Evidence map›Paper›PMID 36508037›Full record

ArticleDiabetologia2023

Gene expression profiling in NOD mice reveals that B cells are highly educated by the pancreatic environment during autoimmune diabetes.

Joanne Boldison, Jessica R Hopkinson, Joanne Davies, James A Pearson, Pia Leete, Sarah Richardson, Noel G Morgan, F Susan Wong

Open access · hybridAbstract read
In one paragraph

Article in Diabetologia, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 13% 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, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Expanding the Role of Continuous Glucose Monitoring in Modern Diabetes Care Beyond Type 1 Disease.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2023
    Review
  5. Review
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 1 country.

Joanne BoldisonDepartment of Clinical and Biomedical Sciences, University of Exeter, Exeter, UK. J.Boldison@Exeter.ac.uk.
Jessica R HopkinsonDepartment of Clinical and Biomedical Sciences, University of Exeter, Exeter, UK.
Joanne DaviesDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, UK.
James A PearsonDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, UK.
Pia LeeteDepartment of Clinical and Biomedical Sciences, University of Exeter, Exeter, UK.
Sarah RichardsonDepartment of Clinical and Biomedical Sciences, University of Exeter, Exeter, UK.
Noel G MorganDepartment of Clinical and Biomedical Sciences, University of Exeter, Exeter, UK.
F Susan WongDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, UK.
University of Exeter · GBCardiff University · GB

Funding

Diabetes UK 19/0006032Medical Research Council MR/K021141/1
6 · The paper itself

Abstract

aims/hypothesisB cells play an important role in driving the development of type 1 diabetes; however, it remains unclear how they contribute to local beta cell destruction during disease progression. Here, we use gene expression profiling of B cell subsets identified in inflamed pancreatic tissue to explore their primary functional role during the progression of autoimmune diabetes.

methodsTranscriptional profiling was performed on FACS-sorted B cell subsets isolated from pancreatic islets and the pancreatic lymph nodes of NOD mice.

resultsB cells are highly modified by the inflamed pancreatic tissue and can be distinguished by their transcriptional profile from those in the lymph nodes. We identified both a discrete and a core shared gene expression profile in islet CD19 CONCLUSIONS/

interpretationOur study provides a detailed transcriptional analysis of islet B cells. Specific gene signatures and interaction networks have been identified that point towards a functional role for B cells in driving autoimmune diabetes.

Indexed as

Diabetes Mellitus, Type 1Islets of LangerhansAnimalsGene Expression ProfilingMiceMice, Inbred NODPancreasAutoimmunityB cellsPancreatic isletsTLR7Type 1 diabetes

Identifiers

PMID36508037
PMCPMC9892163
OpenAlexW4311204355

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.