Recent Developments and Future Directions of Alloimmunization to Transfused Blood Products

被引:4
|
作者
Zimring, James C. [1 ]
机构
[1] Emory Univ, Sch Med, Ctr Transfus & Cellular Therapies, Dept Pathol & Lab Med, Atlanta, GA 30322 USA
关键词
Alloimmunization; Transfusion; Rejection; Immunity; SEVERE APLASTIC-ANEMIA; MINOR HISTOCOMPATIBILITY ANTIGENS; BONE-MARROW-TRANSPLANTATION; PLATELET ALLOIMMUNIZATION; INFLAMMATION; ANTIBODIES; FREQUENCY; REJECTION;
D O I
10.1016/j.cll.2010.02.012
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Monitoring and managing alloimmunization are among the primary functions of the clinical transfusion medicine laboratory. However, despite hundreds of different blood group antigens that vary from person to person, only a minority of transfusion recipients become alloimmunized. Currently, there are no tests that predict which patients will become alloimmunized. Moreover, there are no therapeutic interventions to prevent alloimmunization (outside of RhD immune globulin) besides phenotypic matching. Understanding the biologic factors that regulate alloimmunization may allow the generation of clinical tests with predictive capabilities and provide a rational basis for developing therapeutic interventions. This article summarizes recent advances in understanding alloimmunization, with a focus of identifying future directions in laboratory testing and management of transfusion. In addition to analyzing humoral alloimmunization, potential extensions of transfusion medicine to sequelae of cellular immunization are explored.
引用
收藏
页码:467 / +
页数:9
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