CD28- Cells Are Increased in Early Rheumatoid Arthritis and Are Linked With Cytomegalovirus Status

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.

Insights

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.