Evidence map›Paper›PMID 27139492›Full record

ArticleThe Journal of experimental medicine2016

Class-switched anti-insulin antibodies originate from unconventional antigen presentation in multiple lymphoid sites.

Xiaoxiao Wan, James W Thomas, Emil R Unanue

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

35 citing papers in PubMed, 45 citations in OpenAlex.

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  14. Endotypes in T1D: B lymphocytes and early onset.Current opinion in endocrinology, diabetes, and obesity · 2020
    Review
  15. Review
  16. Article
  17. Review
  18. Programmed Death-1 Restrains the Germinal Center in Type 1 Diabetes.Journal of immunology (Baltimore, Md. : 1950) · 2019
    Article
  19. 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

3 authors at 2 institutions in 1 country.

Xiaoxiao WanDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110.
James W ThomasDepartment of Medicine, Vanderbilt University Medical School, Nashville, TN 37232.
Emil R UnanueDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110 unanue@wustl.edu.
Washington University in St. Louis · USVanderbilt University · US

Funding

WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Jennifer Lynn Powers Carson · 2013 to 2026
$27.1M
TRANSGENICS COREP60DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI SCHAFFER, JEAN E. · 1986 to 2012
$25.2M
DIABETOGENIC MOLECULE I-AG7--CHEMISTRY AND BIOLOGYR01DK058177 · NIDDK · WASHINGTON UNIVERSITY · PI UNANUE, EMIL RAPHAEL · 2000 to 2020
$7.8M
Selection &Regulation of B Lymphocytes in IDDMR01AI051448 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BONAMI, RACHEL H · 2003 to 2022
$7.3M
AUTOIMMUNE DIABETES: EARLY EVENTS IN ISLETS OF LANGERHANSR01AI114551 · NIAID · WASHINGTON UNIVERSITY · PI UNANUE, EMIL RAPHAEL · 2015 to 2019
$2.1M
T Follicular Helper Cells and Type 1 DiabetesR21DK091692 · NIDDK · VANDERBILT UNIVERSITY · PI THOMAS, JAMES W · 2011 to 2012
$429k
Selection &Regulation of B Lymphocytes in IDDMR21AI051448 · NIAID · VANDERBILT UNIVERSITY · PI THOMAS, JAMES WARD · 2003 to 2003
$138k
NIAID NIH HHS R01 AI051448NIAID NIH HHS R01 AI114551NIAID NIH HHS R21 AI051448NIDDK NIH HHS P30 DK020579NIDDK NIH HHS P60 DK020579NIDDK NIH HHS R01 DK058177NIDDK NIH HHS R21 DK091692
6 · The paper itself

Abstract

Autoantibodies to insulin are a harbinger of autoimmunity in type 1 diabetes in humans and in non-obese diabetic mice. To understand the genesis of these autoantibodies, we investigated the interactions of insulin-specific T and B lymphocytes using T cell and B cell receptor transgenic mice. We found spontaneous anti-insulin germinal center (GC) formation throughout lymphoid tissues with GC B cells binding insulin. Moreover, because of the nature of the insulin epitope recognized by the T cells, it was evident that GC B cells presented a broader repertoire of insulin epitopes. Such broader recognition was reproduced by activating naive B cells ex vivo with a combination of CD40 ligand and interleukin 4. Thus, insulin immunoreactivity extends beyond the pancreatic lymph node-islets of Langerhans axis and indicates that circulating insulin, despite its very low levels, can have an influence on diabetogenesis.

Indexed as

AnimalsAntigen PresentationB-LymphocytesCD40 AntigensDiabetes Mellitus, Type 1Germinal CenterImmunoglobulin Class SwitchingInsulinInterleukin-4Islets of LangerhansMiceMice, KnockoutT-LymphocytesCD40 AntigensInsulinInterleukin-4

Identifiers

PMID27139492
PMCPMC4886365
OpenAlexW2345459561

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.