Evidence map›Paper›PMID 27428460›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2017

Brief Report: Altered Innate Lymphoid Cell Subsets in Human Lymph Node Biopsy Specimens Obtained During the At-Risk and Earliest Phases of Rheumatoid Arthritis.

Javier Rodríguez-Carrio, Janine S Hähnlein, Tamara H Ramwadhdoebe, Johanna F Semmelink, Ivy Y Choi, Krijn P van Lienden, Mario Maas, Danielle M Gerlag, Paul P Tak, Teunis B H Geijtenbeek and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. ILC3: a case of conflicted identity.Frontiers in immunology · 2023
    Review
  11. Rheumatoid Arthritis: Pathogenic Roles of Diverse Immune Cells.International journal of molecular sciences · 2022
    Review
  12. Review
  13. The gut-joint axis in rheumatoid arthritis.Nature reviews. Rheumatology · 2021
    Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Innate Lymphoid Cells in Autoimmune Diseases.Frontiers in immunology · 2021
    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

11 authors at 2 institutions in 2 countries.

Javier Rodríguez-CarrioAcademic Medical Center, University of Amsterdam, Amsterdam, The Netherlands, and University of Oviedo, Asturias, Spain.
Janine S HähnleinAcademic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Tamara H RamwadhdoebeAcademic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Johanna F SemmelinkAcademic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Ivy Y ChoiAcademic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Krijn P van LiendenAcademic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Mario MaasAcademic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Danielle M GerlagAcademic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Paul P TakAcademic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Teunis B H GeijtenbeekAcademic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Lisa G M van BaarsenAcademic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
University of Amsterdam · NLAcademic Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveInnate lymphoid cells (ILCs) are emerging mediators of immunity, and accumulation of inflammatory ILC populations can occur in inflammatory-mediated conditions. Since early lymph node (LN) activation has been shown in rheumatoid arthritis (RA), we aimed to investigate the frequency and distribution of ILCs in LN biopsy specimens obtained during the earliest phases of RA.

methodsTwelve patients with early RA, 12 individuals with IgM rheumatoid factor and/or anti-citrullinated protein antibodies without arthritis (RA risk group), and 7 healthy controls underwent ultrasound-guided inguinal LN biopsy. ILC subsets and the expression of vascular cell adhesion molecule (VCAM) and intercellular adhesion molecule (ICAM) by LN endothelial cells and fibroblasts were analyzed by flow cytometry.

resultsAlthough no differences in the frequencies of total ILCs (Lin-CD45

conclusionOur findings indicate that during the at-risk and earliest phases of RA, the ILC distribution in LN changes from a homeostatic profile toward a more inflammatory profile, thereby providing evidence of a role for ILCs in RA pathogenesis.

Indexed as

LymphocytesAdultArthritis, RheumatoidBiopsyFemaleHumansLymph NodesMaleMiddle AgedRisk FactorsSeverity of Illness Index

Identifiers

PMID27428460
PMCPMC6681066
OpenAlexW2578463312

What OpenQuestion holds

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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.