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Increased TTS expression in patients with rheumatoid arthritis
Jiaxi Chen1, Li Jun, Chen Shiyong
1Department of Clinical Laboratory, Taizhou Hospital of Zhejiang Province, Affiliated Hospital of Wenzhou Medical College, Taizhou, Zhejiang Province, China.
Clinical and Experimental Medicine
|February 12, 2014
Summary
Tryptophanyl-tRNA synthetase (TTS) expression is elevated in rheumatoid arthritis (RA) patients, particularly in T cells. This finding may offer insights into RA pathogenesis and disease progression.
Area of Science:
- Immunology
- Molecular Biology
- Rheumatology
Background:
- Immune system activation plays a role in rheumatoid arthritis (RA) pathogenesis.
- Imbalances in specific enzymes like indoleamine 2,3-dioxygenase (IDO) and tryptophanyl-tRNA synthetase (TTS) are implicated in autoimmune diseases.
Purpose of the Study:
- To investigate the differential expression of IDO and TTS in patients with RA compared to healthy controls.
- To explore the correlation between TTS expression and disease activity markers in RA.
Main Methods:
- Real-time quantitative polymerase chain reaction (RT-qPCR) to measure mRNA expression levels.
- Flow cytometry to analyze protein expression on peripheral blood mononuclear cells (PBMCs), specifically within CD3(+) T cells.
- Analysis of 49 RA patients and 49 healthy controls.
Main Results:
- TTS mRNA expression was significantly higher in RA patients than in healthy controls.
- Elevated TTS expression correlated with erythrocyte sedimentation rate (ESR), a marker of inflammation (r = 0.424, P < 0.01).
- Increased TTS expression was predominantly observed in CD3(+) T cells within the RA cohort.
Conclusions:
- The study identifies an upregulation of TTS in RA patients, suggesting its involvement in the disease.
- Increased TTS in T cells may contribute to the survival of autoreactive T cells, a key factor in RA.
- Measuring TTS expression could enhance understanding of RA progression and potentially identify therapeutic targets.
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