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T-cell co-stimulation through B7RP-1 and ICOS
Authors:Yoshinaga S K  Whoriskey J S  Khare S D  Sarmiento U  Guo J  Horan T  Shih G  Zhang M  Coccia M A  Kohno T  Tafuri-Bladt A  Brankow D  Campbell P  Chang D  Chiu L  Dai T  Duncan G  Elliott G S  Hui A  McCabe S M  Scully S  Shahinian A  Shaklee C L  Van G  Mak T W  Senaldi G
Institution:Amgen Inc., Thousand Oaks, California 91320, USA. syoshina@amgen.com
Abstract:T-cell activation requires co-stimulation through receptors such as CD28 and antigen-specific signalling through the T-cell antigen receptor. Here we describe a new murine costimulatory receptor-ligand pair. The receptor, which is related to CD28 and is the homologue of the human protein ICOS, is expressed on activated T cells and resting memory T cells. The ligand, which has homology to B7 molecules and is called B7-related protein-1 (B7RP-1), is expressed on B cells and macrophages. ICOS and B7RP-I do not interact with proteins in the CD28-B7 pathway, and B7RP-1 co-stimulates T cells in vitro independently of CD28. Transgenic mice expressing a B7RP-1-Fc fusion protein show lymphoid hyperplasia in the spleen, lymph nodes and Peyer's patches. Presensitized mice treated with B7RP-1-Fc during antigen challenge show enhanced hypersensitivity. Therefore, B7RP-1 exhibits co-stimulatory activities in vitro and in vivo. ICOS and B7RP-1 define a new and distinct receptor-ligand pair that is structurally related to CD28-B7 and is involved in the adaptive immune response.
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