Evidence map›Paper›PMID 33015599›Full record

ArticleJournal of translational autoimmunity2020

cDC1 are required for the initiation of collagen-induced arthritis.

Maria Ines Ramos, Samuel Garcia, Boy Helder, Saida Aarrass, Kris A Reedquist, Sten E Jacobsen, Paul Peter Tak, Maria Cristina Lebre

Open access · goldAbstract read
In one paragraph

Article in Journal of translational autoimmunity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. CD11c-Cre driven deletion ofFrontiers in immunology · 2025
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  3. Article
  4. Review
  5. 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

8 authors at 3 institutions in 2 countries.

Maria Ines RamosDepartment of Clinical Immunology and Rheumatology.
Samuel GarciaDepartment of Clinical Immunology and Rheumatology.
Boy HelderDepartment of Clinical Immunology and Rheumatology.
Saida AarrassDepartment of Clinical Immunology and Rheumatology.
Kris A ReedquistDepartment of Clinical Immunology and Rheumatology.
Sten E JacobsenHaematopoietic Stem Cell Laboratory and MRC Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford, UK.
Paul Peter TakDepartment of Clinical Immunology and Rheumatology.
Maria Cristina LebreDepartment of Clinical Immunology and Rheumatology.
Academic Medical Center · NLUniversity of Amsterdam · NLJohn Radcliffe Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is chronic autoimmune disease which etiology remains unknown. Several cell types have been described to potentiate/aggravate the arthritic process however the initiating event in synovial inflammation is still elusive. Dendritic cells (DCs) are essential for the initiation of primary immune responses and thus we hypothesized that these cells might be crucial for RA induction. DCs are a heterogeneous population of cells comprising different subsets with distinct phenotype and function. Here we investigated which DC subset(s) is/are crucial for the initiation of the arthritic process. We have previously demonstrated that Flt3-/- mice, with reduced DCs, were protected from collagen induced arthritis (CIA). Here we have shown that GM-CSF derived DCs in Flt3L-/- mice are functional but not sufficient to induce arthritis. Batf3

Indexed as

AutoimmunitycDC1Dendritic cellsInflammation

Identifiers

PMID33015599
PMCPMC7522802
OpenAlexW3084498128

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.