Abstract
Autoimmune thrombocytopenic purpura (AITP) is a bleeding disease in which autoantibodies are directed against the individual's own platelets, resulting in enhanced Fc-mediated platelet destruction by macrophages in the reticuloendothelial system. Most research in AITP has focused on characterization of the autoantibodies, while little has been devoted to the cellular immune mechanisms leading to autoantibody production. This report summarizes the current state of the literature and argues that enhanced T helper cell/antigen-presenting cell interactions in patients with AITP are the primary stimulus for the development of antiplatelet autoantibody production. Understanding these events is important for eventually identifying disease-initiating platelet autoantigens and ultimately developing specific immunotherapies for AITP.
Original language | English |
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Pages (from-to) | 41-5 |
Journal | Acta Paediatrica, International Journal of Paediatrics, Supplement |
Volume | 424 |
DOIs | |
Publication status | Published - 1998 Jun |
Externally published | Yes |
Subject classification (UKÄ)
- Hematology
Free keywords
- Antigen-Presenting Cells/immunology
- Autoantigens/immunology
- Blood Platelets/immunology
- Humans
- Immunity, Cellular/immunology
- Purpura, Thrombocytopenic, Idiopathic/immunology
- T-Lymphocytes, Helper-Inducer/immunology