Evidence map›Paper›PMID 38778498›Full record

ArticleEuropean journal of immunology2024

Human insulin as both antigen and protector in type 1 diabetes.

Nitin P Amdare, Leonard D Shultz, Dale L Greiner, Teresa P DiLorenzo

Abstract read
In one paragraph

Article in European journal of immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

4 authors.

Nitin P AmdareDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, New York, USA.
Leonard D ShultzThe Jackson Laboratory, Bar Harbor, Maine, USA.
Dale L GreinerProgram in Molecular Medicine, Diabetes Center of Excellence, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.
Teresa P DiLorenzoDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, New York, USA.ORCID 0000-0003-4337-3598

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI Ulrich Steidl · 1985 to 2026
$111.2M
Stable Isotope and Metabolomics CoreP60DK020541 · NIDDK · YESHIVA UNIVERSITY · PI PESSIN, JEFFREY E. · 1986 to 2014
$29.8M
Humanized Mouse Avatars for T1DU01DK104218 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BREHM, MICHAEL ALLEN, GREINER, DALE LESLIE · 2019 to 2023
$4.5M
Humanized Mouse Avatars for T1DUC4DK104218 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BREHM, MICHAEL ALLEN, DALEY, GEORGE Q · 2014 to 2014
$4.1M
Structural, functional, and mechanistic anlaysis of autoreactive CD8 T cellsR01AI123730 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI ALMO, STEVEN C., DILORENZO, TERESA P · 2018 to 2022
$3.6M
The "dark immunopeptidome" as a source of CD8 T cell epitopes in type 1 diabetesR01DK135079 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI DILORENZO, TERESA P, PURCELL, ANTHONY · 2023 to 2024
$1.2M
NCI CLINICAL INVESTIGATOR AWARD PROGRAMK08CA001333 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI ANDREWS, DAVID F · 1988 to 1990
–
Diabetes Research Center of the Albert Einstein College of Medicine; and NIDDK-supported Human Islet Research Network DK104218NCI NIH HHS P30 CA013330NIAID NIH HHS R01 AI123730NIDDK NIH HHS P60 DK020541NIDDK NIH HHS R01 DK135079NIDDK NIH HHS U01 DK104218NIDDK NIH HHS UC4 DK104218NIH HHS P30 CA01333NIH HHS R01 AI123730NIH HHS R01 DK135079
6 · The paper itself

Abstract

Type 1 diabetes (T1D) is characterized by T-cell responses to islet antigens. Investigations in humans and the nonobese diabetic (NOD) mouse model of T1D have revealed that T-cell reactivity to insulin plays a central role in the autoimmune response. As there is no convenient NOD-based model to study human insulin (hIns) or its T-cell epitopes in the context of spontaneous T1D, we developed a NOD mouse strain transgenically expressing hIns in islets under the control of the human regulatory region. Female NOD.hIns mice developed T1D at approximately the same rate and overall incidence as NOD mice. Islet-infiltrating T cells from NOD.hIns mice recognized hIns peptides; both CD8 and CD4 T-cell epitopes were identified. We also demonstrate that islet-infiltrating T cells from HLA-transgenic NOD.hIns mice can be used to identify potentially patient-relevant hIns T-cell epitopes. Besides serving as an antigen, hIns was expressed in the thymus of NOD.hIns mice and could serve as a protector against T1D under certain circumstances, as previously suggested by genetic studies in humans. NOD.hIns mice and related strains facilitate human-relevant epitope discovery efforts and the investigation of fundamental questions that cannot be readily addressed in humans.

Indexed as

Diabetes Mellitus, Type 1Epitopes, T-LymphocyteInsulinIslets of LangerhansMice, Inbred NODMice, TransgenicAnimalsAutoantigensCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesFemaleHumansMiceThymus GlandAutoantigensEpitopes, T-LymphocyteInsulinAnimal modelsAutoimmunityCD8 T cellsMHCTransgenic models

Identifiers

PMID38778498
PMCPMC11563931

What Socratic 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 Socratic graph.