Evidence map›Paper›PMID 24310561›Full record

ArticleDiabetologia2014

Islet infiltration, cytokine expression and beta cell death in the NOD mouse, BB rat, Komeda rat, LEW.1AR1-iddm rat and humans with type 1 diabetes.

Anne Jörns, Tanja Arndt, Andreas Meyer zu Vilsendorf, Jürgen Klempnauer, Dirk Wedekind, Hans-Jürgen Hedrich, Lorella Marselli, Piero Marchetti, Nagakatsu Harada, Yutaka Nakaya and 5 more

Open access · greenAbstract readComparative Study
PubMed Publisher
In one paragraph

Article in Diabetologia, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

49 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
  2. The influence of endocrine disruptors on the gut microbiota.Turkish journal of medical sciences · 2025
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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

15 authors at 5 institutions in 5 countries.

Anne JörnsInstitute of Clinical Biochemistry, Hannover Medical School, 30623, Hannover, Germany.
Tanja Arndt
Andreas Meyer zu Vilsendorf
Jürgen Klempnauer
Dirk Wedekind
Hans-Jürgen Hedrich
Lorella Marselli
Piero Marchetti
Nagakatsu Harada
Yutaka Nakaya
Gen-Sheng Wang
Fraser W Scott
Conny Gysemans
Chantal Mathieu
Sigurd Lenzen
Medizinische Hochschule Hannover · DEKU Leuven · BEOttawa Hospital Research InstituteTokushima University · JPUniversity of Pisa · IT

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

aims/hypothesisResearch on the pathogenesis of type 1 diabetes relies heavily on good animal models. The aim of this work was to study the translational value of animal models of type 1 diabetes to the human situation.

methodsWe compared the four major animal models of spontaneous type 1 diabetes, namely the NOD mouse, BioBreeding (BB) rat, Komeda rat and LEW.1AR1-iddm rat, by examining the immunohistochemistry and in situ RT-PCR of immune cell infiltrate and cytokine pattern in pancreatic islets, and by comparing findings with human data.

resultsAfter type 1 diabetes manifestation CD8(+) T cells, CD68(+) macrophages and CD4(+) T cells were observed as the main immune cell types with declining frequency, in infiltrated islets of all diabetic pancreases. IL-1β and TNF-α were the main proinflammatory cytokines in the immune cell infiltrate in NOD mice, BB rats and LEW.1AR1-iddm rats, as well as in humans. The Komeda rat was the exception, with IFN-γ and TNF-α being the main cytokines. In addition, IL-17 and IL-6 and the anti-inflammatory cytokines IL-4, IL-10 and IL-13 were found in some infiltrating immune cells. Apoptotic as well as proliferating beta cells were observed in infiltrated islets. In healthy pancreases no proinflammatory cytokine expression was observed. CONCLUSIONS/

interpretationWith the exception of the Komeda rat, the animal models mirror very well the situation in humans with type 1 diabetes. Thus animal models of type 1 diabetes can provide meaningful information on the disease processes in the pancreas of patients with type 1 diabetes.

Indexed as

ApoptosisDiabetes Mellitus, ExperimentalAnimalsB-LymphocytesCytokinesDiabetes Mellitus, Type 1Gene Expression RegulationHumansImmunohistochemistryInsulin-Secreting CellsInterferon-gammaMiceMice, Inbred NODRatsRats, Inbred BBRats, Inbred LewCytokinesInterferon-gammaTumor Necrosis Factor-alpha

Identifiers

PMID24310561
OpenAlexW1995684565

What OpenQuestion holds

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Registered trials

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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.