Increased levels of B lymphocyte stimulator (BLyS) are associated with syst
emic autoimmunity in animal models of spontaneous autoimmune disease, and t
ransgenic animals expressing BLyS develop typical autoimmune disease. Here,
we demonstrate significant elevations of BLyS in the patients with systemi
c lupus erythematosus (SLE). The BLyS isolated from the sera of SLE patient
s had the same m.w. as the natural soluble form and was able to stimulate B
cell activation in vitro. Increased BLyS in SLE patients was partially ass
ociated with higher levels of anti-dsDNA Ab of the IgG, IgM, and IgA classe
s, but not associated with the disease activity. Our results suggest that B
LyS may be a useful marker for early activation of an autoimmune diathesis
and likely plays a critical role in triggering activation of self-hg-driven
autoimmune B cells in human SLE. BLyS may provide an effective therapeutic
target in systemic autoimmunity.