Evidence map›Paper›PMID 35320625›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2022

Peripheral γδ T Cells Regulate Neutrophil Expansion and Recruitment in Experimental Psoriatic Arthritis.

Cuong Thach Nguyen, Hiroki Furuya, Dayasagar Das, Alina I Marusina, Alexander A Merleev, Resmi Ravindran, Zahra Jalali, Imran H Khan, Emanual Maverakis, Iannis E Adamopoulos

Open access · greenAbstract read
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. [Role of Trained Immunity in the Association Between Periodontitis and Rheumatoid Arthritis].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2025
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. IL-23 induces CLEC5AJournal of autoimmunity · 2024
    Article
  12. Article
  13. Article
  14. γδ T cells: origin and fate, subsets, diseases and immunotherapy.Signal transduction and targeted therapy · 2023
    Review
  15. Innate immune memory in inflammatory arthritis.Nature reviews. Rheumatology · 2023
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
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

10 authors at 2 institutions in 1 country.

Cuong Thach NguyenUniversity of California, Davis.ORCID 0000-0002-1894-3811
Hiroki FuruyaHarvard Medical School, Boston, Massachusetts.ORCID 0000-0002-2288-923X
Dayasagar DasUniversity of California, Davis.
Alina I MarusinaUniversity of California, Davis.
Alexander A MerleevUniversity of California, Davis.
Resmi RavindranUniversity of California, Davis.
Zahra JalaliHarvard Medical School, Boston, Massachusetts.
Imran H KhanUniversity of California, Davis.
Emanual MaverakisUniversity of California, Davis.
Iannis E AdamopoulosUniversity of California, Davis, and Harvard Medical School, Boston, Massachusetts.ORCID 0000-0002-3708-2965
University of California, Davis · USHarvard University · US

Funding

The IL-23/IL-17 Axis in Inflammatory ArthritisR01AR062173 · NIAMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LEVY, DAN · 2012 to 2025
$4.9M
NIAMS NIH HHS R01 AR062173
6 · The paper itself

Abstract

objectiveThis study was undertaken to identify the mechanistic role of γδ T cells in the pathogenesis of experimental psoriatic arthritis (PsA).

methodsIn this study, we performed interleukin-23 (IL-23) gene transfer in wild-type (WT) and T cell receptor δ-deficient (TCRδ

resultsWe demonstrated that γδ T cells support systemic granulopoiesis, which is critical for murine PsA-like pathology. Briefly, γδ T cell ablation inhibited the expression of neutrophil chemokines CXCL1 and CXCL2 and neutrophil CD11b+Ly6G+ accumulation in the aforementioned PsA-related tissues. Although significantly reduced expression of granulocyte-macrophage colony-stimulating factor (GM-CSF) and IL-17A was detected systemically in TCRδ

conclusionOur findings do not support the notion that tissue-resident γδ T cells initiate the disease but demonstrate a novel role of γδ T cells in neutrophil regulation that can be exploited therapeutically in PsA patients.

Indexed as

Arthritis, ExperimentalArthritis, PsoriaticAnimalsHumansInterleukin-17MiceMice, Inbred C57BLNeutrophilsReceptors, Antigen, T-Cell, gamma-deltaInterleukin-17Receptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID35320625
PMCPMC9427669
OpenAlexW4220832220

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.