Evidence map›Paper›PMID 24043895›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Cutting edge: CD4 T cells reactive to an islet amyloid polypeptide peptide accumulate in the pancreas and contribute to disease pathogenesis in nonobese diabetic mice.

Rocky L Baker, Thomas Delong, Gene Barbour, Brenda Bradley, Maki Nakayama, Kathryn Haskins

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 16% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. CD4Immunity · 2024
    Article
  7. Review
  8. Review
  9. Article
  10. Activation pathways that drive CD4Immunological reviews · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
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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

6 authors at 2 institutions in 1 country.

Rocky L BakerIntegrated Department of Immunology, University of Colorado at Denver School of Medicine and National Jewish Health, Denver, CO 80206.
Thomas Delong
Gene Barbour
Brenda Bradley
Maki Nakayama
Kathryn Haskins
National Jewish Health · USUniversity of Colorado Denver · US

Funding

Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
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 Dissection of Insulin Targeting in Anti-Islet AutoimmunityR01DK099317 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI AARON W MICHELS, Maki Nakayama · 2013 to 2026
$5.3M
Molecular Mechanisms of Immune ToleranceT32AI074491 · NIAID · NATIONAL JEWISH HEALTH · PI CAMBIER, JOHN C, PELANDA, ROBERTA · 2009 to 2023
$4.1M
STRUCTURE PEPTIDE/CONSERVED T CELL RECEPTOR DETERMINING DIABETESR00DK080885 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI NAKAYAMA, MAKI · 2010 to 2012
$742k
Post-Translational Modification of a Type 1 Diabetes AutoantigenK01DK094941 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI DELONG, THOMAS · 2012 to 2014
$367k
NCATS NIH HHS UL1 TR001082NIAID NIH HHS 5T32AI007405-20NIAID NIH HHS T32 AI007405NIDDK NIH HHS K01 DK094941NIDDK NIH HHS R00 DK080885NIDDK NIH HHS R01 DK081166NIDDK NIH HHS R01 DK099317
6 · The paper itself

Abstract

We previously reported a peptide KS20 from islet amyloid polypeptide (IAPP) to be the target Ag for a highly diabetogenic CD4 T cell clone BDC-5.2.9. To track IAPP-reactive T cells in NOD mice and determine how they contribute to the pathogenesis of type 1 diabetes, we designed a new I-Ag7 tetramer with high affinity for BDC-5.2.9 that contains the peptide KS20. We found that significant numbers of KS20 tetramer(+) CD4 T cells can be detected in the pancreas of prediabetic and diabetic NOD mice. To verify pathogenicity of IAPP-reactive cells, we sorted KS20 tetramer(+) cells and cloned them from uncloned T cell lines isolated from spleen and lymph nodes of diabetic mice. We isolated a new KS20-reactive Th1 CD4 T cell clone that rapidly transfers diabetes. Our results suggest that IAPP triggers a broad autoimmune response by CD4 T cells in NOD mice.

Indexed as

Adoptive TransferAnimalsAutoantigensAutoimmunityCD4-Positive T-LymphocytesCells, CulturedDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Histocompatibility Antigens Class IIIslet Amyloid PolypeptideLymph NodesMiceMice, Inbred C57BLMice, Inbred NODPancreasPrediabetic StateAutoantigensHistocompatibility Antigens Class III-A g7 antigenIslet Amyloid Polypeptide

Identifiers

PMID24043895
PMCPMC3815676
OpenAlexW2164971474

What OpenQuestion holds

Textmetadata
LicenceTDM
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.