Evidence map›Paper›PMID 20489610›Full record

ReviewCurrent opinion in endocrinology, diabetes, and obesity2010

The anti-insulin trimolecular complex in type 1 diabetes.

Aaron W Michels, Maki Nakayama

Abstract readReview
In one paragraph

Review in Current opinion in endocrinology, diabetes, and obesity, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Type 1 diabetes: A predictable disease.World journal of diabetes · 2015
    Review
  5. Monoclonal antibody blocking the recognition of an insulin peptide-MHC complex modulates type 1 diabetes.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  6. Targeting the trimolecular complex.Clinical immunology (Orlando, Fla.) · 2013
    Review
  7. Article
  8. Article
  9. Risk factors and primary prevention trials for type 1 diabetes.International journal of biological sciences · 2013
    Review
  10. Article
  11. Article
  12. Article
  13. 2011 Update: antigen-specific therapy in type 1 diabetes.Current opinion in endocrinology, diabetes, and obesity · 2011
    Review
  14. Immune intervention in type 1 diabetes.Seminars in immunology · 2011
    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

2 authors at 1 institution in 1 country.

Aaron W MichelsBarbara Davis Center for Childhood Diabetes, University of Colorado Denver, Aurora, Colorado 80045, USA. Aaron.Michels@ucdenver.edu
Maki Nakayama
University of Colorado Denver · US

Funding

Small Molecules Targeting Allele Specific MHC Class II PresentationK08DK095995 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI MICHELS, AARON W · 2012 to 2016
$762k
STRUCTURE PEPTIDE/CONSERVED T CELL RECEPTOR DETERMINING DIABETESR00DK080885 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI NAKAYAMA, MAKI · 2010 to 2012
$742k
NIDDK NIH HHS K08 DK095995NIDDK NIH HHS R00 DK080885
6 · The paper itself

Abstract

purpose of reviewDescription of the immunologic components needed for autoimmune diabetes. RECENT

findingsThe major histocompatability complex (MHC) class II molecules are the primary susceptibility genes for many autoimmune diseases, including type 1 diabetes. Understanding of the structural interaction between MHC molecules, antigenic peptides, and T-cell receptors (the three components of the trimolecular complex) has increased greatly over the past several years. The components of the anti-insulin trimolecular complex and findings that insulin is a key autoantigen in type 1 diabetes are reviewed. SUMMARY: The anti-insulin trimolecular complex is well defined in the nonobese diabetic mouse model. Insulin and specifically, the amino acid sequence 9 to 23 of the insulin B chain, represents a primary antigenic target for islet autoimmunity in the nonobese diabetic mouse model of type 1 diabetes with a specific mutation of this peptide preventing all diabetes. Initial studies suggest the human homologs of the anti-insulin trimolecular complex may be relevant in human disease.

Indexed as

AnimalsAutoantibodiesDiabetes Mellitus, Type 1HumansInsulinMacromolecular SubstancesMajor Histocompatibility ComplexMiceModels, BiologicalReceptors, Antigen, T-CellAutoantibodiesInsulinMacromolecular SubstancesReceptors, Antigen, T-Cell

Identifiers

PMID20489610
PMCPMC4012426
OpenAlexW2018155985

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.