Evidence map›Paper›PMID 37230761›Full record

ArticleRMD open2023

Alteration of innate lymphoid cell homeostasis mainly concerns salivary glands in primary Sjögren's syndrome.

Lou Kawka, Renaud Felten, Cédric Schleiss, Jean-Daniel Fauny, Pauline Le Van Quyen, Hélène Dumortier, Fanny Monneaux, Jacques-Eric Gottenberg

Open access · goldAbstract read
In one paragraph

Article in RMD open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. ILC3: a case of conflicted identity.Frontiers in immunology · 2023
    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 2 institutions in 1 country.

Lou Kawka *Service de rhumatologie, Centre National de Référence des Maladies Autoimmunes et Systémiques Rares, Hôpitaux universitaires de Strasbourg, Strasbourg, France.
Renaud Felten *Service de rhumatologie, Centre National de Référence des Maladies Autoimmunes et Systémiques Rares, Hôpitaux universitaires de Strasbourg, Strasbourg, France renaud.felten@chru-strasbourg.fr jacques-eric.gottenberg@chru-strasbourg.fr.ORCID 0000-0002-4951-4032
Cédric SchleissLaboratoire d'Immunologie, Immunopathologie et Chimie Thérapeutique, CNRS UPR3572, Institut de Biologie Moléculaire et Cellulaire, Strasbourg, France.
Jean-Daniel FaunyLaboratoire d'Immunologie, Immunopathologie et Chimie Thérapeutique, CNRS UPR3572, Institut de Biologie Moléculaire et Cellulaire, Strasbourg, France.
Pauline Le Van QuyenService d'anatomopathologie, Hôpitaux universitaires de Strasbourg, Strasbourg, France.
Hélène DumortierLaboratoire d'Immunologie, Immunopathologie et Chimie Thérapeutique, CNRS UPR3572, Institut de Biologie Moléculaire et Cellulaire, Strasbourg, France.
Fanny MonneauxLaboratoire d'Immunologie, Immunopathologie et Chimie Thérapeutique, CNRS UPR3572, Institut de Biologie Moléculaire et Cellulaire, Strasbourg, France.
Jacques-Eric GottenbergService de rhumatologie, Centre National de Référence des Maladies Autoimmunes et Systémiques Rares, Hôpitaux universitaires de Strasbourg, Strasbourg, France renaud.felten@chru-strasbourg.fr jacques-eric.gottenberg@chru-strasbourg.fr.ORCID 0000-0002-9469-946X
Centre National de la Recherche Scientifique · FRHôpitaux Universitaires de Strasbourg · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveInnate lymphoid cells (ILCs) are a cell population implicated in the pathogenesis of various chronic inflammatory diseases, but little is known about their role in primary Sjögren's syndrome (pSS). The aim of this study was to assess the frequency of ILC subsets in peripheral blood (PB) and their quantity and location in minor salivary glands (MSGs) in pSS.

methodsThe frequency of ILC subsets was analysed in the PB of patients with pSS and healthy controls (HCs) by flow cytometry. The amount and location of ILC subsets in MSGs were studied in patients with pSS and sicca controls by immunofluorescence assay.

resultsIn PB, the frequency of ILC subsets did not differ between patients with pSS and HCs. The circulating frequency of the ILC1 subset was increased in patients with pSS with positive anti-SSA antibodies and that of the ILC3 subset was reduced in patients with pSS with glandular swelling. In MSGs, the ILC3 number was higher in lymphocytic-infiltrated than non-infiltrated tissue in patients with pSS and normal glandular tissues in sicca controls. The ILC3 subset was preferentially located at the periphery of infiltrates and was more abundant in small infiltrates of recently diagnosed pSS.

conclusionAltered ILC homeostasis mainly concerns salivary glands in pSS. Most ILCs in MSGs consist of the ILC3 subset, located at the periphery of lymphocytic infiltrates. The ILC3 subset is more abundant in smaller infiltrates and in recently diagnosed pSS. It might play a pathogenic role in the development of T and B lymphocyte infiltrates in the early stages of pSS.

Indexed as

Sjogren's SyndromeHumansImmunity, InnateLymphocytesSalivary GlandsSalivary Glands, MinorAutoimmunitySjogren's SyndromeT-Lymphocyte subsets

Identifiers

PMID37230761
PMCPMC10230975
OpenAlexW4378211259

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.