Evidence map›Paper›PMID 35526080›Full record

ArticleArthritis research & therapy2022

Impaired activation of STAT5 upon IL-2 stimulation in Tregs and elevated sIL-2R in Sjögren's syndrome.

Magdalena Keindl, Richard Davies, Brith Bergum, Johan G Brun, Daniel Hammenfors, Roland Jonsson, Valeriya Lyssenko, Silke Appel

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Article in Arthritis research & therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

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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

16 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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.

Magdalena KeindlBroegelmann Research Laboratory, Department of Clinical Science, University of Bergen, 5020, Bergen, Norway. magdalena.keindl@uib.no.ORCID 0000-0002-7163-0179
Richard DaviesBroegelmann Research Laboratory, Department of Clinical Science, University of Bergen, 5020, Bergen, Norway.
Brith BergumFlow Cytometry Core Facility, Department of Clinical Science, Faculty of Medicine, University of Bergen, Bergen, Norway.
Johan G BrunDepartment of Rheumatology, Haukeland University Hospital, Bergen, Norway.
Daniel HammenforsDepartment of Rheumatology, Haukeland University Hospital, Bergen, Norway.
Roland JonssonBroegelmann Research Laboratory, Department of Clinical Science, University of Bergen, 5020, Bergen, Norway.
Valeriya LyssenkoCenter for Diabetes Research, Department of Clinical Science, University of Bergen, Bergen, Norway.
Silke AppelBroegelmann Research Laboratory, Department of Clinical Science, University of Bergen, 5020, Bergen, Norway. silke.appel@uib.no.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInterleukin-2 (IL-2) and the high-affinity IL-2 receptor (IL-2R) are essential for the survival of regulatory T cells (Tregs) which are the main players in immune tolerance and prevention of autoimmune diseases. Sjögren's syndrome (SS) is a chronic autoimmune disease predominantly affecting women and is characterised by sicca symptoms including oral and ocular dryness. The aim of this study was to investigate an association between IL-2R and Treg function in patients with SS of different severity defined by the salivary flow rate.

methodsIn a cross-sectional study, we determined plasma soluble IL-2R (sIL-2R) levels in women with SS (n=97) and healthy females (n=50) using ELISA. A subset of those (n=51) was screened for Treg function measured by the STAT5 signalling response to IL-2 using phospho-flow cytometry.

resultsWe found that elevated plasma levels of sIL-2R were positively associated with the severity of SS reflected by a pathologically low salivary flow. Phospho-flow analysis revealed that patients with SS have a significantly lower frequency of pSTAT5

conclusionsOur data indicates that Tregs have a weakened immunosuppressive function in patients with SS due to impaired IL-2/IL-2R signalling capacity. This could mediate lymphocytic infiltration into salivary glands inducing sicca symptoms. We believe that sIL-2R could act as a useful indicator for SS and disease severity.

Indexed as

Interleukin-2Sjogren's SyndromeSTAT5 Transcription FactorCross-Sectional StudiesFemaleHumansReceptors, Interleukin-2T-Lymphocytes, RegulatoryTumor Suppressor ProteinsInterleukin-2Receptors, Interleukin-2STAT5A protein, humanSTAT5 Transcription FactorTumor Suppressor ProteinsCD25IL2RAImmune tolerancePhospho-flow cytometryRegulatory T cells

Identifiers

PMID35526080
PMCPMC9077945

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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.