BAFF, a Novel Ligand of the Tumor Necrosis Factor Family, Stimulates B Cell Growth

Author:

Schneider Pascal1,MacKay Fabienne1,Steiner Véronique1,Hofmann Kay1,Bodmer Jean-Luc1,Holler Nils1,Ambrose Christine1,Lawton Pornsri1,Bixler Sarah1,Acha-Orbea Hans1,Valmori Danila1,Romero Pedro1,Werner-Favre Christiane1,Zubler Rudolph H.1,Browning Jeffrey L.1,Tschopp Jürg1

Affiliation:

1. From the Institute of Biochemistry, University of Lausanne and Swiss Institute for Experimental Cancer Research, BIL Research Centre, CH-1066 Epalinges, Switzerland; the Division for Clinical Onco-Immunology, Ludwig Institute for Cancer Research, CHUV, CH-1011 Lausanne, Switzerland; the Division of Haematology, Geneva University Hospital, CMU, 1211 Geneva 14, Switzerland; and Biogen, Inc., Depart

Abstract

Members of the tumor necrosis factor (TNF) family induce pleiotropic biological responses, including cell growth, differentiation, and even death. Here we describe a novel member of the TNF family, designated BAFF (for B cell activating factor belonging to the TNF family), which is expressed by T cells and dendritic cells. Human BAFF was mapped to chromosome 13q32-34. Membrane-bound BAFF was processed and secreted through the action of a protease whose specificity matches that of the furin family of proprotein convertases. The expression of BAFF receptor appeared to be restricted to B cells. Both membrane-bound and soluble BAFF induced proliferation of anti-immunoglobulin M–stimulated peripheral blood B lymphocytes. Moreover, increased amounts of immunoglobulins were found in supernatants of germinal center–like B cells costimulated with BAFF. These results suggest that BAFF plays an important role as costimulator of B cell proliferation and function.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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