Evidence map›Paper›PMID 29565987›Full record

ArticlePloS one2018

PhosphoLipid transfer protein (PLTP) exerts a direct pro-inflammatory effect on rheumatoid arthritis (RA) fibroblasts-like-synoviocytes (FLS) independently of its lipid transfer activity.

Rachel Audo, Valérie Deckert, Claire I Daien, Hélène Che, Jamila Elhmioui, Stéphanie Lemaire, Jean-Paul Pais de Barros, Catherine Desrumaux, Bernard Combe, Michael Hahne and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
6.9field-weighted citation impact, top 3% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

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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

12 authors at 3 institutions in 1 country.

Rachel AudoDepartment of Rheumatology, Montpellier University and Lapeyronie Teaching Hospital, Montpellier, France.ORCID 0000-0002-0021-5349
Valérie DeckertLNC Lipids, Nutrition and Cancer, INSERM UMR1231, Dijon, France.
Claire I DaienDepartment of Rheumatology, Montpellier University and Lapeyronie Teaching Hospital, Montpellier, France.
Hélène CheDepartment of Rheumatology, Montpellier University and Lapeyronie Teaching Hospital, Montpellier, France.
Jamila ElhmiouiMontpellier University, Montpellier, France.
Stéphanie LemaireLNC Lipids, Nutrition and Cancer, INSERM UMR1231, Dijon, France.
Jean-Paul Pais de BarrosLNC Lipids, Nutrition and Cancer, INSERM UMR1231, Dijon, France.
Catherine DesrumauxLipSTIC LabEx, Fondation de Coopération Scientifique Bourgogne-Franche Comté, Dijon, France.
Bernard CombeDepartment of Rheumatology, Montpellier University and Lapeyronie Teaching Hospital, Montpellier, France.
Michael HahneMontpellier University, Montpellier, France.
Laurent LagrostLNC Lipids, Nutrition and Cancer, INSERM UMR1231, Dijon, France.
Jacques MorelDepartment of Rheumatology, Montpellier University and Lapeyronie Teaching Hospital, Montpellier, France.
Centre National de la Recherche Scientifique · FRInserm · FRUniversité de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is a chronic inflammatory rheumatic disease with modification of lipids profile and an increased risk of cardiovascular events related to inflammation. Plasma phospholipid transfer protein (PLTP) exerts a lipid transfer activity through its active form. PLTP can also bind to receptors such as ATP-binding cassette transporter A1 (ABCA1). In addition to its role in lipoprotein metabolism and atherosclerosis, the latest advances came in support of a complex role of PLTP in the regulation of the inflammatory response, both with pro-inflammatory or anti-inflammatory properties. The aim of the present study was to decipher the role of PLTP in joint inflammation and to assess its relevance in the context of RA. PLTP expression was examined by western-blot and by immunochemistry. ABCA1 expression was analyzed by flow cytometry. Lipid transfer activity of PLTP and pro-inflammatory cytokines were measured in sera and synovial fluid (SF) from RA patients and controls (healthy subjects or osteoarthritis patients [OA]). FLS were treated with both lipid-transfer active form and inactive form of recombinant human PLTP. IL-8, IL-6, VEGF and MMP3 produced by FLS were assessed by ELISA, and proliferation by measuring 3H-Thymidine incorporation. RA synovial tissues showed higher PLTP staining than OA and PLTP protein levels were also significantly higher in RA-FLS. In addition, RA, unlike OA patients, displayed elevated levels of PLTP activity in SF, which correlated with pro-inflammatory cytokines. Both lipid-transfer active and inactive forms of PLTP significantly increased the production of cytokines and proliferation of FLS. ABCA1 was expressed on RAFLS and PLTP activated STAT3 pathway. To conclude, PLTP is highly expressed in the joints of RA patients and may directly trigger inflammation and FLS proliferation, independently of its lipid transfer activity. These results suggest a pro-inflammatory role for PLTP in RA.

Indexed as

Arthritis, RheumatoidATP Binding Cassette Transporter 1Cell ProliferationCells, CulturedCytokinesFemaleFibroblastsGene ExpressionHumansInflammationLipid MetabolismMaleMiddle AgedOsteoarthritisPhospholipid Transfer ProteinsRecombinant ProteinsABCA1 protein, humanATP Binding Cassette Transporter 1CytokinesPhospholipid Transfer ProteinsRecombinant ProteinsSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID29565987
PMCPMC5863966
OpenAlexW2791866909

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.