal transductionsynergism

Identifiers

PMID33123134
PMCPMC7570948
OpenAlexW3092561477

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.