Evidence map›Paper›PMID 31166225›Full record

ReviewCurrent opinion in endocrinology, diabetes, and obesity2019

Hybrid insulin peptides are neo-epitopes for CD4 T cells in autoimmune diabetes.

Rocky L Baker, Braxton L Jamison, Kathryn Haskins

Abstract readReview
In one paragraph

Review in Current opinion in endocrinology, diabetes, and obesity, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
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  5. Review
  6. New and emerging therapies in type 1 diabetes mellitus.The Journal of clinical investigation · 2026
    Review
  7. Article
  8. Article
  9. Breakdown and Repair of Peripheral Immune Tolerance in Type 1 Diabetes.Cold Spring Harbor perspectives in medicine · 2024
    Review
  10. Aire mediates tolerance to insulin through thymic trimming of high-affinity T cell clones.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. De novo identification of CD4Nature methods · 2024
    Article
  12. Epitope-based precision immunotherapy of Type 1 diabetes.Human vaccines & immunotherapeutics · 2023
    Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. T-cell responses to hybrid insulin peptides prior to type 1 diabetes development.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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 2 institutions in 1 country.

Rocky L Baker
Braxton L Jamison
Kathryn Haskins
University of Colorado Denver · USUniversity of Colorado Anschutz Medical Campus · US

Funding

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
T cells reactive to Hybrid Insulin Peptides (HIPs) as biomarkers in autoimmune diabetesR21AI133059 · NIAID · UNIVERSITY OF COLORADO DENVER · PI BAKER, ROCKY LEE · 2018 to 2019
$428k
Immunological Tolerance to Hybrid Insulin PeptidesF31DK113693 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI JAMISON, BRAXTON LOCHRIDGE · 2018 to 2020
$79k
NIAID NIH HHS R21 AI133059NIAID NIH HHS T32 AI007405NIDDK NIH HHS F31 DK113693NIDDK NIH HHS R01 DK081166
6 · The paper itself

Abstract

purpose of reviewThe current review covers recent advances in our knowledge of the newest autoantigen neo-epitopes in type 1 diabetes (T1D): hybrid insulin peptides or HIPs. These ligands for autoreactive T cells are formed by peptide fusion, a novel posttranslational modification process that we first reported in 2016. RECENT

findingsTwo major HIPs in the nonobese diabetic mouse model, ligands for diabetogenic CD4 T-cell clones, have been incorporated into tetramers and used to track HIP-reactive T cells during progression of disease. HIPs have also been used in strategies for induction of antigen-specific tolerance and show promise for delaying or reversing disease in the nonobese diabetic mouse. Importantly, CD4 T cells reactive to various HIPs have been detected in the islets and peripheral blood mononuclear cell of T1D patients and newly developed human T-cell clones are being employed to gather more data on the phenotype and function of HIP-reactive T cells in patients. SUMMARY: These new hybrid insulin peptide epitopes may provide the basis for establishing autoreactive T cells as biomarkers of disease and as potential tolerogens for treatment of T1D.

Indexed as

AnimalsCD4-Positive T-LymphocytesDiabetes Mellitus, Type 1Epitopes, T-LymphocyteHumansInsulinMicePeptidesEpitopes, T-LymphocyteInsulinPeptides

Identifiers

PMID31166225
PMCPMC6830731
OpenAlexW2950108665

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.