Inhibitor treatment in haemophilias A and B: inhibitor diagnosis

被引:18
作者
Dimichele, D. M. [1 ]
机构
[1] Cornell Univ, Dept Pediat & Publ Hlth, Weill Med Coll, New York, NY 10021 USA
关键词
Bethesda assay; clinical surveillance; inhibitors; Nijmegen assay;
D O I
10.1111/j.1365-2516.2006.01364.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The clinical diagnosis and quantitative measurement of polyclonal IgG inhibiting antibodies are the subjects of this review. Inhibitors in congenital haemophilia are usually diagnosed either as part of a routine surveillance schedule or following a bleeding episode that responds poorly to standard specific replacement therapy. Routine surveillance schedules for paediatric haemophilia A patients during high-risk incidence periods are variable and the subject of ongoing discussion. There have never been any published recommendations for following haemophilia B patients at high risk for inhibitor development. The Factor VIII/IX Subcommittee of the International Society on Thrombosis and Haemostasis scientifically endorsed the Nijmegen method for inhibitor measurement in 1996. However, there are many unresolved issues surrounding inhibitor diagnosis using these assays. These issues include: (i) questions of accuracy and inter-assay variability inherent to the one-stage clotting assay; (ii) lack of consensus regarding the assay cut-off for negative determination; (iii) lack of assay standardization and (iv) the clinical importance of capturing non-neutralizing antibodies currently not measured in the functional assays. Ongoing efforts to resolve these issues will be discussed.
引用
收藏
页码:37 / 41
页数:5
相关论文
共 35 条
[1]   FREQUENCY OF INHIBITOR DEVELOPMENT IN HEMOPHILIACS TREATED WITH LOW-PURITY FACTOR-VIII [J].
ADDIEGO, J ;
KASPER, C ;
ABILDGAARD, C ;
HILGARTNER, M ;
LUSHER, J ;
GLADER, B ;
ALEDORT, L .
LANCET, 1993, 342 (8869) :462-464
[2]  
ADDIEGO JE, 1992, THROMB HAEMOSTASIS, V67, P19
[3]  
[Anonymous], FACTOR 8 INHIBITORS
[4]   Impact of inhibitor epitope profile on the neutralizing effect against plasma-derived and recombinant factor VIII concentrates in vitro [J].
Astermark, J ;
Voorberg, J ;
Lenk, H ;
Dimichele, D ;
Shapiro, A ;
Tjönnfjord, G ;
Berntorp, E .
HAEMOPHILIA, 2003, 9 (05) :567-572
[5]   Variation in factor VIII inhibitor reactivity with different commercial factor VIII preparations [J].
Berntorp, E ;
Ekman, M ;
Gunnarsson, M ;
Nilsson, IM .
HAEMOPHILIA, 1996, 2 (02) :95-99
[6]  
BRAY GL, 1994, BLOOD, V83, P2428
[7]  
BRIET E, 1991, BLOOD COAGUL FIBRIN, V2, P47
[8]  
DEBIASI R, 1994, THROMB HAEMOSTASIS, V71, P544
[9]  
Dimichele D, 2005, TXB HEMOPHILIA, P64
[10]   INCIDENCE OF DEVELOPMENT OF FACTOR-VIII AND FACTOR-IX INHIBITORS IN HEMOPHILIACS [J].
EHRENFORTH, S ;
KREUZ, W ;
SCHARRER, I ;
LINDE, R ;
FUNK, M ;
GUNGOR, T ;
KRACKHARDT, B ;
KORNHUBER, B .
LANCET, 1992, 339 (8793) :594-598