Evidence map›Paper›PMID 25713364›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Tetramers reveal IL-17-secreting CD4+ T cells that are specific for U1-70 in lupus and mixed connective tissue disease.

Nicole H Kattah, Evan W Newell, Justin Ansel Jarrell, Alvina D Chu, Jianming Xie, Michael G Kattah, Ofir Goldberger, Jessica Ye, Eliza F Chakravarty, Mark M Davis and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-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

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. From thymus to tissues and tumors: A review of T-cell biology.The Journal of allergy and clinical immunology · 2023
    Review
  4. T cell help in the autoreactive germinal center.Scandinavian journal of immunology · 2022
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. IL-17 in Renal Immunity and Autoimmunity.Journal of immunology (Baltimore, Md. : 1950) · 2018
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Metabolic Factors that Contribute to Lupus Pathogenesis.Critical reviews in immunology · 2016
    Review
  18. Review
  19. 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

11 authors at 2 institutions in 1 country.

Nicole H KattahDivision of Immunology and Rheumatology, Department of Medicine and.
Evan W NewellDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305.
Justin Ansel JarrellDivision of Immunology and Rheumatology, Department of Medicine and.
Alvina D ChuDivision of Immunology and Rheumatology, Department of Medicine and.
Jianming XieDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305.
Michael G KattahDivision of Immunology and Rheumatology, Department of Medicine and.
Ofir GoldbergerDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305.
Jessica YeDivision of Immunology and Rheumatology, Department of Medicine and.
Eliza F ChakravartyDivision of Immunology and Rheumatology, Department of Medicine and.
Mark M DavisDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305 mmdavis@stanford.edu pjutz@stanford.edu.
Paul J UtzDivision of Immunology and Rheumatology, Department of Medicine and mmdavis@stanford.edu pjutz@stanford.edu.
Center for Rheumatology · USStanford University · US

Funding

Ultra-Fast Epigenomic Maps for Monitoring AutoimmunityU19AI110491 · NIAID · STANFORD UNIVERSITY · PI UTZ, PAUL JOSEPH · 2014 to 2018
$3.6M
NIAID NIH HHS U19 AI110491
6 · The paper itself

Abstract

Antigen-specific CD4(+) T cells are implicated in the autoimmune disease systemic lupus erythematosus (SLE), but little is known about the peptide antigens that they recognize and their precise function in disease. We generated a series of MHC class II tetramers of I-E(k)-containing peptides from the spliceosomal protein U1-70 that specifically stain distinct CD4(+) T-cell populations in MRL/lpr mice. The T-cell populations recognize an epitope differing only by the presence or absence of a single phosphate residue at position serine(140). The frequency of CD4(+) T cells specific for U1-70(131-150):I-E(k) (without phosphorylation) correlates with disease severity and anti-U1-70 autoantibody production. These T cells also express RORγt and produce IL-17A. Furthermore, the U1-70-specific CD4(+) T cells that produce IL-17A are detected in a subset of patients with SLE and are significantly increased in patients with mixed connective tissue disease. These studies provide tools for studying antigen-specific CD4(+) T cells in lupus, and demonstrate an antigen-specific source of IL-17A in autoimmune disease.

Indexed as

AnimalsAutoantibodiesCD4-Positive T-LymphocytesEnzyme-Linked Immunosorbent AssayFemaleHumansInterleukin-17Lupus Erythematosus, SystemicMaleMiceMixed Connective Tissue DiseaseOligopeptidesPhosphorylationAutoantibodiesInterleukin-17OligopeptidesautoimmunityIL-17lupusSLEtetramer

Identifiers

PMID25713364
PMCPMC4364210
OpenAlexW2028739802

What OpenQuestion holds

Textmetadata
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.