Increased cytotoxic T-lymphocyte-mediated cytotoxicity predominant in patients with idiopathic thrombocytopenic purpura without platelet autoantibodies
C. Zhao, X. Li, Feng Zhang, Lei Wang, Jun Peng, Ming Hou
Abstract
C. Zhao, X. Li, Feng Zhang, Lei Wang, Jun Peng, Ming Hou
Abstract
Idiopathic thrombocytopenic purpura (ITP) is a common hematologic disorder manifested by autoantibody-mediated platelet destruction. In the majority of ITP patients, autoantibodies were found to be specific to GPIIb/IIIa or GPIb/IX.[1][1] It may not only damage platelets via the reticuloendothelial
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Idiopathic thrombocytopenic purpura (ITP) is a common hematologic disorder manifested by autoantibody-mediated platelet destruction. In the majority of ITP patients, autoantibodies were found to be specific to GPIIb/IIIa or GPIb/IX.[1][1] It may not only damage platelets via the reticuloendothelial
Key concepts: Autoantibody, Platelet, Thrombocytopenic purpura, Medicine, Immunology, Mononuclear phagocyte system, Purpura (gastropod), Cytotoxic T cell