Evidence map›Paper›PMID 37042831›Full record

ArticleeLife2023

Transcriptome network analysis implicates CX3CR1-positive type 3 dendritic cells in non-infectious uveitis.

Sanne Hiddingh, Aridaman Pandit, Fleurieke Verhagen, Rianne Rijken, Nila Hendrika Servaas, Rina C G K Wichers, Ninette H Ten Dam-van Loon, Saskia M Imhof, Timothy R D J Radstake, Joke H de Boer and 1 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
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  9. The pyruvate-GPR31 axis promotes transepithelial dendrite formation in human intestinal dendritic cells.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  10. Review
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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 1 institution in 1 country.

Sanne Hiddingh *Ophthalmo-Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Aridaman Pandit *Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.ORCID 0000-0003-2057-9737
Fleurieke Verhagen *Ophthalmo-Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Rianne RijkenCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Nila Hendrika ServaasCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.ORCID 0000-0002-9825-7554
Rina C G K WichersCenter for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Ninette H Ten Dam-van LoonDepartment of Ophthalmology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Saskia M ImhofOphthalmo-Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Timothy R D J RadstakeUniversity Medical Center Utrecht and Utrecht University, Utrecht, Netherlands.
Joke H de BoerOphthalmo-Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Jonas J W KuiperOphthalmo-Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.ORCID 0000-0002-5370-6395
Utrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Type I interferons (IFNs) promote the expansion of subsets of CD1c+ conventional dendritic cells (CD1c+ DCs), but the molecular basis of CD1c+ DCs involvement in conditions not associated without elevated type I IFNs remains unclear. Methods: We analyzed CD1c+ DCs from two cohorts of non-infectious uveitis patients and healthy donors using RNA-sequencing followed by high-dimensional flow cytometry to characterize the CD1c+ DC populations. Results: We report that the CD1c+ DCs pool from patients with non-infectious uveitis is skewed toward a gene module with the chemokine receptor Conclusions: These results show that CX3CR1+ DC3s are implicated in non-infectious uveitis and can secrete proinflammatory mediators implicated in its pathophysiology. Funding: The presented work is supported by UitZicht (project number #2014-4, #2019-10, and #2021-4). The funders had no role in the design, execution, interpretation, or writing of the study.

Indexed as

TranscriptomeUveitisAntigens, CD1CX3C Chemokine Receptor 1CytokinesDendritic CellsFlow CytometryHumansAntigens, CD1CX3C Chemokine Receptor 1CX3CR1 protein, humanCytokinesautoimmune response/diseaseCD1cdendritic cellshumanimmunologyinflammationinterferonsmedicineRNA-sequveitis

Identifiers

PMID37042831
PMCPMC10185339
OpenAlexW4365136114

What Socratic 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 Socratic graph.