Herpesvirus Entry Mediator Ligand (HVEM-L), a Novel Ligand for HVEM/TR2, Stimulates Proliferation of T Cells and Inhibits HT29 Cell Growth

Jeremy Harrop, Peter McDonnell(CSL (United States)), Michael Brigham‐Burke(CSL (United States)), Sally D. Lyn(CSL (United States)), Jayne A.L. Minton(CSL (United States)), K. B. Tan(Plant Gene Expression Center), Kim Dede, Jay Spampanato, Carol Silverman(New Frontier), Preston Hensley(CSL (United States)), Rocco DiPrinzio, John G. Emery(CSL (United States)), Keith C. Deen, Christopher Eichman, Marie Chabot‐Fletcher(CSL (United States)), Alemseged Truneh, Peter R. Young(CSL (United States))
Journal of Biological Chemistry
October 1, 1998
Cited by 241Open Access
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Abstract

Herpesvirus entry mediator (HVEM), a member of the tumor necrosis factor (TNF) receptor family, mediates herpesvirus entry into cells during infection. Upon overexpression, HVEM activates NF-kappaB and AP-1 through a TNF receptor-associated factor (TRAF)-mediated mechanism. Using an HVEM-Fc fusion protein, we screened soluble forms of novel TNF-related proteins derived from an expressed sequence tag data base. One of these, which we designated HVEM-L, specifically bound to HVEM-Fc with an affinity of 44 nM. This association was confirmed with soluble and membrane forms of both receptor and ligand. HVEM-L mRNA is expressed in spleen, lymph nodes, macrophages, and T cells and encodes a 240-amino acid protein. A soluble, secreted form of the protein stimulates proliferation of T lymphocytes during allogeneic responses, inhibits HT-29 cell growth, and weakly stimulates NF-kappaB-dependent transcription.


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