Anaemia of chronic disease in rheumatoid arthritis: in vivo effects of tumour necrosis factor alpha blockade

Br J Rheumatol. 1997 Sep;36(9):950-6. doi: 10.1093/rheumatology/36.9.950.

Abstract

Anaemia of chronic disease (ACD) is a common feature of active rheumatoid arthritis (RA). Inflammatory cytokines, particularly tumour necrosis factor alpha (TNF-alpha), interleukin-1 (IL-1) and interleukin-6 (IL-6), are thought to contribute to the pathogenesis of ACD, possibly by inhibiting erythropoietin (EPO) production. In this study, we examined the in vivo effects of TNF-alpha blockade with a chimeric monoclonal antibody, cA2, on erythropoiesis in RA patients with ACD. Administration of cA2 led to a dose-dependent increase in haemoglobin levels compared to placebo and these changes were accompanied by a reduction in both EPO and IL-6 levels. The data support the notion that TNF-alpha is important in the causation of ACD, but suggest a mechanism independent of EPO suppression. Instead, TNF-alpha may act directly on bone marrow red cell precursors.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anemia / etiology*
  • Anemia / therapy*
  • Antibodies, Monoclonal / pharmacology*
  • Arthritis, Rheumatoid / complications*
  • Arthritis, Rheumatoid / immunology
  • C-Reactive Protein / metabolism
  • Chronic Disease
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Erythropoietin / blood
  • Female
  • Hemoglobins / metabolism
  • Humans
  • Interleukin-6 / blood
  • Male
  • Recombinant Fusion Proteins / pharmacology
  • Tumor Necrosis Factor-alpha / immunology*

Substances

  • Antibodies, Monoclonal
  • Hemoglobins
  • Interleukin-6
  • Recombinant Fusion Proteins
  • Tumor Necrosis Factor-alpha
  • Erythropoietin
  • C-Reactive Protein