Evidence map›Paper›PMID 20181889›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

FoxP3+RORgammat+ T helper intermediates display suppressive function against autoimmune diabetes.

Danielle M Tartar, Amie M VanMorlan, Xiaoxiao Wan, F Betul Guloglu, Renu Jain, Cara L Haymaker, Jason S Ellis, Christine M Hoeman, Jason A Cascio, Mermagya Dhakal and 2 more

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing 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

48 citing papers in PubMed.

  1. Frontiers in immunology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. ApoB-Specific CD4Cells · 2021
    Review
  10. Review
  11. Roles of Porphyromonas gingivalis and its virulence factors in periodontitis.Advances in protein chemistry and structural biology · 2020
    Review
  12. Article
  13. Review
  14. Thymus-derived Foxp3Journal of molecular medicine (Berlin, Germany) · 2018
    Article
  15. Article
  16. Generation of RORγtCell reports · 2017
    Article
  17. On the Role IL-4/IL-13 Heteroreceptor Plays in Regulation of Type 1 Diabetes.Journal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  18. Human IL-6RClinical immunology (Orlando, Fla.) · 2017
    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

12 authors.

Danielle M TartarDepartment of Molecular Microbiology and Immunology, University of Missouri School of Medicine, Columbia, MO 65212, USA.
Amie M VanMorlan
Xiaoxiao Wan
F Betul Guloglu
Renu Jain
Cara L Haymaker
Jason S Ellis
Christine M Hoeman
Jason A Cascio
Mermagya Dhakal
Mohamed Oukka
Habib Zaghouani

Funding

MOLECULAR BASIS OF GENE EXPRESSION AND SIGNAL PROCESSINGT32GM008396 · NIGMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI HANNINK, MARK · 1991 to 2021
$4.1M
Trafficking and the role of myelin specific Regulatory T cells in EAER01AI073542 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI OUKKA, MOHAMED · 2007 to 2011
$2.2M
T regulatory cells in type I diabetesR01DK093515 · NIDDK · UNIVERSITY OF MISSOURI-COLUMBIA · PI ZAGHOUANI, HABIB · 2012 to 2015
$1.3M
Immune Tolerance Against Type I Diabetes in MiceR01DK065748 · NIDDK · UNIVERSITY OF MISSOURI-COLUMBIA · PI ZAGHOUANI, HABIB · 2005 to 2007
$741k
Mimotopes Against Type 1 DiabetesR21AI068746 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI ZAGHOUANI, HABIB · 2007 to 2008
$405k
NIAID NIH HHS R01 AI073542NIAID NIH HHS R21 AI068746NIAID NIH HHS R21AI68746NIDDK NIH HHS R01 DK065748NIDDK NIH HHS R01 DK093515NIDDK NIH HHS R01DK65748NIGMS NIH HHS GM008396NIGMS NIH HHS T32 GM008396
6 · The paper itself

Abstract

Recently, traces of double-positive FoxP3(+)RORgammat(+) T cells were identified and viewed as dual programming differentiation intermediates geared toward development into T regulatory or Th17 cells. In this study, we report that FoxP3(+)RORgammat(+) intermediates arise in the NOD mouse T cell repertoire prior to inflammation and can be expanded with tolerogen without further differentiation. Furthermore, FoxP3(+)RORgammat(+) cells express both CD62L and membrane-bound TGFbeta and use the former to traffic to the pancreas and the latter to suppress effector T cells both in vitro and in vivo. The cells perform these functions as FoxP3(+)RORgammat(+) intermediates, despite being able to terminally differentiate into either FoxP3(+)RORgammat(-) T regulatory or FoxP3(-)RORgammat(+) Th17 cells on polarization. These previously unrecognized observations extend plasticity to both differentiation and function and indicate that the intermediates are poised to traffic to sites of inflammation and target diverse pathogenic T cells, likely without prior conditioning by effector T cells, thus broadening efficacy against autoimmunity.

Indexed as

AnimalsCell DifferentiationCell SeparationDiabetes Mellitus, Type 1Flow CytometryForkhead Transcription FactorsInterleukin-17Lymphocyte ActivationMiceMice, Inbred NODNuclear Receptor Subfamily 1, Group F, Member 3Reverse Transcriptase Polymerase Chain ReactionT-Lymphocytes, Helper-InducerT-Lymphocyte SubsetsForkhead Transcription FactorsFoxp3 protein, mouseInterleukin-17Nuclear Receptor Subfamily 1, Group F, Member 3

Identifiers

PMID20181889
PMCPMC2843758

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.