Evidence map›Paper›PMID 37792335›Full record

ArticleInvestigative ophthalmology & visual science2023

CRB1-Associated Retinal Dystrophy Patients Have Expanded Lewis Glycoantigen-Positive T Cells.

Lude Moekotte, Jonas J W Kuiper, Sanne Hiddingh, Xuan-Thanh-An Nguyen, Camiel J F Boon, L Ingeborgh van den Born, Joke H de Boer, Maria M van Genderen

Open access · goldAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Metabolomic signatures suggest altered bile acid and energy metabolism in CRB1- retinopathies.Metabolomics : Official journal of the Metabolomic Society · 2026
    Article
  2. Article
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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

8 authors at 3 institutions in 1 country.

Lude MoekotteDepartment of Ophthalmology, University Medical Center Utrecht, Utrecht, the Netherlands.
Jonas J W KuiperDepartment of Ophthalmology, University Medical Center Utrecht, Utrecht, the Netherlands.
Sanne HiddinghDepartment of Ophthalmology, University Medical Center Utrecht, Utrecht, the Netherlands.
Xuan-Thanh-An NguyenDepartment of Ophthalmology, Leiden University Medical Center, Leiden, the Netherlands.
Camiel J F BoonDepartment of Ophthalmology, Leiden University Medical Center, Leiden, the Netherlands.
L Ingeborgh van den BornThe Rotterdam Eye Hospital and Rotterdam Ophthalmic Institute, Rotterdam, the Netherlands.
Joke H de BoerDepartment of Ophthalmology, University Medical Center Utrecht, Utrecht, the Netherlands.
Maria M van GenderenDepartment of Ophthalmology, University Medical Center Utrecht, Utrecht, the Netherlands.
University Medical Center Utrecht · NLLeiden University Medical Center · NLRotterdam Eye Hospital · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Eye inflammation may occur in patients with inherited retinal dystrophies (IRDs) and is seen frequently in IRDs associated with mutations in the CRB1 gene. The purpose of this study was to determine the types of inflammatory cells involved in IRDs, by deep profiling the composition of peripheral blood mononuclear cells of patients with a CRB1-associated IRD. Methods: This study included 33 patients with an IRD with confirmed CRB1 mutations and 32 healthy controls. A 43-parameter flow cytometry analysis was performed on peripheral blood mononuclear cells isolated from venous blood. FlowSOM and manual Boolean combination gating were used to identify and quantify immune cell subsets. Results: Comparing patients with controls revealed a significant increase in patients in the abundance of circulating CD4+ T cells and CD8+ T cells that express sialyl Lewis X antigen. Furthermore, we detected a decrease in plasmacytoid dendritic cells and an IgA+CD24+CD38+ transitional B-cell subset in patients with an IRD. Conclusions: Patients with a CRB1-associated IRD show marked changes in blood leukocyte composition, affecting lymphocyte and dendritic cell populations. These results implicate inflammatory pathways in the disease manifestations of IRDs.

Indexed as

Eye AbnormalitiesRetinal DystrophiesEye ProteinsHumansLeukocytes, MononuclearMembrane ProteinsMutationNerve Tissue ProteinsT-LymphocytesCRB1 protein, humanEye ProteinsMembrane ProteinsNerve Tissue Proteins

Identifiers

PMID37792335
PMCPMC10565706
OpenAlexW4387325948

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.