Evidence map›Paper›PMID 30717755›Full record

ArticleArthritis research & therapy2019

Tolerogenic XCR1

Kétia Ermoza, Simon Glatigny, Nadège Jah, Vânia Camilo, Hendrick Mambu Mambueni, Luiza M Araujo, Gilles Chiocchia, Maxime Breban

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Lessons on SpA pathogenesis from animal models.Seminars in immunopathology · 2021
    Review
  8. 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

8 authors at 4 institutions in 1 country.

Kétia ErmozaINSERM U1173, UFR Simone Veil, Versailles-Saint-Quentin University, 2 avenue de la source de la Bièvre, 78190, Montigny le Bretonneux, France.
Simon GlatignyINSERM U1173, UFR Simone Veil, Versailles-Saint-Quentin University, 2 avenue de la source de la Bièvre, 78190, Montigny le Bretonneux, France.
Nadège JahINSERM U1173, UFR Simone Veil, Versailles-Saint-Quentin University, 2 avenue de la source de la Bièvre, 78190, Montigny le Bretonneux, France.
Vânia CamiloINSERM U1173, UFR Simone Veil, Versailles-Saint-Quentin University, 2 avenue de la source de la Bièvre, 78190, Montigny le Bretonneux, France.
Hendrick Mambu MambueniINSERM U1173, UFR Simone Veil, Versailles-Saint-Quentin University, 2 avenue de la source de la Bièvre, 78190, Montigny le Bretonneux, France.
Luiza M AraujoINSERM U1173, UFR Simone Veil, Versailles-Saint-Quentin University, 2 avenue de la source de la Bièvre, 78190, Montigny le Bretonneux, France.
Gilles ChiocchiaINSERM U1173, UFR Simone Veil, Versailles-Saint-Quentin University, 2 avenue de la source de la Bièvre, 78190, Montigny le Bretonneux, France.
Maxime BrebanINSERM U1173, UFR Simone Veil, Versailles-Saint-Quentin University, 2 avenue de la source de la Bièvre, 78190, Montigny le Bretonneux, France. maxime.breban@aphp.fr.
Inserm · FRSorbonne Paris Cité · FRUniversité de Versailles Saint-Quentin-en-Yvelines · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSpondyloarthritis (SpA) is a chronic inflammatory disease affecting primarily axial and peripheral joints and sometimes also extra-articular organs, such as the gut. Rats transgenic for HLA-B27 and human β2-microglobulin (B27-Tg rat) develop clinical manifestations resembling human disease. In this model, it has been shown that CD103

methodscDC populations were isolated from the spleen, mesenteric lymph nodes (MLN), and colonic lamina propria from B27-TG and control nontransgenic (NTG) and/or HLA-B7 transgenic rats after collagenase digestion and density gradient and characterized with flow cytometry or real-time PCR. Migration of cDCs from intestinal mucosa to MLN was assessed, using TLR-7 stimulation with Resiquimod.

resultsWe observed a reduced frequency of cCD4

conclusionOur results demonstrate for the first time a decreased proportion of the tolerogenic XCR1

Indexed as

AnimalsAntigens, CDbeta 2-MicroglobulinCell MovementCells, CulturedDendritic CellsDisease Models, AnimalHLA-B27 AntigenHumansImmune ToleranceInflammationIntegrin alpha ChainsRats, Inbred F344Rats, TransgenicReceptors, ChemokineSpondylarthritisalpha E integrinsAntigens, CDbeta 2-MicroglobulinHLA-B27 AntigenIntegrin alpha ChainsReceptors, ChemokineXCR1 protein, ratAnkylosing spondylitisDendritic cellHLA-B27RatSpondyloarthritisXCR1

Identifiers

PMID30717755
PMCPMC6360689
OpenAlexW2919541020

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.