Evidence map›Paper›PMID 28420714›Full record

ReviewJournal of molecular endocrinology2017

Pancreatic islet inflammation: an emerging role for chemokines.

J Jason Collier, Tim E Sparer, Michael D Karlstad, Susan J Burke

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of molecular endocrinology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
4.0field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 63 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. The immunology of sickness metabolism.Cellular & molecular immunology · 2024
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  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

4 authors at 4 institutions in 2 countries.

J Jason CollierLaboratory of Islet Biology and InflammationPennington Biomedical Research Center, Baton Rouge, Louisiana, USA Jason.collier@pbrc.edu.
Tim E SparerDepartment of MicrobiologyUniversity of Tennessee, Knoxville, Knoxville, Tennessee, USA.
Michael D KarlstadDepartment of SurgeryGraduate School of Medicine, University of Tennessee Health Science Center, Knoxville, Tennessee, USA.
Susan J BurkeLaboratory of ImmunogeneticsPennington Biomedical Research Center, Baton Rouge, Louisiana, USA.
Immungenetics (Germany) · DEKnoxville College · USUniversity of Tennessee at Knoxville · USUniversity of Tennessee Health Science Center · US

Funding

THE ROLE OF PROTEIN MALNUTRITION ON CIRCADIAN PHYSIOLOGY OF C57BL/6J MOUSE DAMSP20RR021945 · NCRR · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2006 to 2011
$9.5M
Mentoring Obesity and Diabetes Research in LouisianaP20GM103528 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2012 to 2015
$8.8M
Transgenics CoreP30GM118430 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI GETTYS, THOMAS W · 2016 to 2020
$5.8M
Development of an Atmospheric Plasma Applicator to Treat Chronic WoundsR44GM099207 · NIGMS · ADVANCED PLASMA PRODUCTS, INC. · PI JAMES, GARTH A, KARLSTAD, MICHAEL D · 2013 to 2014
$2.2M
Viral Chemokine Alteration of Neutrophil FunctionsR01AI071042 · NIAID · UNIVERSITY OF TENNESSEE KNOXVILLE · PI SPARER, TIMOTHY E · 2008 to 2012
$1.6M
Development of an Atmospheric Plasma Applicator to Treat Chronic WoundsR43GM099207 · NIGMS · ADVANCED PLASMA PRODUCTS, INC. · PI KELLY-WINTENBERG, KIMBERLY D · 2011 to 2011
$419k
NCRR NIH HHS P20 RR021945NIAID NIH HHS R01 AI071042NIGMS NIH HHS P20 GM103528NIGMS NIH HHS P30 GM118430NIGMS NIH HHS R43 GM099207NIGMS NIH HHS R44 GM099207
6 · The paper itself

Abstract

Both type 1 and type 2 diabetes exhibit features of inflammation associated with alterations in pancreatic islet function and mass. These immunological disruptions, if unresolved, contribute to the overall pathogenesis of disease onset. This review presents the emerging role of pancreatic islet chemokine production as a critical factor regulating immune cell entry into pancreatic tissue as well as an important facilitator of changes in tissue resident leukocyte activity. Signaling through two specific chemokine receptors (i.e., CXCR2 and CXCR3) is presented to illustrate key points regarding ligand-mediated regulation of innate and adaptive immune cell responses. The prospective roles of chemokine ligands and their corresponding chemokine receptors to influence the onset and progression of autoimmune- and obesity-associated forms of diabetes are discussed.

Indexed as

Adaptive ImmunityAnimalsChemokinesDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2Disease Models, AnimalGene Expression RegulationHumansImmunity, InnateInflammationIslets of LangerhansLeukocytesObesityReceptors, CXCR3Receptors, Interleukin-8BSignal TransductionChemokinesCXCR3 protein, humanReceptors, CXCR3Receptors, Interleukin-8Bchemokinecytokinediabetesinflammationislet

Identifiers

PMID28420714
PMCPMC5505180
OpenAlexW2607504197

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.