Evidence map›Paper›PMID 41811880›Full record

ArticleJournal of immunology research2026

CD39 Expression in Peripheral CD4+ T Lymphocytes Is Associated With Disease Activity in Patients With Systemic Lupus Erythematosus.

Hao Jin, Lu Tang

Abstract read
In one paragraph

Article in Journal of immunology research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Hao JinTechnology Transfer Department, Tianjin Cancer Hospital Airport Hospital, Tianjin, China.ORCID https://orcid.org/0000-0002-4878-118X
Lu TangDivision of Rheumatology, Tianjin First Central Hospital, Tianjin, China, tj-fch.com.ORCID https://orcid.org/0000-0001-7517-5946

Funding

National Natural Science Foundation of China 81602020Tianjin Binhai New Area Health Research Project 2024BWKZ09
6 · The paper itself

Abstract

objectiveRegulatory T cells (Tregs) and CD4-positive T cells are crucial for the immunological control of systemic lupus erythematosus (SLE). As a crucial component of the adenosine metabolism pathway, CD39 influences the development and functionality of several immune system lymphocyte subsets, such as CD4-positive T cells and Tregs. The purpose of this study was to examine the connection between the activity of SLE disease and the numbers of Tregs and CD4-positive T lymphocytes, as well as the expression levels of the CD39 molecule on these cells.

methodsOne hundred and eight SLE patients had peripheral blood drawn. The patients were split into two distinct categories: the SLE active group and the SLE low-activity group, depending on the illness activity. Using flow cytometry, the proportions and absolute numbers of CD4-positive T cells and Tregs, as well as the expression of CD39 on these cells, were measured. Their associations with SLE disease activity were examined. Last, CD39 was assessed as a possible biomarker for the activity of SLE illness.

resultsCompared to the SLE low-activity group, the SLE active group's peripheral blood had a larger percentage and quantity of CD4-positive T cells. In contrast, it was discovered that the SLE active group had fewer Tregs overall, both in terms of percentage and quantity, than the SLE low-activity group. Compared to those in the SLE low-activity group, patients in the SLE active group exhibited noticeably greater levels of CD39 expression in both Tregs and CD4-positive T cells. Additionally, this study showed a favorable correlation between the percentage and absolute quantity of Tregs and the expression level of CD39 on Tregs. On the other hand, there is a negative correlation between the percentage and absolute quantity of CD4-positive T cells and the expression level of CD39 on these cells. Furthermore, CD39 is a possible biomarker that could help in the identification of SLE disease activity, according to receiver operating characteristic (ROC) curve research.

conclusionAccording to this study, CD4-positive T cells' surface CD39 molecule serves a similar purpose to Tregs', namely immunological suppression. Therefore, a subpopulation of T cells with immunosuppressive properties is defined by CD4+CD39+ T lymphocytes, which may be a more accurate marker for differentiating disease activity in SLE.

Indexed as

Antigens, CDApyraseCD4-Positive T-LymphocytesLupus Erythematosus, SystemicT-Lymphocytes, RegulatoryAdultBiomarkersFemaleFlow CytometryHumansImmunophenotypingLymphocyte CountMaleMiddle AgedSeverity of Illness IndexT-Lymphocyte SubsetsAntigens, CDApyraseBiomarkersCD39 antigenENTPD1 protein, humanCD39CD4-positive T lymphocytesdisease activitysystemic lupus erythematosusTregs

Identifiers

PMID41811880
PMCPMC13140799

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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.