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Mice transgenic for BAFF develop lymphocytic disorders along with autoimmune manifestations
F Mackay1, S A Woodcock, P Lawton
1Department of Immunology, Inflammation and Cell Biology, Biogen, Cambridge, Massachusetts 02142, USA. fabienne_mackay@biogen.com
Abstract:
The cause of many autoimmune and inflammatory diseases is unresolved, although dysregulated production of tumor necrosis factor (TNF) family members appears to be important in many cases. BAFF, a new member of the TNF family, binds to B cells and costimulates their growth in vitro. Mice transgenic for BAFF have vastly increased numbers of mature B and effector T cells, and develop autoimmune-like manifestations such as the presence of high levels of rheumatoid factors, circulating immune complexes, anti-DNA autoantibodies, and immunoglobulin deposition in the kidneys. This phenotype is reminiscent of certain human autoimmune disorders and suggests that dysregulation of BAFF expression may be a critical element in the chain of events leading to autoimmunity.