The Open Arthritis Journal

2010, 3 : 24-31
Published online 2010 January 12. DOI: 10.2174/1876539401003010024
Publisher ID: TOARTHJ-3-24

RESEARCH ARTICLE
Dendritic Cell Biology in Animal Models of Arthritis

Robert Benson, * , James Brewer , Paul Garside and Iain B. McInnes
Division of Immunology, Infection and Inflammation, University of Glasgow, Scotland, UK

* Address correspondence to this author at the Glasgow Biomedical Research Centre, Division of Immunology, Infection and Inflammation, Faculty of Medicine, University of Glasgow, 120 University Place, Glasgow G12 8QQ, Scotland, UK; Tel: 44 141 3308412; Fax: 44 141 337 3217; E-mail: benson@clinmed.gla.ac.uk

ABSTRACT

In recent years the treatment of rheumatoid arthritis (RA) has changed considerably with the advent of novel biologic agents that target cytokines such as TNF. The impact on clinical practice has been considerable with achievement of high hurdle endpoints and reduced articular damage. Unfortunately, remission that is long lasting is rarely achieved and almost never reached in the absence of chronic drug therapy. Thus, interest in what should be the critical objective of autoimmune therapeutics – the re-establishment of self-tolerance – has become increasingly prominent. Models of experimental arthritis have only just begun to reveal the intricacies of dendritic cell (DC) biology in RA. And while manipulation of antigen presenting cells such as DCs can be used in the suppression of experimental arthritis, the basic functions and mechanisms regarding their impact is mostly obtained indirectly by inference from other autoimmune and infectious studies. Indeed, our understanding of the contribution of DC biology to induction and perpetuation of RA is relatively ill defined. Here we discuss recent advances in understanding basic DC biology, their roles in, and impact on, experimental arthropathy and resulting therapeutic implications. It is essential that more research into the direct contribution of DC activity in RA is forthcoming, particularly as they could hold the key to development of antigen specific therapeutics. The major contributing factor to this knowledge deficit is the difficulty inherent in investigating what are most likely pre-clinical immunological events, an area more suited to study in animal models.

Keyword:

Dendritic cell, Arthritis, Animal model, Autoimmune, Tolerance.