Evidence map›Paper›PMID 19289577›Full record

ArticleThe Journal of experimental medicine2009

Normally occurring NKG2D+CD4+ T cells are immunosuppressive and inversely correlated with disease activity in juvenile-onset lupus.

Zhenpeng Dai, Cameron J Turtle, Garrett C Booth, Stanley R Riddell, Theodore A Gooley, Anne M Stevens, Thomas Spies, Veronika Groh

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

70 citing papers in PubMed, 115 citations in OpenAlex.

  1. Article
  2. Article
  3. FunctionalInternational journal of molecular sciences · 2024
    Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. [Role of CD4Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2023
    Article
  9. Age as a risk factor in vasculitis.Seminars in immunopathology · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Suppressive activity of Vδ2Cancer immunology, immunotherapy : CII · 2020
    Article
  16. Article
  17. Natural killer NKG2A and NKG2D in patients with colorectal cancer.Journal of gastrointestinal oncology · 2019
    Article
  18. Article
  19. Review
  20. Regulatory NK1.1Cancer immunology, immunotherapy : CII · 2018
    Article

10 more citing papers are in PubMed but not listed here.

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 1 country.

Zhenpeng DaiFred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Cameron J Turtle
Garrett C Booth
Stanley R Riddell
Theodore A Gooley
Anne M Stevens
Thomas Spies
Veronika Groh
Fred Hutch Cancer Center · USSeattle Children's Hospital · US

Funding

Cell-Stress Induced Immune ResponsesR37AI030581 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI SPIES, THOMAS · 2001 to 2010
$5.7M
T Cell Modulation by NKG2DR01AI052319 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI SPIES, THOMAS · 2002 to 2013
$3.8M
Mechanisms of Tolerance to Renal Maternal MicrochimerismR01AR051545 · NIAMS · SEATTLE CHILDREN'S HOSPITAL · PI STEVENS, ANNE MARGUERITE · 2007 to 2011
$1.9M
NOVEL IMMUNE RESPONSE GENES WITHIN THE HUMAN MHCR01AI030581 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI SPIES, THOMAS · 1991 to 2000
$366k
NIAID NIH HHS AI30581NIAID NIH HHS AI52319NIAID NIH HHS R01 AI030581NIAID NIH HHS R01 AI052319NIAID NIH HHS R37 AI030581NIAMS NIH HHS R01 AR051545
6 · The paper itself

Abstract

The NKG2D receptor stimulates natural killer cell and T cell responses upon engagement of ligands associated with malignancies and certain autoimmune diseases. However, conditions of persistent NKG2D ligand expression can lead to immunosuppression. In cancer patients, tumor expression and shedding of the MHC class I-related chain A (MICA) ligand of NKG2D drives proliferative expansions of NKG2D(+)CD4(+) T cells that produce interleukin-10 (IL-10) and transforming growth factor-beta, as well as Fas ligand, which inhibits bystander T cell proliferation in vitro. Here, we show that increased frequencies of functionally equivalent NKG2D(+)CD4(+) T cells are inversely correlated with disease activity in juvenile-onset systemic lupus erythematosus (SLE), suggesting that these T cells may have regulatory effects. The NKG2D(+)CD4(+) T cells correspond to a normally occurring small CD4 T cell subset that is autoreactive, primed to produce IL-10, and clearly distinct from proinflammatory and cytolytic CD4 T cells with cytokine-induced NKG2D expression that occur in rheumatoid arthritis and Crohn's disease. As classical regulatory T cell functions are typically impaired in SLE, it may be clinically significant that the immunosuppressive NKG2D(+)CD4(+) T cells appear functionally uncompromised in this disease.

Indexed as

Age of OnsetAntigens, CDCD4 AntigensCD4-Positive T-LymphocytesCytokinesFetal BloodHumansImmunologic MemoryInfant, NewbornInterleukin-10Killer Cells, NaturalLupus Erythematosus, SystemicNK Cell Lectin-Like Receptor Subfamily KReference ValuesT-LymphocytesT-Lymphocyte SubsetsAntigens, CDCD4 AntigensCytokinesInterleukin-10KLRK1 protein, humanNK Cell Lectin-Like Receptor Subfamily KTransforming Growth Factor beta

Identifiers

PMID19289577
PMCPMC2715116
OpenAlexW2109244699

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.