Abstract
B cells play a key role in regulating the immune system by producing antibodies, acting as antigen-presenting cells, providing support to other mononuclear cells, and contributing directly to inflammatory pathways. Accumulating evidence indicates that there is a disruption of these regulated processes in the pathogenesis of autoimmune diseases, including rheumatoid arthritis (RA). In RA there is a chronic inflammation in the affected joints leading to the development of ectopic germinal centers. A micro-environment is established which supports B cell activation and differentiation. Plasma cells may develop which secrete autoantibodies of high affinity directly into the synovial tissue. As a result, antigen/antibody complex formation, the activation of the complement cascade and the stimulation of macrophages may contribute to the destruction of joints. B cells also play a pivotal role in the activation of synovial T cells and the induction of cytokine secretion. Finally, the success of B cell depletion therapy by using monoclonal antibodies against CD20 further emphasized the importance of B cells in the pathogenesis of RA (English) [ABSTRACT FROM AUTHOR]
Original language | English (US) |
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Pages (from-to) | 34-44 |
Number of pages | 11 |
Journal | MedUNAB |
Volume | 9 |
Issue number | 1 |
State | Published - Apr 2006 |