Inhibitor development: patient-determined risk factors

被引:48
作者
Astermark, J. [1 ]
机构
[1] Malmo Univ Hosp, Dept Coagulat Disorders, SE-20502 Malmo, Sweden
基金
瑞典研究理事会;
关键词
antibodies; haemophilia; inhibitors; MIBS; risk factors; siblings; NECROSIS-FACTOR-ALPHA; SYSTEMIC-LUPUS-ERYTHEMATOSUS; MALMO INTERNATIONAL BROTHER; CTLA-4; GENE; HEMOPHILIA-A; POLYMORPHISMS; INTERLEUKIN-10; ASSOCIATION; PATHOGENESIS; SECRETION;
D O I
10.1111/j.1365-2516.2008.01923.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The reasons that inhibitory factor VIII antibodies develop in only a fraction of patients with haemophilia A remain unclear, but studies of genetically related subjects have indicated that the immunological outcome of replacement therapy is to a large extent determined by patient-related risk factors. Non-genetic factors will also influence the inhibitor risk, since events challenging the immune system will elicit and stimulate immune regulatory processes with the potential of modifying the immune response. Further insight into the irnmuno-logical pathways and risk factors involved will be important in order to better predict and prevent this complication. This review will briefly summarize the data obtained to date in unrelated and related subjects in the Malmo International Brother Study (MIBS) regarding genetic factors and discuss how these factors might interact with non-genetically determined factors and events.
引用
收藏
页码:66 / 70
页数:5
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