Detection of circulating Fc epsilon R2/CD23+ monocytes in patients with rheumatic diseases

H Becker1, P Potyka, C Weber

  • 1Third Medicine Clinic and Poliklinik, Justus-Liebig University Giessen, Germany.

Insights

Interleukin-4 (IL-4) induces Fc epsilon R2/CD23 on monocytes. Elevated Fc epsilon R2/CD23+ monocytes are found in progressive systemic sclerosis (PSS) and other rheumatic diseases, suggesting IL-4

Area of Science:

  • Immunology
  • Rheumatology
  • Cell Biology

Background:

  • Interleukin-4 (IL-4) is known to induce Fc epsilon R2/CD23 expression on monocytes in vitro.
  • The role of IL-4 and monocyte interactions in rheumatic diseases requires further investigation.

Purpose of the Study:

  • To investigate the interaction of IL-4 and monocytes in patients with rheumatic diseases.
  • To determine the frequency of Fc epsilon R2/CD23+ monocytes in various rheumatic conditions.

Main Methods:

  • Flow cytometry was employed to quantify Fc epsilon R2/CD23+ monocytes.
  • Analysis included patients with progressive systemic sclerosis (PSS), rheumatoid arthritis, and systemic lupus erythematosus.
  • Monocyte-activating capacity of supernatants from PSS patient cells was assessed.

Main Results:

  • Elevated numbers of circulating Fc epsilon R2/CD23+ monocytes were observed in PSS patients compared to controls.
  • Supernatants from PSS patients' peripheral blood mononuclear cells showed enhanced ability to induce Fc epsilon R2/CD23 on CD14+ monocytes.
  • Increased Fc epsilon R2/CD23+ monocyte frequency was also noted in rheumatoid arthritis and systemic lupus erythematosus, correlating with disease activity.

Conclusions:

  • IL-4 plays a significant role in the pathogenesis of PSS through monocyte activation.
  • IL-4 may also contribute to monocyte activation in other rheumatic diseases.
  • Fc epsilon R2/CD23+ monocytes serve as potential biomarkers for disease activity in rheumatic conditions.

Related Concept Videos