Best Practice & Research Clinical Rheumatology
Volume 24, Issue 4 , Pages 527-540, August 2010

Therapeutic opportunities in fibroblasts in inflammatory arthritis

  • Marianne Niedermeier

      Affiliations

    • Institute for Experimental Musculoskeletal Medicine, University Hospital Muenster, Domagkstrasse 3, D-48149 Münster, Germany
    • Internal Medicine D, Department of Nephrology and Rheumatology, University Hospital Muenster, Domagkstrasse 3, D-48149 Münster, Germany
    • Tel.: +49 251 835 7799; Fax: +49 251 835 7462.
  • ,
  • Thomas Pap

      Affiliations

    • Institute for Experimental Musculoskeletal Medicine, University Hospital Muenster, Domagkstrasse 3, D-48149 Münster, Germany
    • Corresponding Author InformationCorresponding author. Tel.: +49 251 835 7799; Fax: +49 251 835 7462.
  • ,
  • Adelheid Korb

      Affiliations

    • Internal Medicine D, Department of Nephrology and Rheumatology, University Hospital Muenster, Domagkstrasse 3, D-48149 Münster, Germany
    • Tel.: +49 251 835 7799; Fax: +49 251 835 7462.

The Identification of key players of inflammation and pathologic immune response in rheumatoid arthritis (RA) has resulted in the development of novel therapeutic strategies revolutionising the treatment of disease. However, these new therapeutics only indirectly affect the mesenchymal compartment of the inflamed synovium and, in particular, the specific phenotype of activated fibroblast-like cells. These cells have been demonstrated to trigger not only the progressive destruction of articular cartilage and bone but also the switch from acute to chronic inflammation. Therefore, targeting of this population of fibroblast-like cells may provide interesting opportunities to go beyond the mere inhibition of inflammation and to interfere with key disease processes in RA. This review summarises our current knowledge on the role of fibroblast-like cells in RA and points to potentials ways of modulating their disease-specific activation.

Keywords: fibroblast-like synoviocytes, rheumatoid arthritis, extracellular matrix degradation, stable activation, apoptosis, matrix metalloproteinases, adhesion molecules

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S1521-6942(10)00026-4

doi:10.1016/j.berh.2010.02.002

Best Practice & Research Clinical Rheumatology
Volume 24, Issue 4 , Pages 527-540, August 2010