Evidence map›Paper›PMID 11178123›Full record

ReviewArthritis research2001

Cell-cell interactions in synovitis: antigen presenting cells and T cell interaction in rheumatoid arthritis.

T Aarvak, J B Natvig

Open access · diamondAbstract readReview
In one paragraph

Review in Arthritis research, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.3field-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

20 citing papers in PubMed, 62 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Mutant p53Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Observational
  11. Review
  12. RADB: a database of rheumatoid arthritis-related polymorphisms.Database : the journal of biological databases and curation · 2014
    Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Osteopontin deficiency protects joints against destruction in anti-type II collagen antibody-induced arthritis in mice.Proceedings of the National Academy of Sciences of the United States of America · 2002
    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

2 authors.

T AarvakInstitute of Immunology, Laboratory of Rheumatology Research, The National Hospital, Oslo, Norway. tanja.aarvak@labmed.uio.no
J B Natvig

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The synovial tissue in rheumatoid arthritis (RA) patients is enriched with mature antigen presenting cells (APCs) and many T lymphocytes. Interactions between APCs and T cells are essential for the initiation and amplification of T-cell-dependent immune responses, and may therefore play an important role in the chronic inflammatory processes in the synovium. The nature of the antigen(s) involved in RA still remains elusive. However, interactions and signaling through the costimulatory molecules CD28-CD80/86 and CD40-CD40L are critical during APC-T cell interaction for optimal cell activation. This review discusses how such costimulatory signals can be involved in the initiation and amplification of the inflammatory reactions in the synovium. Blocking of the signaling pathways involved in APC-T cell interactions might provide a specific immuno-therapeutic approach for the treatment of RA.

Indexed as

AnimalsAntigen PresentationAntigen-Presenting CellsArthritis, RheumatoidCell CommunicationHumansSynovitisT-Lymphocytes

Identifiers

PMID11178123
PMCPMC128879
OpenAlexW1920662684

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.