Evidence map›Paper›PMID 29881878›Full record

ArticleDiabetologia2018

Loss of CXCR3 expression on memory B cells in individuals with long-standing type 1 diabetes.

Wendy E Powell, Stephanie J Hanna, Claire N Hocter, Emma Robinson, Joanne Davies, Gareth J Dunseath, Stephen Luzio, Daniel Farewell, Li Wen, Colin M Dayan and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Diabetologia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Chemokines in Type 1 Diabetes Mellitus.Frontiers in immunology · 2021
    Article
  9. Review
  10. Review
  11. Article
  12. 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

13 authors at 3 institutions in 2 countries.

Wendy E PowellDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, CF14 4XN, UK.
Stephanie J HannaDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, CF14 4XN, UK.
Claire N HocterDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, CF14 4XN, UK.
Emma RobinsonDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, CF14 4XN, UK.
Joanne DaviesDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, CF14 4XN, UK.
Gareth J DunseathDiabetes Research Unit Cymru, Swansea University, Swansea, UK.
Stephen LuzioDiabetes Research Unit Cymru, Swansea University, Swansea, UK.
Daniel FarewellDivision of Population Medicine, Cardiff University School of Medicine, Cardiff, UK.
Li WenSection of Endocrinology, Yale University School of Medicine, New Haven, CT, USA.
Colin M DayanDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, CF14 4XN, UK.
David A PriceDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, CF14 4XN, UK.
Kristin LadellDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, CF14 4XN, UK.
F Susan WongDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, CF14 4XN, UK. wongfs@cardiff.ac.uk.ORCID 0000-0002-2812-8845
Cardiff University · GBSwansea University · GBYale University · US

Funding

Yale Diabetes Research CenterP30DK045735 · NIDDK · YALE UNIVERSITY · PI Kevan C Herold, GERALD I SHULMAN · 1993 to 2026
$44.0M
Diabetes UK 11/0004319NIDDK NIH HHS P30 DK045735Wellcome Trust 100326/Z/12/Z
6 · The paper itself

Abstract

aims/hypothesisIslet-specific autoantibodies can predict the development of type 1 diabetes. However, it remains unclear if B cells, per se, contribute to the causal pancreatic immunopathology. We aimed to identify phenotypic signatures of disease progression among naive and memory B cell subsets in the peripheral blood of individuals with type 1 diabetes.

methodsA total of 69 participants were recruited across two separate cohorts, one for discovery purposes and the other for validation purposes. Each cohort comprised two groups of individuals with type 1 diabetes (one with newly diagnosed type 1 diabetes and the other with long-standing type 1 diabetes) and one group of age- and sex-matched healthy donors. The phenotypic characteristics of circulating naive and memory B cells were investigated using polychromatic flow cytometry, and serum concentrations of various chemokines and cytokines were measured using immunoassays.

resultsA disease-linked phenotype was detected in individuals with long-standing type 1 diabetes, characterised by reduced C-X-C motif chemokine receptor 3 (CXCR3) expression on switched (CD27 CONCLUSIONS/

interpretationOur data reveal a statistically robust set of abnormalities that indicate an association between type 1 diabetes and long-term dysregulation of a chemokine ligand/receptor system that controls B cell migration.

Indexed as

AdultB-LymphocytesChemokine CXCL11ChemokinesDiabetes Mellitus, Type 1fas ReceptorFemaleHumansLeukocyte Common AntigensMaleReceptors, CXCR3T-LymphocytesTumor Necrosis Factor Receptor Superfamily, Member 7Young AdultChemokine CXCL11ChemokinesCXCL11 protein, humanCXCR3 protein, humanfas ReceptorLeukocyte Common AntigensReceptors, CXCR3Tumor Necrosis Factor Receptor Superfamily, Member 7AutoimmunityB220BAFFB cellsCD24CD95CXCL10CXCL11CXCR3Type 1 diabetes

Identifiers

PMID29881878
PMCPMC6061155
OpenAlexW2805560670

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.