- John W. Semple
John W. Semple is a Canadain Scientist at St. Michael's Hospital and a Professor of Pharmacology at the
University of Toronto . He was born inWindsor, Ontario in 1959 and received his PhD in Immunology atQueen's University atKingston, Ontario . In 1991, Semple, along with John Freedman, discovered aT helper cell defect in patients with the bleeding disorder called immune thrombocytopenicpurpura (ITP). [1] . ITP is the condition of having a lowplatelet count (thrombocytopenia) and most causes appear to be related toantibodies against platelets. Very low platelet counts can lead to a bleeding diathesis and purpura. The T cell defect was initially shown to be an exaggeratedinterleukin-2 response when T cells were cultured with platelets in vitro. Subsequently, thiscytokine abnormality was shown by others to be responsible for many of theautoimmune mechanisms causing the disorder. [2] [3] [4] [5] [6] The importance of understanding the T cell defects in ITP is that novel therapies aimed at these cells may significantly benefit patients with ITP.1. Semple JW et al. Increased antiplatelet T helper lymphocyte reactivity in patients with autoimmune thrombocytopenia. Blood 8:2619-2625.
2. Cooper N et al. The pathogenesis of immune thrombocytopaenic purpura. Brit J Haematol 2006;133:364–374.
3. Semple JW et al. Differences in serum cytokine levels in acute and chronic autoimmune thrombocytopenic purpura: relationship to platelet phenotype and antiplatelet T-cell reactivity. Blood 1996:87:4245-4254.
4. Kuwana M et al. Autoreactive T cells to platelet GPIIb-IIIa in immune thrombocytopenic purpura. Role in production of anti-platelet autoantibody. J Clin Invest 1998;102:1393-1402.
5. Olsson B et al. T-cell-mediated cytotoxicity toward platelets in chronic idiopathic thrombocytopenic purpura. Nature Medicine 2003;9:1123–1124.
6. Stasi R et al. Analysis of regulatory T cell changes in patients with idiopathic thrombocytopenic purpura receiving B-cell depleting therapy with rituximab. Blood 2008;112:1147-1150.
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