Evidence map›Paper›PMID 16123363›Full record

ArticleDiabetes2005

LEW.1WR1 rats develop autoimmune diabetes spontaneously and in response to environmental perturbation.

John P Mordes, Dennis L Guberski, Jean H Leif, Bruce A Woda, Joan F Flanagan, Dale L Greiner, Edward H Kislauskis, Rebecca S Tirabassi

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

25 citing papers in PubMed, 55 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

John P MordesBioMedical Research Models, 67 Millbrook St., Suite 422, Worcester, MA 01606, USA.
Dennis L Guberski
Jean H Leif
Bruce A Woda
Joan F Flanagan
Dale L Greiner
Edward H Kislauskis
Rebecca S Tirabassi
Biomedical Research Models (United States) · USUniversity of Massachusetts Chan Medical School · US

Funding

PILOT AND FEASIBILITY PROGRAMP30DK032520 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI CZECH, MICHAEL P · 1986 to 2010
$14.6M
EXPERIMENTAL JUVENILE TYPE DIABETESR01DK025306 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI GREINER, DALE LESLIE · 1994 to 2008
$3.8M
GENETICS OF AUTOIMMUNITY IN BB RATSR01DK049106 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI GREINER, DALE LESLIE · 1995 to 2006
$2.3M
New Rat Model of Autoimmune Diabetes And ArthritisR43DK060374 · NIDDK · BIOMEDICAL RESEARCH MODELS, INC. · PI GUBERSKI, DENNIS L. · 2001 to 2002
$343k
New Model For Virus Induced AutoimmunityR41RR019260 · NCRR · BIOMEDICAL RESEARCH MODELS, INC. · PI GUBERSKI, DENNIS L. · 2004 to 2004
$320k
EXPERIMENTAL JUVENILE-TYPE DIABETESR37DK025306 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI ROSSINI, ALDO A · 1986 to 1993
–
NCRR NIH HHS 1R41RR019260NCRR NIH HHS R41 RR019260NCRR NIH HHS R41 RR019260-01A1NIDDK NIH HHS DK25306NIDDK NIH HHS DK32520NIDDK NIH HHS DK49106NIDDK NIH HHS P30 DK032520NIDDK NIH HHS R01 DK025306NIDDK NIH HHS R01 DK049106NIDDK NIH HHS R43 DK060374-01PHS HHS 1R43K60374
6 · The paper itself

Abstract

We describe a new rat model of autoimmune diabetes that arose in a major histocompatibility complex congenic LEW rat. Spontaneous diabetes in LEW.1WR1 rats (RT1(u/u/a)) occurs with a cumulative frequency of approximately 2% at a median age of 59 days. The disease is characterized by hyperglycemia, glycosuria, ketonuria, and polyuria. Both sexes are affected, and islets of acutely diabetic rats are devoid of beta-cells, whereas alpha- and delta-cell populations are spared. The peripheral lymphoid phenotype is normal, including the fraction of ART2(+) regulatory T-cells. We tested the hypothesis that the expression of diabetes would be increased by immunological perturbation of innate or adaptive immunity. Treatment of young rats with depleting anti-ART2.1 monoclonal antibody increased the frequency of diabetes to 50%. Treatment with the toll-like receptor 3 ligand polyinosinic:polycytidylic acid increased the frequency of diabetes to 100%. All diabetic rats exhibited end-stage islets. The LEW.1WR1 rat is also susceptible to collagen-induced arthritis but is free of spontaneous thyroiditis. The LEW.1WR1 rat provides a new model for studying autoimmune diabetes and arthritis in an animal with a genetic predisposition to both disorders that can be amplified by environmental perturbation.

Indexed as

AnimalsAntibodies, MonoclonalArthritisCollagenDiabetes MellitusDisease Models, AnimalFemaleLipopolysaccharidesMalePoly I-CRatsTime FactorsAntibodies, MonoclonalCollagenLipopolysaccharidesPoly I-C

Identifiers

PMID16123363
PMCPMC1283095
OpenAlexW2149914595

What OpenQuestion holds

Textmetadata
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.