Evidence map›Paper›PMID 38813034›Full record

ArticleTurkish journal of medical sciences2023

CD39 expression on immune cells predicts methotrexate response in rheumatoid arthritis patients.

Barış Boral, İbrahim Tuncer, Filiz Kibar, Salih Çetiner, Suade Özlem Badak, Emrah Salman, Emrah Koç, Eren Erken, Akgün Yaman

Abstract read
In one paragraph

Article in Turkish journal of medical sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

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

1 citing paper in PubMed.

  1. Article
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

9 authors.

Barış BoralDepartment of Immunology, Adana Health Practice and Research Center, University of Health Sciences, Adana, Turkiye.ORCID https://orcid.org/0000-0003-2175-8163
İbrahim TuncerDepartment of Immunology, Prof. Dr. Cemil Taşcıoğlu City Hospital, University of Health Sciences, İstanbul, Turkiye.ORCID https://orcid.org/0000-0002-6188-5266
Filiz KibarDepartment of Medical Microbiology, Faculty of Medicine, Çukurova University, Adana, Turkiye.ORCID https://orcid.org/0000-0003-2983-2399
Salih ÇetinerDepartment of Immunology, Faculty of Medicine, Çukurova University, Adana, Turkiye.ORCID https://orcid.org/0000-0002-5464-0340
Suade Özlem BadakDivision of Rheumatology, Department of Internal Medicine, Adana City Training and Research Hospital, Adana Turkiye.ORCID https://orcid.org/0000-0002-4661-787X
Emrah SalmanDepartment of Immunology, Ankara City Hospital, University of Health Sciences, Ankara, Turkiye.ORCID https://orcid.org/0000-0002-5293-0803
Emrah KoçDivision of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Çukurova University, Adana, Turkiye.ORCID https://orcid.org/0000-0002-7889-3051
Eren ErkenDivision of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Çukurova University, Adana, Turkiye.ORCID https://orcid.org/0000-0001-6902-624X
Akgün YamanDepartment of Immunology, Adana Health Practice and Research Center, University of Health Sciences, Adana, Turkiye.ORCID https://orcid.org/0000-0003-3309-3074

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/aim: Rheumatoid arthritis (RA) is a chronic inflammatory disease affecting mostly small joints, such as hand and foot joints symmetrically with irreversible joint destruction. In this study, the relationship between CD39 expression and the treatment response of RA patients was examined to investigate its potential as a biomarker that demonstrates treatment response. Materials and methods: This study included 77 RA patients and 40 healthy controls (HC). The RA patients were divided into 2 groups based on their response to RA treatment, those with a good response to methotrexate (MTX) monotherapy and those with an inadequate response based on the American College of Rheumatology and the European League Against Rheumatism response criteria. Various immunological parameters and Disease Activity Score in 28 Joints (DAS28) were examined between the groups using the Student's t-test. Results: The monocytic myeloid-derived suppressor cell (M-MDSC) percentage was higher in the RA patient group versus the HC group. The CD39 expression in the T lymphocytes were higher in patients that responded well to the MTX compared to those showing inadequate response. Additionally, s negative correlation was found between the DAS28 and CD39 in the T cells. Conclusion: The results showed that the improvement in treatment response to the therapy in RA patients could be because of the enhancement in the CD39/adenosine (ADO) pathway. Therefore, therapies targeting the CD39/ADO pathway in T cells may improve RA treatments.

Indexed as

Antirheumatic AgentsApyraseArthritis, RheumatoidMethotrexateAdultAgedAntigens, CDBiomarkersCase-Control StudiesFemaleHumansMaleMiddle AgedT-LymphocytesTreatment OutcomeAntigens, CDAntirheumatic AgentsApyraseBiomarkersCD39 antigenENTPD1 protein, humanMethotrexateadenosine pathwayCD39individualized treatmentmethotrexateRheumatoid arthritistreatment response

Identifiers

PMID38813034
PMCPMC10763742

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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.