Evidence map›Paper›PMID 29950508›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2018

Anti-Insulin B Cells Are Poised for Antigen Presentation in Type 1 Diabetes.

Jamie L Felton, Damian Maseda, Rachel H Bonami, Chrys Hulbert, James W Thomas

Open access · greenAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

28 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Altered B cell metabolic pathways characterize type 1 diabetes progression.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Article
  5. Article
  6. Article
  7. Review
  8. CD4Immunity · 2024
    Article
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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

5 authors at 2 institutions in 1 country.

Jamie L FeltonDivision of Pediatric Endocrinology, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN 37232.
Damian MasedaDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University, Nashville, TN 37232; and.ORCID 0000-0003-0722-6881
Rachel H BonamiDivision of Rheumatology and Immunology, Department of Medicine, Vanderbilt University, Nashville, TN 37232.
Chrys HulbertDivision of Rheumatology and Immunology, Department of Medicine, Vanderbilt University, Nashville, TN 37232.
James W ThomasDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University, Nashville, TN 37232; and james.w.thomas@vumc.org.ORCID 0000-0002-2098-6458
Vanderbilt University · USVanderbilt University Medical Center · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
Building Interdisciplinary Research Careers in Women's HealthK12HD043483 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HARTMANN, KATHERINE E, MAJOR, AMY S · 2002 to 2023
$10.3M
Selection &Regulation of B Lymphocytes in IDDMR01AI051448 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BONAMI, RACHEL H · 2003 to 2022
$7.3M
Conducting Child Health Care Research in Vulnerable PopulationsT32HD060554 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BARKIN, SHARI, WILLIAMS, DEREK J. · 2009 to 2019
$3.8M
NCATS NIH HHS UL1 TR000445NCI NIH HHS P30 CA068485NIAID NIH HHS R01 AI051448NICHD NIH HHS K12 HD043483NICHD NIH HHS T32 HD060554NIDDK NIH HHS U24 DK059637
6 · The paper itself

Abstract

Early breaches in B cell tolerance are central to type 1 diabetes progression in mouse and man. Conventional BCR transgenic mouse models (VH125.Tg NOD) reveal the power of B cell specificity to drive disease as APCs. However, in conventional fixed IgM models, comprehensive assessment of B cell development is limited. To provide more accurate insight into the developmental and functional fates of anti-insulin B cells, we generated a new NOD model (V

Indexed as

AnimalsAntigen PresentationAutoantibodiesAutoantigensB-Lymphocyte SubsetsDiabetes Mellitus, Type 1FemaleImmune ToleranceInflammationInsulinInsulin AntibodiesLymphocyte ActivationMaleMiceMice, Inbred NODMice, TransgenicAutoantibodiesAutoantigensInsulinInsulin AntibodiesReceptors, Antigen, B-Cell

Identifiers

PMID29950508
PMCPMC7029791
OpenAlexW2810705934

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.