Evidence map›Paper›PMID 31132145›Full record

ReviewClinical and experimental immunology2019

HIPs and HIP-reactive T cells.

T A Wiles, T Delong

Open access · bronzeAbstract readReview
In one paragraph

Review in Clinical and experimental immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 19 citations in OpenAlex.

  1. Crinophagy in Pancreatic Beta Cells: From Insulin Granule Turnover to Diabetes Pathogenesis.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Spliced HLA-bound peptides: a Black Swan event in immunology.Clinical and experimental immunology · 2021
    Review
  10. Article
  11. Review
  12. Review
  13. Are There Indeed Spliced Peptides in the Immunopeptidome?Molecular & cellular proteomics : MCP · 2021
    Article
  14. Article
  15. Historical and new insights into pathogenesis of type 1 diabetes.Clinical and experimental immunology · 2019
    Article
  16. Hybrid insulin peptides are neo-epitopes for CD4 T cells in autoimmune diabetes.Current opinion in endocrinology, diabetes, and obesity · 2019
    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.

T A WilesSkaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz, Aurora, CO, USA.ORCID 0000-0002-9059-0061
T DelongSkaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz, Aurora, CO, USA.ORCID 0000-0002-3199-9385
University of Montana · US

Funding

Characterize the Landscape and Origin of Hybrid Peptides in Beta CellsR01DK119529 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI THOMAS DELONG · 2018 to 2026
$4.8M
NIDDK NIH HHS R01 DK119529
6 · The paper itself

Abstract

Mounting evidence implicates hybrid insulin peptides (HIPs) as important autoantigens in the development of type 1 diabetes (T1D). These fusion peptides formed between insulin and other pancreatic beta cell-derived peptides contain non-genomically encoded amino acid sequences, making them plausible targets for autoreactive T cells in T1D. HIPs are detectable by mass spectrometry in human and murine islets and are targeted by diabetes-inducing T cells in non-obese diabetic mice as well as by T cells isolated from the residual pancreatic islets of human organ donors with T1D. The discovery of HIPs comes with numerous new challenges, as well as opportunities to study the pathogenesis of T1D. Here we review the original discovery of HIPs and describe recent studies investigating the role of HIP-reactive T cells in the development of diabetes. We also discuss potential mechanisms that may be responsible for the generation of HIPs in beta cells and describe challenges that need to be addressed in the field of mass spectrometry to enable the discovery of new HIPs. The identification of these potentially disease-driving antigens in T1D is of key interest to the field as it may provide new tools to predict, prevent and potentially reverse the disease.

Indexed as

Amino Acid SequenceAnimalsAutoantigensAutoimmunityCD4-Positive T-LymphocytesDiabetes Mellitus, Type 1HumansInsulinInsulin-Secreting CellsMice, Inbred NODPeptidesAutoantigensInsulinPeptidesantigensautoimmunitydiabetesepitopespeptides

Identifiers

PMID31132145
PMCPMC6857078
OpenAlexW2948012768

What OpenQuestion holds

Textmetadata
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.