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CD39 Expression in Peripheral CD4+ T Lymphocytes Is Associated With Disease Activity in Patients With Systemic Lupus
1Technology Transfer Department, Tianjin Cancer Hospital Airport Hospital, Tianjin, China.
Journal of Immunology Research
|March 11, 2026
Summary
Systemic lupus erythematosus (SLE) disease activity correlates with CD4-positive T cells and regulatory T cells (Tregs). CD39 expression on these cells, particularly CD4+CD39+ T lymphocytes, may serve as a biomarker for SLE activity.
Area of Science:
- Immunology
- Molecular Biology
- Rheumatology
Background:
- Regulatory T cells (Tregs) and CD4-positive T cells are vital for controlling Systemic Lupus Erythematosus (SLE).
- CD39, a key enzyme in adenosine metabolism, impacts lymphocyte subsets, including CD4+ T cells and Tregs.
Purpose of the Study:
- To investigate the relationship between SLE disease activity and the counts of Tregs and CD4-positive T lymphocytes.
- To analyze the expression levels of CD39 on these immune cells in SLE patients.
- To evaluate CD39 as a potential biomarker for SLE disease activity.
Main Methods:
- Peripheral blood samples from 108 SLE patients were analyzed using flow cytometry.
- Patients were categorized into active and low-activity SLE groups.
- Quantified proportions and absolute numbers of CD4+ T cells and Tregs, along with CD39 expression, and correlated these with disease activity.
Main Results:
- Active SLE patients showed higher CD4+ T cell counts but lower Treg numbers compared to the low-activity group.
- Increased CD39 expression was observed on both Tregs and CD4+ T cells in active SLE patients.
- CD39 expression on Tregs positively correlated with Treg numbers, while on CD4+ T cells, it negatively correlated.
Conclusions:
- CD39 on CD4-positive T cells appears to mediate immunosuppression, similar to Tregs.
- The CD4+CD39+ T lymphocyte subset may represent a more precise marker for distinguishing SLE disease activity.
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