Evidence map›Paper›PMID 25505281›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2015

Antigen recognition in the islets changes with progression of autoimmune islet infiltration.

Robin S Lindsay, Kaitlin Corbin, Ashley Mahne, Bonnie E Levitt, Matthew J Gebert, Eric J Wigton, Brenda J Bradley, Kathryn Haskins, Jordan Jacobelli, Qizhi Tang and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  14. Immune cell trafficking to the islets during type 1 diabetes.Clinical and experimental immunology · 2019
    Review
  15. Article
  16. CD11cFrontiers in immunology · 2019
    Article
  17. Article
  18. Article
  19. Imaging the emergence and natural progression of spontaneous autoimmune diabetes.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  20. 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

12 authors at 3 institutions in 1 country.

Robin S LindsayDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206; Department of Immunology and Microbiology, University of Colorado School of Medicine, Denver, CO 80206;
Kaitlin CorbinDepartment of Pathology, University of California San Francisco, San Francisco, CA 94143; and.
Ashley MahneDepartment of Surgery, University of California San Francisco, San Francisco, CA 94143.
Bonnie E LevittDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206;
Matthew J GebertDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206;
Eric J WigtonDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206;
Brenda J BradleyDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206; Department of Immunology and Microbiology, University of Colorado School of Medicine, Denver, CO 80206;
Kathryn HaskinsDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206; Department of Immunology and Microbiology, University of Colorado School of Medicine, Denver, CO 80206;
Jordan JacobelliDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206; Department of Immunology and Microbiology, University of Colorado School of Medicine, Denver, CO 80206;
Qizhi TangDepartment of Surgery, University of California San Francisco, San Francisco, CA 94143.
Matthew F KrummelDepartment of Pathology, University of California San Francisco, San Francisco, CA 94143; and.
Rachel S FriedmanDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206; Department of Immunology and Microbiology, University of Colorado School of Medicine, Denver, CO 80206; FriedmanR@NJHealth.org.
National Jewish Health · USUniversity of California, San Francisco · USUniversity of Colorado Denver · US

Funding

Understanding Asthma EndotypesU19AI077439 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI David J Erle · 2008 to 2026
$41.1M
Tools for Analysis of Airway InflammationP01HL024136 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRUMMEL, MATTHEW F · 1985 to 2014
$23.3M
Research BaseP30DK063720 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRUMMEL, MATTHEW F · 2003 to 2019
$21.8M
MOLECULAR AND CELLULAR IMMUNOLOGYT32AI007334 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CYSTER, JASON G · 1988 to 2023
$11.0M
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
"Regulatory 'T' Cell Control of Autoimmune Diabetes".R01DK085231 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI TANG, QIZHI · 2010 to 2014
$1.6M
NHLBI NIH HHS P01 HL024136NIAID NIH HHS T32 AI007334NIAID NIH HHS U19 AI077439NIDDK NIH HHS P30 DK063720NIDDK NIH HHS R01 DK081166NIDDK NIH HHS R01 DK08231NIDDK NIH HHS R01 DK085231
6 · The paper itself

Abstract

In type 1 diabetes, the pancreatic islets are an important site for therapeutic intervention because immune infiltration of the islets is well established at diagnosis. Therefore, understanding the events that underlie the continued progression of the autoimmune response and islet destruction is critical. Islet infiltration and destruction is an asynchronous process, making it important to analyze the disease process on a single islet basis. To understand how T cell stimulation evolves through the process of islet infiltration, we analyzed the dynamics of T cell movement and interactions within individual islets of spontaneously autoimmune NOD mice. Using both intravital and explanted two-photon islet imaging, we defined a correlation between increased islet infiltration and increased T cell motility. Early T cell arrest was Ag dependent and due, at least in part, to Ag recognition through sustained interactions with CD11c(+) APCs. As islet infiltration progressed, T cell motility became Ag independent, with a loss of T cell arrest and sustained interactions with CD11c(+) APCs. These studies suggest that the autoimmune T cell response in the islets may be temporarily dampened during the course of islet infiltration and disease progression.

Indexed as

AnimalsAntigen-Presenting CellsAutoantigensCD11c AntigenCell MovementDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Islets of LangerhansMiceMice, Inbred NODMice, TransgenicT-LymphocytesAutoantigensCD11c Antigen

Identifiers

PMID25505281
PMCPMC4282963
OpenAlexW2152428556

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.