Evidence map›Paper›PMID 26566677›Full record

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

γδ T Cell-Dependent Regulatory T Cells Prevent the Development of Autoimmune Keratitis.

Yafei Huang, Zhifang Yang, Chunjian Huang, Jessica McGowan, Tamara Casper, Deming Sun, Willi K Born, Rebecca L O'Brien

Open access · bronzeAbstract 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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Treg cells require Izumo1R to regulate γδT cell-driven inflammation in the skin.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Bilateral Sterile Pyogranulomatous Keratitis in a Dog.Case reports in veterinary medicine · 2019
    Article
  8. Article
  9. Association of Decreased Percentage of Vδ2Frontiers in immunology · 2018
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Autoimmunity in 2015.Clinical reviews in allergy & immunology · 2016
    Review
  16. 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

8 authors at 2 institutions in 2 countries.

Yafei HuangDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206; Department of Immunology and Microbiology, University of Colorado Denver School of Medicine, Aurora, CO 80045; Joint Laboratory for Stem Cell Engineering and Technology Transfer, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan City 430030, People's Republic of China;
Zhifang YangDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206; Department of Immunology and Microbiology, University of Colorado Denver School of Medicine, Aurora, CO 80045; Department of Breast and Thyroid Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan City 430030, People's Republic of China; and.ORCID http://orcid.org/0000-0003-2400-7488
Chunjian HuangDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206;
Jessica McGowanDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206;
Tamara CasperDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206;
Deming SunDoheny Eye Institute, Department of Ophthalmology, University of Southern California, Los Angeles, CA 90033.ORCID http://orcid.org/0000-0003-4851-0416
Willi K BornDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206; Department of Immunology and Microbiology, University of Colorado Denver School of Medicine, Aurora, CO 80045;
Rebecca L O'BrienDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206; Department of Immunology and Microbiology, University of Colorado Denver School of Medicine, Aurora, CO 80045; obrienr@njhealth.org.
National Jewish Health · USUniversity of Southern California · US

Funding

TRAINING PROGRAM IN IMMUNOLOGYT32AI007405 · NIAID · UNIVERSITY OF COLORADO DENVER · PI Laurel L Lenz, Raul Martin Torres · 1991 to 2026
$10.5M
Role of IL-17+ Autoreactive T Cells in Experimental Autoimmune Uveitis (EAU)R01EY018827 · NEI · DOHENY EYE INSTITUTE · PI SUN, DEMING · 2009 to 2023
$4.8M
Regulation by Gammadelta T Cells of Autoimmune Uveitis (EAU)R01EY022403 · NEI · DOHENY EYE INSTITUTE · PI SUN, DEMING · 2012 to 2015
$1.6M
Gamma/delta T cells in autoimmune keratitisR01EY021199 · NEI · NATIONAL JEWISH HEALTH · PI O'BRIEN, REBECCA L. · 2012 to 2015
$1.5M
NEI NIH HHS R01 EY018827NEI NIH HHS R01 EY021199NEI NIH HHS R01EY021199NEI NIH HHS R01 EY022403NIAID NIH HHS T32 AI007405NIAID NIH HHS T32AI007405
6 · The paper itself

Abstract

To prevent potentially damaging inflammatory responses, the eye actively promotes local immune tolerance via a variety of mechanisms. Owing to trauma, infection, or other ongoing autoimmunity, these mechanisms sometimes fail, and an autoimmune disorder may develop in the eye. In mice of the C57BL/10 (B10) background, autoimmune keratitis often develops spontaneously, particularly in the females. Its incidence is greatly elevated in the absence of γδ T cells, such that ∼80% of female B10.TCRδ(-/-) mice develop keratitis by 18 wk of age. In this article, we show that CD8(+) αβ T cells are the drivers of this disease, because adoptive transfer of CD8(+), but not CD4(+), T cells to keratitis-resistant B10.TCRβ/δ(-/-) hosts induced a high incidence of keratitis. This finding was unexpected because in other autoimmune diseases, more often CD4(+) αβ T cells, or both CD4(+) and CD8(+) αβ T cells, mediate the disease. Compared with wild-type B10 mice, B10.TCRδ(-/-) mice also show increased percentages of peripheral memory phenotype CD8(+) αβ T cells, along with an elevated frequency of CD8(+) αβ T cells biased to produce inflammatory cytokines. In addition, B10.TCRδ-/- mice have fewer peripheral CD4(+) CD25(+) Foxp3(+) αβ regulatory T cells (Tregs), which express lower levels of receptors needed for Treg development and function. Together, these observations suggest that in B10 background mice, γδ T cells are required to generate adequate numbers of CD4(+) CD25(+) Foxp3(+) Tregs, and that in B10.TCRδ(-/-) mice a Treg deficiency allows dysregulated effector or memory CD8(+) αβ T cells to infiltrate the cornea and provoke an autoimmune attack.

Indexed as

AnimalsAutoimmune DiseasesCD8-Positive T-LymphocytesCorneaDisease ProgressionFemaleForkhead Transcription FactorsImmunologic MemoryInterleukin-2 Receptor alpha SubunitKeratitisMiceMice, Inbred C57BLMice, KnockoutReceptors, Antigen, T-Cell, alpha-betaReceptors, Antigen, T-Cell, gamma-deltaT-Lymphocytes, RegulatoryForkhead Transcription FactorsFoxp3 protein, mouseInterleukin-2 Receptor alpha SubunitReceptors, Antigen, T-Cell, alpha-betaReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID26566677
PMCPMC4670787
OpenAlexW2262741309

What OpenQuestion holds

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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.