T-cell co-stimulation through B7RP-1 and ICOS

SK Yoshinaga, JS Whoriskey, SD Khare, U Sarmiento… - Nature, 1999 - nature.com
SK Yoshinaga, JS Whoriskey, SD Khare, U Sarmiento, J Guo, T Horan, G Shih, M Zhang…
Nature, 1999nature.com
T-cell activation requires co-stimulation through receptors such as CD28 (refs,,) and antigen-
specific signalling through the T-cell antigen receptor. Here we describe a new murine co-
stimulatory 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-1 do not …
Abstract
T-cell activation requires co-stimulation through receptors such as CD28 (refs ,,) and antigen-specific signalling through the T-cell antigen receptor. Here we describe a new murine co-stimulatory 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-1 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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