Systemic Administration of Tolerogenic Dendritic Cells Ameliorates Murine Inflammatory Arthritis

Louise J Healy, Helen L Collins, Stephen J Thompson*
Division of Immunology, Infection and Inflammatory Diseases, King’s College London, London, UK

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© Healy et al.; Licensee Bentham Open

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* Address correspondence to this author at the Department of Rheumatology,Kings College London, Hodgkin Building 3.60 W, Guys Campus, London SE1 1UL, UK; Tel: 0207 8486041; E-mail:


The expression of various cell surface molecules and the production of certain cytokines are important mechanisms by which dendritic cells (DC) are able to bias immune responses. This paper describes the effects of the inflammatory cytokine tumor necrosis factor (TNF)-αon DC phenotype and function. TNF-αtreatment resulted in upregulation of MHC class II and CD86 in the absence of increased cell surface CD40 and CD80 or the production of IL-12. Additionally TNF-αtreated cells were able to bias T cell responses towards an anti-inflammatory profile. On a note of caution this tolerogenic phenotype of the DC was not stable upon subsequent TLR-4 ligation as a 4 hour pulse of the TNF-α treated DC with lipopolysaccharide (LPS) resulted in the restoration of IL-12 production and an enhancement of their T cell stimulatory capacity which resulted in an increased IFN-γproduction. However, TNF-αtreated DC, when administered in vivo, were shown to ameliorate disease in collagen induced arthritis, an experimental model of inflammatory joint disease. Mice receiving TNF-αtreated DC but not LPS matured DC had a delayed onset, and significantly reduced severity, of arthritis. Disease suppression was associated with reduced levels of collagen specific IgG2a and decreased inflammatory cell infiltration into affected joints. In summary the treatment of DC with TNF-αgenerates an antigen presenting cell with a phenotype that can reduce the pro-inflammatory response and direct the immune system towards a disease modifying, anti-inflammatory state.