Evidence map›Paper›PMID 27629388›Full record

ArticleArthritis research & therapy2016

Changes in peripheral blood lymphocyte subsets during arthritis development in arthralgia patients.

Joyce Lübbers, Marian H van Beers-Tas, Saskia Vosslamber, Samina A Turk, Sander de Ridder, Elise Mantel, John G Wesseling, Martine Reijm, Ingrid M van Hoogstraten, Johannes W Bijlsma and 3 more

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.6field-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

26 citing papers in PubMed, 52 citations in OpenAlex.

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  19. Rheumatoid arthritis CD14Clinical & translational immunology · 2021
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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

13 authors at 4 institutions in 1 country.

Joyce LübbersDepartment of Pathology, VU University Medical Center, Amsterdam, The Netherlands. j.lubbers@vumc.nl.ORCID 0000-0001-9265-5108
Marian H van Beers-TasAmsterdam Rheumatology and Immunology Center, Jan van Breemen Research Institute | Reade, Amsterdam, The Netherlands.
Saskia VosslamberDepartment of Pathology, VU University Medical Center, Amsterdam, The Netherlands.
Samina A TurkAmsterdam Rheumatology and Immunology Center, Jan van Breemen Research Institute | Reade, Amsterdam, The Netherlands.
Sander de RidderDepartment of Pathology, VU University Medical Center, Amsterdam, The Netherlands.
Elise MantelDepartment of Pathology, VU University Medical Center, Amsterdam, The Netherlands.
John G WesselingDepartment of Pathology, VU University Medical Center, Amsterdam, The Netherlands.
Martine ReijmDepartment of Pathology, VU University Medical Center, Amsterdam, The Netherlands.
Ingrid M van HoogstratenDepartment of Pathology, VU University Medical Center, Amsterdam, The Netherlands.
Johannes W BijlsmaAmsterdam Rheumatology and Immunology Center, VU University Medical Center, Amsterdam, The Netherlands.
Dirkjan van SchaardenburgAmsterdam Rheumatology and Immunology Center, Jan van Breemen Research Institute | Reade, Amsterdam, The Netherlands.
Hetty J BontkesDepartment of Pathology, VU University Medical Center, Amsterdam, The Netherlands.
Cornelis L VerweijDepartment of Pathology, VU University Medical Center, Amsterdam, The Netherlands.
Amsterdam UMC Location Vrije Universiteit Amsterdam · NLReade · NLAcademic Center for Dentistry Amsterdam · NLAmsterdam UMC Location University of Amsterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMultiple lymphocyte subsets like T and B cells have been connected to joint infiltration and inflammation in rheumatoid arthritis (RA). Identification of leucocyte subsets that are dysregulated in arthritis development could provide insight into the aetiology of RA. This study aimed to investigate the composition of the peripheral blood components, i.e. CD14(+) monocytes, CD4(+) and CD8(+) T lymphocytes (CD3(+)), CD80(+), C-X-C chemokine receptor 3 (CXCR3)(+) and CD27(+) B lymphocytes (CD19(+)), CD16(+)CD56(+)CD3(-) natural killer (NK) cells and activated CD56(+)CD3(+) T cells, for association with arthritis development in patients with arthralgia.

methodsPeripheral blood was collected from 89 patients with early RA (disease duration <6 months), 37 healthy controls (HC) and 113 patients with arthralgia (22 developed arthritis within ≤1 year, 18 developed arthritis after >1 year and 73 did not develop arthritis). Absolute numbers of monocytes and lymphocyte subsets in whole heparinized blood were determined with flow cytometry using quantification beads in combination with fluorescent labelled antibodies for T cells, B cells, monocytes, NK cells and activated T cells.

resultsIn patients with early RA, significant decreases in numbers of (activated) T cells, CD80(+) and memory B cells and a trend towards smaller numbers of CD8(+) T cells was observed compared to HC. Similar differences were seen in patients with arthralgia who developed or did not develop arthritis (non-converters), with significantly decreased CD8(+) T cells and memory B cells. Patients with arthralgia who developed arthritis were split into groups that developed arthritis within 1 year (early converters) or after 1 year (late converters). Late converters had a significantly decreased number of CD8(+) T cells compared to non-converters; early converters had a decreased number of memory B cells. Longitudinal analysis of converters showed a significant relative increase in CD80(+) B cells towards the conversion time point compared to 24 months prior to conversion.

conclusionsThis study revealed that patients with arthralgia who develop arthritis demonstrate a change in cellular immune parameters apparent in the periphery, starting with a decrease in cytotoxic T cells 24 months prior to arthritis development, followed by a decrease in the number of memory B cells 12 months prior to disease onset.

Indexed as

AdultAgedArthralgiaArthritis, RheumatoidFemaleFlow CytometryHumansLymphocyte SubsetsMaleMiddle AgedArthralgiaCell subsetsFlow cytometryRheumatoid arthritis

Identifiers

PMID27629388
PMCPMC5024500
OpenAlexW2519423795

What OpenQuestion holds

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LicenceCC BY
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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.