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Updated: Sep 6, 2025

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Published on: June 6, 2025
Upregulated miR-146a Expression in Peripheral Blood Relates to Th17 and Treg Imbalance in Elder Rheumatoid Arthritis
Menglan Liu1, Tianli Ren2, Zhi Lin1
1Department of Geriatrics, Wuxi No. 2 People's Hospital Affiliated to Nanjing Medical University, Wuxi, China.
Background:
The expression level of microRNA-146a (miR-146a) increased in peripheral blood and synovialis tissue of rheumatoid arthritis (RA) patient, and it may play an important role in the pathological process of RA. We investigated its possibility as a diagnostic marker and the correlation with T helper 17 (Th17) and Treg cells in elder RA patients.
Methods:
Blood samples were collected from 38 active RA patients, 38 inactive RA patients, and 40 healthy controls. RNA expression levels of miR-146a were detected from the peripheral blood samples. The proportion of Th17 and Treg cells were analyzed, as well as their cell-specific transcription factor retinoic acid-related orphan receptor variant 2 (RORc) and forkhead box protein 3 (FOXP3). Furthermore, secretion of pre-inflammatory and anti-inflammatory factors was detected. Correlations between miR-146a and these factors were also analyzed.
Results:
Compared with healthy control, expression levels of miR-146a in inactive and active groups were significantly higher, with the highest level in active group. The expression of miR-146a and the RA severity, Th17 cell ratio, RORc expression, IL-17 level showed a significant positive correlation, while it showed a significantly negative correlation with Treg cell ration, FOXP3 expression, and TGF-β1 secretion.
Conclusions:
These results suggested that miR-146a may be used as a disease progression marker in the peripheral blood of elder RA patients.
Insights
MicroRNA-146a (miR-146a) levels are elevated in rheumatoid arthritis (RA) patients, correlating with disease severity and immune cell balance. This suggests miR-146a could serve as a diagnostic marker for RA progression in elderly individuals.
Area of Science:
- Immunology
- Molecular Biology
- Rheumatology
Background:
- Rheumatoid arthritis (RA) is characterized by increased microRNA-146a (miR-146a) expression in peripheral blood and synovial tissue.
- miR-146a is implicated in the pathological processes of RA, necessitating further investigation into its role.
- The study focuses on elderly RA patients, exploring miR-146a's potential as a diagnostic marker and its relationship with T helper 17 (Th17) and regulatory T (Treg) cells.
Purpose of the Study:
- To investigate the potential of miR-146a as a diagnostic marker in elderly rheumatoid arthritis patients.
- To analyze the correlation between miR-146a expression and the balance of Th17 and Treg cells in RA.
- To examine the relationship between miR-146a levels and disease severity, immune cell populations, and cytokine profiles in RA.
Main Methods:
- Blood samples were collected from 38 active RA patients, 38 inactive RA patients, and 40 healthy controls.
- RNA expression levels of miR-146a were quantified using peripheral blood samples.
- Proportions of Th17 and Treg cells, their transcription factors (RORc and FOXP3), and cytokine secretion (pro- and anti-inflammatory) were analyzed. Correlations with miR-146a were assessed.
Main Results:
- miR-146a expression was significantly higher in both inactive and active RA groups compared to healthy controls, with the highest levels in the active RA group.
- miR-146a expression positively correlated with RA severity, Th17 cell ratio, RORc expression, and IL-17 levels.
- Conversely, miR-146a expression negatively correlated with Treg cell ratio, FOXP3 expression, and TGF-β1 secretion.
Conclusions:
- miR-146a exhibits potential as a disease progression marker in the peripheral blood of elderly RA patients.
- The findings highlight miR-146a's association with immune dysregulation, specifically the Th17/Treg balance, in RA pathogenesis.
- miR-146a may serve as a valuable biomarker for monitoring RA activity and progression.
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