Cellular immune mechanisms in autoimmune thrombocytopenic purpura: An update

被引:85
作者
Coopamah, MD
Garvey, MB
Freedman, J
Semple, JW
机构
[1] St Michaels Hosp, Dept Lab Med & Pathobiol, Toronto, ON M5B 1W8, Canada
[2] Univ Toronto, Dept Pharmacol, Canadian Blood Serv, Toronto, ON, Canada
[3] Univ Toronto, Dept Med & Lab Med, Canadian Blood Serv, Toronto, ON, Canada
[4] Univ Toronto, Dept Pathobiol, Canadian Blood Serv, Toronto, ON, Canada
[5] Toronto Platelet Immunobiol Grp, Toronto, ON, Canada
关键词
D O I
10.1053/tmrv.2003.50004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Autoimmune thrombocytopenic purpura (AITP) is a bleeding disorder in which autoantibodies are directed against an individual's own platelets, leading to enhanced clearance through Fc receptor (R)-mediated phagocytosis by macrophages residing in the reticuloendothelial system (RES), particularly in the spleen. The production of IgG autoantibodies is critically dependent on cellular immune mechanisms particularly relating to T cells. We review the recent literature of the cell-mediated immunology of AITP focusing on platelet phenotype, genetics, T-cell reactivities, and cytokine profiles in patients with AITP. Understanding the interaction between these cell-mediated mechanisms is vital for developing antigen specific immunotherapies to treat this autoimmune disease. Copyright 2003, Elsevier Science (USA). All rights reserved.
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页码:69 / 80
页数:12
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