Deficient Fas ligand expression by synovial lymphocytes from patients with rheumatoid arthritis

Arthritis Rheum. 1997 Sep;40(9):1644-52. doi: 10.1002/art.1780400914.

Abstract

Objective: To examine the expression and function of CD95 (Fas) and its ligand in rheumatoid arthritis (RA).

Methods: We used flow cytometry and reverse transcriptase-polymerase chain reaction methods to assess lymphocyte expression of CD95 and its ligand. We also examined whether lymphocytes could undergo Fas-mediated apoptosis with anti-CD95 monoclonal antibody (MAb) or human Fas ligand-expressing fibroblasts, and if synovial fluid contained a soluble factor(s) that could inhibit such interactions. Finally, we determined whether anti-CD3 MAb could induce synovial T cells to express the Fas ligand in vitro.

Results: Nearly all RA synovial fluid or synovial tissue lymphocytes expressed CD95 and could be induced to undergo apoptosis by CD95 crosslinking. We did not detect a soluble inhibitor in RA synovial fluid that could account for the survival of CD95+ synovial cells in vivo. Instead, we detected little or no expression of Fas ligand by RA synovial lymphocytes. However, we could induce such cells to express Fas ligand with anti-CD3 MAb or phorbol ester and ionomycin in vitro.

Conclusion: There is ineffective clearance of activated cells in the RA joint due to deficient expression of the Fas ligand.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Apoptosis
  • Arthritis, Rheumatoid / metabolism*
  • B-Lymphocytes / metabolism*
  • DNA Primers / chemistry
  • Flow Cytometry
  • Humans
  • Leukocyte Count
  • Ligands
  • Polymerase Chain Reaction
  • Synovial Fluid / cytology*
  • Synovial Fluid / metabolism
  • Synovial Membrane / cytology*
  • Synovial Membrane / metabolism
  • T-Lymphocytes / metabolism*
  • fas Receptor / biosynthesis*
  • fas Receptor / immunology

Substances

  • DNA Primers
  • Ligands
  • fas Receptor