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Role of tumour necrosis factor α in experimental arthritis: separate activity of interleukin 1β in chronicity and cartilage destruction
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  1. Wim B van den Berga,
  2. Leo A B Joostena,
  3. George Kolliasb,
  4. Fons A J van de Looa
  1. aDepartment of Rheumatology, University Hospital Nijmegen, the Netherlands, bDepartment of Molecular Genetics, Hellenic Pasteur Institute, Athens, Greece
  1. Professor W B van den Berg, Geert Grooteplein Zuid 8, 6500 HB Nijmegen, the Netherlands.

Abstract

Chronic arthritis is characterised by persistent joint inflammation and concomitant joint destruction. Using murine arthritis models and neutralising antibodies as well as cytokine specific knockout conditions, it was found that tumour necrosis factor α (TNFα) is important in early joint swelling. Membrane bound TNFα is sufficient to drive this aspect of inflammation as well as the acute cellular infiltrate in the synovial tissue. Interleukin 1 (IL1) is not necessarily a dominant cytokine in early joint swelling, but has a pivotal role in sustained cellular infiltration and erosive cartilage damage. TNFα independent IL1 production is a prominent feature in murine arthritis models. These observations provide evidence for potential uncoupling of joint inflammation and erosive changes, implying that both cytokines need to be targeted to achieve optimal treatment.

  • tumour necrosis factor α
  • rheumatoid arthritis
  • cartilage
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