Evidence map›Paper›PMID 34113344›Full record

ArticleFrontiers in immunology2021

Characterization of Human CD4 T Cells Specific for a C-Peptide/C-Peptide Hybrid Insulin Peptide.

Timothy A Wiles, Anita Hohenstein, Laurie G Landry, Mylinh Dang, Roger Powell, Perrin Guyer, Eddie A James, Maki Nakayama, Kathryn Haskins, Thomas Delong and 1 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. The immunology of type 1 diabetes.Nature reviews. Immunology · 2024
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Activation pathways that drive CD4Immunological reviews · 2022
    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

11 authors.

Timothy A WilesDepartment of Pharmaceutical Sciences, University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences, Aurora, CO, United States.
Anita HohensteinDepartment of Pharmaceutical Sciences, University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences, Aurora, CO, United States.
Laurie G LandryBarbara Davis Center for Childhood Diabetes, University of Colorado School of Medicine, Aurora, CO, United States.
Mylinh DangDepartment of Pharmaceutical Sciences, University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences, Aurora, CO, United States.
Roger PowellDepartment of Pharmaceutical Sciences, University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences, Aurora, CO, United States.
Perrin GuyerDepartment of Translational Research, Benaroya Research Institute at Virginia Mason, Seattle, WA, United States.
Eddie A JamesDepartment of Translational Research, Benaroya Research Institute at Virginia Mason, Seattle, WA, United States.
Maki NakayamaDepartment of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO, United States.
Kathryn HaskinsDepartment of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO, United States.
Thomas DelongDepartment of Pharmaceutical Sciences, University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences, Aurora, CO, United States.
Rocky L BakerDepartment of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO, United States.

Funding

University of Colorado Anschutz Medical Campus DRCP30DK116073 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI LORI SUSSEL · 2020 to 2026
$10.8M
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
Multiple Autoantigens/Multiple Epitopes of Type 1DMR01DK032083 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI MICHELS, AARON W · 1986 to 2025
$6.9M
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
Characterize the Landscape and Origin of Hybrid Peptides in Beta CellsR01DK119529 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI THOMAS DELONG · 2018 to 2026
$4.8M
Insulin Specific T Cell Response Shaped by Diabetes Protective MHC Class II MoleculesR01DK108868 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI AARON W MICHELS · 2017 to 2026
$3.6M
T cell repertoire for hybrid insulin peptidesR01DK122566 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI HASKINS, KATHRYN M · 2019 to 2022
$2.0M
Responses to Hybrid Insulin Peptides as Biomarkers of Disease Activity in Human Type 1 DiabetesR01AI146202 · NIAID · UNIVERSITY OF COLORADO DENVER · PI BAKER, ROCKY LEE · 2020 to 2024
$1.9M
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
NIAID NIH HHS R01 AI146202NIAID NIH HHS R21 AI133059NIDDK NIH HHS P30 DK116073NIDDK NIH HHS R01 DK032083NIDDK NIH HHS R01 DK081166NIDDK NIH HHS R01 DK099317NIDDK NIH HHS R01 DK108868NIDDK NIH HHS R01 DK119529NIDDK NIH HHS R01 DK122566
6 · The paper itself

Abstract

Hybrid Insulin Peptides (HIPs), which consist of insulin fragments fused to other peptides from β-cell secretory granule proteins, are CD4 T cell autoantigens in type 1 diabetes (T1D). We have studied HIPs and HIP-reactive CD4 T cells extensively in the context of the non-obese diabetic (NOD) mouse model of autoimmune diabetes and have shown that CD4 T cells specific for HIPs are major contributors to disease pathogenesis. Additionally, in the human context, HIP-reactive CD4 T cells can be found in the islets and peripheral blood of T1D patients. Here, we performed an in-depth characterization of the CD4 T cell response to a C-peptide/C-peptide HIP (HIP11) in human T1D. We identified the TCR expressed by the previously-reported HIP11-reactive CD4 T cell clone E2, which was isolated from the peripheral blood of a T1D patient, and determined that it recognizes HIP11 in the context of HLA-DQ2. We also identified a HIP11-specific TCR directly in the islets of a T1D donor and demonstrated that this TCR recognizes a different minimal epitope of HIP11 presented by HLA-DQ8. We generated and tested an HLA-DQ2 tetramer loaded with HIP11 that will enable direct

Indexed as

AutoantigensCD4-Positive T-LymphocytesC-PeptideDiabetes Mellitus, Type 1EpitopesFemaleHLA-DQ AntigensHumansInsulinIslets of LangerhansK562 CellsMaleReceptors, Antigen, T-CellAutoantigensC-PeptideEpitopesHLA-DQ2 antigenHLA-DQ AntigensInsulinReceptors, Antigen, T-CellautoimmunityCD4hybrid insulin peptidesmass spectrometryneoepitopetetramertype 1 diabetes

Identifiers

PMID34113344
PMCPMC8185328

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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.