Evidence map›Paper›PMID 26458384›Full record

ReviewCurrent diabetes reports2015

Molecular Interactions Governing Autoantigen Presentation in Type 1 Diabetes.

Maki Nakayama, Kimberly M Simmons, Aaron W Michels

Open access · greenAbstract readReview
In one paragraph

Review in Current diabetes reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Self-Antigens Targeted by Regulatory T Cells in Type 1 Diabetes.International journal of molecular sciences · 2022
    Review
  3. Review
  4. Article
  5. Article
  6. Rationally designed small molecules to prevent type 1 diabetes.Current opinion in endocrinology, diabetes, and obesity · 2019
    Review
  7. Prediction and prevention of type 1 diabetes in children.Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology · 2019
    Article
  8. Review
  9. Autoreactive T cells in type 1 diabetes.The Journal of clinical investigation · 2017
    Review
  10. Article
  11. Review
  12. Review
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

3 authors at 1 institution in 1 country.

Maki NakayamaBarbara Davis Center for Childhood Diabetes, University of Colorado School of Medicine, Aurora, CO, USA.
Kimberly M SimmonsBarbara Davis Center for Childhood Diabetes, University of Colorado School of Medicine, Aurora, CO, USA.
Aaron W MichelsBarbara Davis Center for Childhood Diabetes, University of Colorado School of Medicine, Aurora, CO, USA. Aaron.Michels@ucdenver.edu.
University of Colorado Denver · US

Funding

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
Training Program in Diabetes ResearchT32DK063687 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Andrea Steck · 2002 to 2026
$5.2M
Small Molecules Targeting Allele Specific MHC Class II PresentationK08DK095995 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI MICHELS, AARON W · 2012 to 2016
$762k
NIDDK NIH HHS K08 DK095995NIDDK NIH HHS K08DK095995NIDDK NIH HHS R01 DK099317NIDDK NIH HHS R01DK099317NIDDK NIH HHS T32 DK063687
6 · The paper itself

Abstract

Type 1 diabetes is a chronic autoimmune disease resulting from T cell-mediated destruction of insulin-producing beta cells within pancreatic islets. Disease incidence has increased significantly in the last two decades, especially in young children. Type 1 diabetes is now predictable in humans with the measurement of serum islet autoantibodies directed against insulin and beta cell proteins. Knowledge regarding the presentation of insulin and islet antigens to T cells has increased dramatically over the last several years. Here, we review the trimolecular complex in diabetes, which consists of a major histocompatibility molecule,self-peptide, and T cell receptor, with a focus on insulin peptide presentation to T cells. With this increased understanding of how antigens are presented to T cells comes the hope for improved therapies for type 1 diabetes prevention.

Indexed as

AnimalsAutoantigensDiabetes Mellitus, Type 1HLA AntigensHumansInsulinReceptors, Antigen, T-CellT-LymphocytesAutoantigensHLA AntigensInsulinReceptors, Antigen, T-CellAutoimmunityDiabetesHLAInsulinT cells

Identifiers

PMID26458384
PMCPMC4807868
OpenAlexW2182568023

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.