Evidence map›Paper›PMID 24127484›Full record

ArticleThe Journal of experimental medicine2013

Pathogenic CD4⁺ T cells recognizing an unstable peptide of insulin are directly recruited into islets bypassing local lymph nodes.

James F Mohan, Boris Calderon, Mark S Anderson, Emil R Unanue

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

45 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. CD4Immunity · 2024
    Article
  6. Aire mediates tolerance to insulin through thymic trimming of high-affinity T cell clones.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  7. Review
  8. Article
  9. Regulatory CD4Frontiers in immunology · 2024
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. T cell help in the autoreactive germinal center.Scandinavian journal of immunology · 2022
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  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

4 authors at 2 institutions in 1 country.

James F MohanDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110.
Boris Calderon
Mark S Anderson
Emil R Unanue
Washington University in St. Louis · USUniversity of California, San Francisco · US

Funding

WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Clay F. Semenkovich · 2013 to 2026
$27.1M
TRANSGENICS COREP60DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI SCHAFFER, JEAN E. · 1986 to 2012
$25.2M
Research BaseP30DK063720 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VAISSE, CHRISTIAN · 2003 to 2019
$21.8M
DIABETOGENIC MOLECULE I-AG7--CHEMISTRY AND BIOLOGYR01DK058177 · NIDDK · WASHINGTON UNIVERSITY · PI UNANUE, EMIL RAPHAEL · 2000 to 2020
$7.8M
ANTIGEN PRESENTATION--ROLE OF IA MOLECULESR01AI024742 · NIAID · WASHINGTON UNIVERSITY · PI UNANUE, EMIL RAPHAEL · 1997 to 2012
$6.5M
ANTIGEN PRESENTATION-ROLE OF IA MOLECULESR37AI024742 · NIAID · WASHINGTON UNIVERSITY · PI UNANUE, EMIL R · 1987 to 1996
–
NIAID NIH HHS AI024742NIAID NIH HHS R01 AI024742NIDDK NIH HHS DK058177NIDDK NIH HHS DK20579NIDDK NIH HHS P30 DK020579NIDDK NIH HHS P30 DK063720NIDDK NIH HHS P60 DK020579NIDDK NIH HHS R01 DK058177
6 · The paper itself

Abstract

In the nonobese diabetic mouse, a predominant component of the autoreactive CD4(+) T cell repertoire is directed against the B:9-23 segment of the insulin B chain. Previous studies established that the majority of insulin-reactive T cells specifically recognize a weak peptide-MHC binding register within the B:9-23 segment, that to the 12-20 register. These T cells are uniquely stimulated when the B:9-23 peptide, but not the insulin protein, is offered to antigen presenting cells (APCs). Here, we report on a T cell receptor (TCR) transgenic mouse (8F10) that offers important new insights into the biology of these unconventional T cells. Many of the 8F10 CD4(+) T cells escaped negative selection and were highly pathogenic. The T cells were directly recruited into islets of Langerhans, where they established contact with resident intra-islet APCs. Immunogenic insulin had to be presented in order for the T cells to localize and cause disease. These T cells bypassed an initial priming stage in the pancreatic lymph node thought to precede islet T cell entry. 8F10 T cells induced the production of antiinsulin antibodies and islets contained immunoglobulin (IgG) deposited on β cells and along the vessel walls.

Indexed as

Amino Acid SequenceAnimalsCD4-Positive T-LymphocytesFemaleInsulinIslets of LangerhansLymph NodesMiceMice, Inbred NODMice, TransgenicMolecular Sequence DataPeptidesProtein StabilityReceptors, Antigen, T-CellInsulinPeptidesReceptors, Antigen, T-Cell

Identifiers

PMID24127484
PMCPMC3804950
OpenAlexW2101620717

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.