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      Prevention of organ allograft rejection by a specific Janus kinase 3 inhibitor.

      Science (New York, N.Y.)
      Animals, Enzyme Inhibitors, administration & dosage, pharmacology, therapeutic use, toxicity, Gene Expression Regulation, drug effects, Graft Rejection, prevention & control, Graft Survival, Heart Transplantation, Humans, Immunosuppressive Agents, Interleukin-2, immunology, Janus Kinase 3, Kidney Transplantation, Lymphocyte Activation, Lymphocyte Count, Lymphocyte Culture Test, Mixed, Lymphocyte Subsets, Macaca fascicularis, Mice, Mice, Inbred C57BL, Mice, Inbred DBA, Myocardium, metabolism, Piperidines, Protein-Tyrosine Kinases, antagonists & inhibitors, Pyrimidines, Pyrroles, Transplantation, Heterotopic, Transplantation, Homologous, Tumor Cells, Cultured

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          Abstract

          Because of its requirement for signaling by multiple cytokines, Janus kinase 3 (JAK3) is an excellent target for clinical immunosuppression. We report the development of a specific, orally active inhibitor of JAK3, CP-690,550, that significantly prolonged survival in a murine model of heart transplantation and in cynomolgus monkeys receiving kidney transplants. CP-690,550 treatment was not associated with hypertension, hyperlipidemia, or lymphoproliferative disease. On the basis of these preclinical results, we believe JAK3 blockade by CP-690,550 has potential for therapeutically desirable immunosuppression in human organ transplantation and in other clinical settings.

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