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Charlotte Thompson1,2, Ruth Davies1, Anwen Williams1
1CREATE Centre, Section of Rheumatology, Division of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom.
CD8+CD28- T cells are elevated in Rheumatoid Arthritis (RA) patients and correlate with disease duration. Cytomegalovirus (CMV) seropositivity is associated with higher levels of these cells in early RA.
Area of Science:
- Immunology
- Rheumatology
- Cell Biology
Background:
- CD3+CD8+CD28- T cells, a subset of cytotoxic T lymphocytes, are implicated in autoimmune diseases.
- Elevated levels of CD3+CD8+CD28- T cells have been observed in Rheumatoid Arthritis (RA).
Purpose of the Study:
- To investigate the prevalence of CD3+CD8+CD28- T cells in early RA.
- To determine the association between CD3+CD8+CD28- T cells, disease duration, and cytomegalovirus (CMV) seropositivity in RA patients.
Main Methods:
- Prospective observational study involving 50 RA patients (25 early, 25 established) and 25 healthy controls.
- Flow cytometry analysis of peripheral blood mononuclear cells to quantify CD3+CD8+CD28- T cells.
- Assessment of clinical and serological markers, including CMV serostatus and C-reactive protein (CRP).
Main Results:
- CD3+CD8+CD28- T cells were significantly increased in RA patients compared to controls.
- The percentage of CD3+CD8+CD28- T cells correlated positively with disease duration in RA.
- Elevated CD3+CD8+CD28- T cells were observed in CMV-seropositive RA patients, particularly in the early disease stage.
Conclusions:
- Increased CD3+CD8+CD28- T cells are a feature of RA, potentially playing a role early in disease pathogenesis.
- CMV seropositivity may contribute to the expansion of CD3+CD8+CD28- T cells in RA, suggesting a potential role for CMV in RA development.
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