Granulocyte and monocyte apheresis suppresses symptoms of rheumatoid arthritis: a pilot study

Rheumatol Int. 1998;18(3):113-8. doi: 10.1007/s002960050068.

Abstract

To investigate if granulocyte and monocyte apheresis mitigates the symptoms of rheumatoid arthritis (RA), and influences production of panmyelocytes (CD15+ CD16- cells) at the bone marrow level, 27 RA patients who had elevated granulocyte counts were recruited. The granulocyte and monocyte apheresis column (G-1 column) is an extracorporeal type device packed with 220 g cellulose acetate beads to which granulocytes and monocytes specifically adhere. Patients received apheresis of 1 hr duration twice per week, 8 times over a period of 4 weeks. To prepare CD15+CD16- cells, iliac bone marrow aspirate was obtained at baseline and at 2 weeks after completion of the apheresis course. Ex-vivo proliferation of bone marrow low density cells and production of IgM-RF were also investigated. Following granulocyte and monocyte apheresis, there was a suppressed tendency in the number of CD15+CD16- cells in patients with high bone marrow CD15+CD16- cell counts at baseline. Clinical assessments 2 weeks after the completion of apheresis therapy showed improvements in swollen joint count (P < 0.001), tender joint count (P < 0.001) and duration of morning stiffness (P < 0.005). The results suggest that granulocytes and monocytes/macrophages have a pathological role in RA and apheresis treatment to reduce or suppress these cells should benefit patients with RA.

Publication types

  • Clinical Trial

MeSH terms

  • Adult
  • Aged
  • Arthritis, Rheumatoid / metabolism
  • Arthritis, Rheumatoid / therapy*
  • Blood Transfusion, Autologous
  • Cytokines / metabolism
  • Female
  • Flow Cytometry
  • Granulocytes
  • Humans
  • Leukapheresis*
  • Leukocyte Count
  • Leukocyte Transfusion*
  • Lewis X Antigen / metabolism
  • Male
  • Middle Aged
  • Monocytes
  • Pilot Projects
  • Receptors, IgG / metabolism
  • Rheumatoid Factor / metabolism
  • Treatment Outcome

Substances

  • Cytokines
  • Lewis X Antigen
  • Receptors, IgG
  • Rheumatoid Factor