BLyS: Member of the Tumor Necrosis Factor Family and B Lymphocyte Stimulator

Paul A. Moore(Human Genome Sciences (United States)), Ornella Belvedere(Human Genome Sciences (United States)), A. S. ORR(Human Genome Sciences (United States)), Krystyna Pieri(Human Genome Sciences (United States)), David W. LaFleur(Human Genome Sciences (United States)), Ping Feng(Human Genome Sciences (United States)), Daniel Soppet(Human Genome Sciences (United States)), Meghan Charters(Human Genome Sciences (United States)), Reiner Gentz(Human Genome Sciences (United States)), David C. Parmelee(Human Genome Sciences (United States)), Yuling Li(Human Genome Sciences (United States)), Olga Galperina(Human Genome Sciences (United States)), Judith G. Giri(Human Genome Sciences (United States)), Viktor Roschke(Human Genome Sciences (United States)), Bernardetta Nardelli(Human Genome Sciences (United States)), Jeffrey A. Carrell(Human Genome Sciences (United States)), Svetlana Sosnovtseva(Human Genome Sciences (United States)), Wilbert Greenfield(Human Genome Sciences (United States)), Steven M. Ruben(Human Genome Sciences (United States)), Henrik S. Olsen(Human Genome Sciences (United States)), James Fikes(Human Genome Sciences (United States)), David M. Hilbert(Human Genome Sciences (United States))
Science
July 9, 1999
Cited by 1,149

Abstract

The tumor necrosis factor (TNF) superfamily of cytokines includes both soluble and membrane-bound proteins that regulate immune responses. A member of the human TNF family, BLyS (B lymphocyte stimulator), was identified that induced B cell proliferation and immunoglobulin secretion. BLyS expression on human monocytes could be up-regulated by interferon-γ. Soluble BLyS functioned as a potent B cell growth factor in costimulation assays. Administration of soluble recombinant BLyS to mice disrupted splenic B and T cell zones and resulted in elevated serum immunoglobulin concentrations. The B cell tropism of BLyS is consistent with its receptor expression on B-lineage cells. The biological profile of BLyS suggests it is involved in monocyte-driven B cell activation.


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