Evidence map›Paper›PMID 20059481›Full record

ArticleClinical and experimental immunology2010

Islet inflammation and CXCL10 in recent-onset type 1 diabetes.

B O Roep, F S Kleijwegt, A G S van Halteren, V Bonato, U Boggi, F Vendrame, P Marchetti, F Dotta

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03369821 (Understanding Beta-cell Destruction Through the Study of EXtremely Early-onset Type 1 Diabetes), which is not on this map. Cited by 111 papers.

0numbers the graph read from it
0cells of the map it votes in
111citing papers in PubMed
9.3field-weighted citation impact, top 2% 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.

NCT03369821 recruitingnot on this mapstarted 2017, after this paper: background citation

Understanding Beta-cell Destruction Through the Study of EXtremely Early-onset Type 1 Diabetes (A Musketeers' Memorandum Study)

TypeobservationalSponsorUniversity of ExeterRan2017 to 2028Enrolled300ConditionsType1 Diabetes MellitusArmsBeta Cell Loss and Immune Function, Immune Function with RNAseq
3 · Its place in the literature

Who cites it

111 citing papers in PubMed, 181 citations in OpenAlex.

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  9. From bats to humans: uncoveringbioRxiv : the preprint server for biology · 2026
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51 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

8 authors at 5 institutions in 2 countries.

B O RoepDepartment of Immunohaematology and Blood Transfusion, Leiden University Medical Center, Leiden, the Netherlands.
F S Kleijwegt
A G S van Halteren
V Bonato
U Boggi
F Vendrame
P Marchetti
F Dotta
Leiden University Medical Center · NLUniversity of Siena · ITFondazione Umberto Di Mario · ITOspedale Cisanello · ITUniversity of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 1 diabetes results from a T cell-mediated destruction of insulin-producing pancreatic beta cells. Little is known on local factors contributing to migration of T cells to pancreatic tissue. We recently demonstrated evidence of viral infection in beta cells in several recent-onset type 1 diabetes patients. Islet inflammation was analysed in a series of new- or recent-onset type 1 diabetic patients and non-diabetic control subjects. Autoimmune T cell reactivity was studied in lymphocytes derived from pancreas-draining lymph nodes of one recent-onset type 1 diabetes patient in partial clinical remission. Insulitic lesions were characterized by presence of beta cells, elevated levels of the chemokine CXCL10 and infiltration of lymphocytes expressing the corresponding chemokine receptor CXCR3 in all pancreatic lesions of type 1 diabetes patients, regardless of enterovirus infection of beta cells. CXCR3 and CXCL10 were undetectable in pancreata of non-diabetic control subjects. T cells isolated from draining lymph nodes of a recent-onset patient with virally infected beta cells and in clinical remission reacted with multiple islet autoantigens and displayed a mixed interferon (IFN)-gamma/interleukin (IL)-10 cytokine pattern. Our data point to CXCL10 as an important cytokine in distressed islets that may contribute to inflammation leading to insulitis and beta cell destruction, regardless of local viral infection. We demonstrate further pro- and anti-inflammatory islet autoreactivity, indicating that different adaptive and innate immune responses may contribute to insulitis and beta cell destruction.

Indexed as

AdolescentAdultChemokine CXCL10Child, PreschoolDiabetes Mellitus, Type 1EnterovirusEnterovirus InfectionsFemaleGene Expression RegulationHumansImmunity, CellularInflammationInsulin-Secreting CellsInterferon-gammaInterleukin-10Lymph NodesChemokine CXCL10CXCL10 protein, humanCXCR3 protein, humanIL10 protein, humanInterferon-gammaInterleukin-10Receptors, CXCR3

Identifiers

PMID20059481
PMCPMC2819499
OpenAlexW2103302952

What OpenQuestion holds

Textmetadata
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.