Evidence map›Paper›PMID 21734016›Full record

ArticleDiabetes2011

Islet amyloid polypeptide is a target antigen for diabetogenic CD4+ T cells.

Thomas Delong, Rocky L Baker, Nichole Reisdorph, Richard Reisdorph, Roger L Powell, Michael Armstrong, Gene Barbour, Brenda Bradley, Kathryn Haskins

Open access · hybridAbstract read
In one paragraph

Article in Diabetes, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
5.0field-weighted citation impact, top 5% 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

43 citing papers in PubMed, 60 citations in OpenAlex.

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  20. Polyvaccine: joining the links in the cascade of type 1 diabetes.Clinical and experimental vaccine research · 2021
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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

9 authors at 2 institutions in 1 country.

Thomas DelongIntegrated Department of Immunology, University of Colorado Denver School of Medicine and National Jewish Health, Denver, Colorado, USA.
Rocky L Baker
Nichole Reisdorph
Richard Reisdorph
Roger L Powell
Michael Armstrong
Gene Barbour
Brenda Bradley
Kathryn Haskins
University of Colorado Denver · USNational Jewish Health · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR025780 · NCRR · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2008 to 2011
$61.3M
UCHSC DIABETES ENDOCRINOLOGY RESEARCH CENTERP30DK057516 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI HUTTON, JOHN C · 2000 to 2010
$14.0M
TRAINING PROGRAM IN IMMUNOLOGYT32AI007405 · NIAID · UNIVERSITY OF COLORADO DENVER · PI Laurel L Lenz, Raul Martin Torres · 1991 to 2026
$10.5M
Hybrid Peptides as Autoantigens for Diabetogenic CD4 T CellsR01DK081166 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI HASKINS, KATHRYN M, JAMES, EDDIE A · 2011 to 2024
$7.3M
Molecular Mechanisms of Immune ToleranceT32AI074491 · NIAID · NATIONAL JEWISH HEALTH · PI CAMBIER, JOHN C, PELANDA, ROBERTA · 2009 to 2023
$4.1M
Effector Function of Autoreactive Th1 T CellsR01DK050561 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI HASKINS, KATHRYN M · 1996 to 2010
$1.8M
ION TRAP for NJCS10RR023703 · NCRR · NATIONAL JEWISH HEALTH · PI REISDORPH, NICHOLE A · 2008 to 2008
$435k
NCRR NIH HHS S10 RR023703NCRR NIH HHS S10RR023703NCRR NIH HHS UL-1-RR-O25780NIAID NIH HHS T32 AI007405NIAID NIH HHS T32-AI-007405NIDDK NIH HHS P30 DK057516NIDDK NIH HHS P30-DK-057516NIDDK NIH HHS R01 DK050561NIDDK NIH HHS R01 DK081166NIDDK NIH HHS R01-DK-50561
6 · The paper itself

Abstract

objectiveTo investigate autoantigens in β-cells, we have used a panel of pathogenic T-cell clones that were derived from the NOD mouse. Our particular focus in this study was on the identification of the target antigen for the highly diabetogenic T-cell clone BDC-5.2.9. RESEARCH DESIGN AND

methodsTo purify β-cell antigens, we applied sequential size exclusion chromatography and reverse-phase high-performance liquid chromatography to membrane preparations of β-cell tumors. The presence of antigen was monitored by measuring the interferon-γ production of BDC-5.2.9 in response to chromatographic fractions in the presence of NOD antigen-presenting cells. Peak antigenic fractions were analyzed by ion-trap mass spectrometry, and candidate proteins were further investigated through peptide analysis and, where possible, testing of islet tissue from gene knockout mice.

resultsMass-spectrometric analysis revealed the presence of islet amyloid polypeptide (IAPP) in antigen-containing fractions. Confirmation of IAPP as the antigen target was demonstrated by the inability of islets from IAPP-deficient mice to stimulate BDC-5.2.9 in vitro and in vivo and by the existence of an IAPP-derived peptide that strongly stimulates BCD-5.2.9.

conclusionsIAPP is the target antigen for the diabetogenic CD4 T-cell clone BDC-5.2.9.

Indexed as

AnimalsAntigen-Presenting CellsAutoantigensCD4-Positive T-LymphocytesDiabetes Mellitus, Type 1Islet Amyloid PolypeptideIslets of LangerhansMass SpectrometryMiceMice, Inbred NODAutoantigensIslet Amyloid Polypeptide

Identifiers

PMID21734016
PMCPMC3161333
OpenAlexW2148119886

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.