Nature 2001 Jan
Dong C, Juedes AE, Temann UA, Shresta S, Allison JP, Ruddle NH, Flavell RA
Abstract
T-lymphocyte activation and immune function are regulated by co-stimulatory molecules. CD28, a receptor for B7 gene products, has a chief role in initiating T-cell immune responses. CTLA4, which binds B7 with a higher affinity, is induced after T-cell activation and is involved in downregulating T-cell responses. The inducible co-stimulatory molecule (ICOS), a third member of the CD28/CTLA4 family, is expressed on activated T cells. Its ligand B7H/B7RP-1 is expressed on B cells and in non-immune
...[more] tissues after injection of lipopolysaccharide into animals. To understand the role of ICOS in T-cell activation and function, we generated and analysed ICOS-deficient mice. Here we show that T-cell activation and proliferation are defective in the absence of ICOS. In addition, ICOS -/- T cells fail to produce interleukin-4 when differentiated in vitro or when primed in vivo. ICOS is required for humoral immune responses after immunization with several antigens. ICOS-/- mice showed greatly enhanced susceptibility to experimental autoimmune encephalomyelitis, indicating that ICOS has a protective role in inflammatory autoimmune diseases.
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Mesh Headings:
Amino Acid Sequence, Animals, Antibody Formation, Antigens, CD, Antigens, Differentiation, T-Lymphocyte, Cell Differentiation, Cells, Cultured, Encephalomyelitis, Autoimmune, Experimental, Gene Targeting, Hemocyanin, Inducible T-Cell Co-Stimulator Protein, Interleukin-13, Interleukin-4, Lymph Nodes, Lymphocyte Activation, Mice, Mice, Knockout, Molecular Sequence Data, Myelin Proteins, Myelin-Associated Glycoprotein, Myelin-Oligodendrocyte Glycoprotein, T-Lymphocytes