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BAFF overexpression in lupus may be blockable with decoy receptor, monoclonal.

Vaccine Weekly

| December 10, 2003 | COPYRIGHT 2003 NewsRX. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

2003 DEC 10 - (NewsRx.com & NewsRx.net) -- In lupus erythematosus, excess BAFF expression may be curbed by treatment with decoy BAFF receptor or with monoclonal antibodies; may stop symptoms.

"BAFF, a member of the family of tumor necrosis factor (TNF) ligands, is essential for the development of peripheral mature, long lived B lymphocytes. It binds to three different receptors, BCMA, TACI, and BAFF-R, which are all members of the family of TNF receptors. Defects in the genes encoding BAFF or BAFF-R abolish the generation of mature B cells," scientists in Switzerland report.

"BAFF is made by myeloid cells, whereas BAFF-R is expressed preferentially on B cells. BAFF induces polyclonal maturation of resting, short lived, immature B cells into resting, long-lived, mature B cells, without proliferation. Lupus-prone mice have elevated blood levels of BAFF, and treatment of these mice with the BAFF decoy receptor (BCMA-Ig) prevents the onset of this systemic autoimmune disease," wrote F. Melchers and colleagues from the University of Basel.

The researchers concluded: "Human lupus ...

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