Evidence map›Paper›PMID 29637711›Full record

ReviewThe FEBS journal2018

A guide to chemokines and their receptors.

Catherine E Hughes, Robert J B Nibbs

Registry-linked trialOpen access · hybridAbstract readReview
In one paragraph

Review in The FEBS journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05025787 (EN20-01), which is not on this map. Cited by 831 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
831citing papers in PubMed, 4 pooled it
29.4field-weighted citation impact, top 1% 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.

NCT05025787 phase2completednot on this mapstarted 2021, after this paper: background citation

EN20-01: A 24 Week Study to Evaluate the Safety and Efficacy of CNTX-6970 in Subjects With Moderate to Severe Knee Osteoarthritis Pain.

TypeinterventionalSponsorMaurizio Fava, MDRan2021 to 2024Enrolled55ConditionsKnee OsteoarthritisArmsCNTX-6970, Placebo
3 · Its place in the literature

Who cites it

831 citing papers in PubMed, 4 syntheses or guidelines pooled it, 1,390 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Review
  7. Article
  8. A Versatile Anti-CXCR5 Monoclonal Antibody (CxCurrent issues in molecular biology · 2026
    Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. TMAO Correlates with Transcriptomic Signatures of Leukocyte Activation and Systemic Inflammation Following Burn Injury.Journal of burn care & research : official publication of the American Burn Association · 2026
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Potential of Saliva in Stroke Patients: A Review.International journal of molecular sciences · 2026
    Review
  20. Article

771 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Catherine E HughesInstitute of Infection, Inflammation & Immunity, College of Medical, Veterinary and Life Sciences, University of Glasgow, UK.
Robert J B NibbsInstitute of Infection, Inflammation & Immunity, College of Medical, Veterinary and Life Sciences, University of Glasgow, UK.ORCID 0000-0002-8150-0044
University of Glasgow · GB

Funding

Medical Research Council G0901113Medical Research Council M019764/1Medical Research Council MR/M019764/1Medical Research Council MR/N023625/1Medical Research Council N023625/1Wellcome TrustWellcome Trust 206284/Z/17/Z
6 · The paper itself

Abstract

The chemokines (or chemotactic cytokines) are a large family of small, secreted proteins that signal through cell surface G protein-coupled heptahelical chemokine receptors. They are best known for their ability to stimulate the migration of cells, most notably white blood cells (leukocytes). Consequently, chemokines play a central role in the development and homeostasis of the immune system, and are involved in all protective or destructive immune and inflammatory responses. Classically viewed as inducers of directed chemotactic migration, it is now clear that chemokines can stimulate a variety of other types of directed and undirected migratory behavior, such as haptotaxis, chemokinesis, and haptokinesis, in addition to inducing cell arrest or adhesion. However, chemokine receptors on leukocytes can do more than just direct migration, and these molecules can also be expressed on, and regulate the biology of, many nonleukocytic cell types. Chemokines are profoundly affected by post-translational modification, by interaction with the extracellular matrix (ECM), and by binding to heptahelical 'atypical' chemokine receptors that regulate chemokine localization and abundance. This guide gives a broad overview of the chemokine and chemokine receptor families; summarizes the complex physical interactions that occur in the chemokine network; and, using specific examples, discusses general principles of chemokine function, focusing particularly on their ability to direct leukocyte migration.

Indexed as

AnimalsCell MovementChemokinesChemotaxisGlycosaminoglycansHomeostasisHost-Pathogen InteractionsHumansInfectionsInflammationProtein MultimerizationProtein Processing, Post-TranslationalReceptors, ChemokineChemokinesGlycosaminoglycansReceptors, Chemokineatypical chemokine receptorcell migrationchemokinechemokine receptorglycosaminoglycanimmune surveillanceinflammationleukocyteoligomerizationprotease

Identifiers

PMID29637711
PMCPMC6120486
OpenAlexW2797069917

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.