Plasma-derived versus recombinant Factor VIII concentrates for the treatment of haemophilia A: recombinant is better

被引:0
作者
Franchini, Massimo [1 ]
机构
[1] Azienda Osped Univ Parma, Serv Immunoematol & Trasfus, Parma, Italy
关键词
PREVIOUSLY UNTREATED PATIENTS; IMMUNE TOLERANCE INDUCTION; INHIBITOR DEVELOPMENT; CHILDREN; PURITY; EPIDEMIOLOGY; PRODUCTS; EFFICACY; COMPLEX; RISK;
D O I
10.2450/2010.0067.10
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:292 / 296
页数:5
相关论文
共 48 条
[1]  
ADDIEGO JE, 1992, THROMB HAEMOSTASIS, V67, P19
[2]   Overview of inhibitors [J].
Astermark, Jan .
SEMINARS IN HEMATOLOGY, 2006, 43 (02) :S3-S7
[3]  
Auerswald G, 2003, Haematologica, V88
[4]   Immune tolerance and the immune modulation protocol [J].
Berntorp, E ;
Nilsson, IM .
VOX SANGUINIS, 1996, 70 :36-41
[5]  
BRIET E, 1994, THROMB HAEMOSTASIS, V72, P162
[6]   Early factor VIII exposure and subsequent inhibitor development in children with severe haemophilia A [J].
Chalmers, E. A. ;
Brown, S. A. ;
Keeling, D. ;
Liesner, R. ;
Richards, M. ;
Stirling, D. ;
Thomas, A. ;
Vidler, V. ;
Williams, M. D. ;
Young, D. .
HAEMOPHILIA, 2007, 13 (02) :149-155
[7]   Assessing risk factors: prevention of inhibitors in haemophilia [J].
Chambost, H. .
HAEMOPHILIA, 2010, 16 :10-15
[8]   Prophylaxis in people with haemophilia [J].
Coppola, Antonio ;
Franchini, Massimo ;
Tagliaferri, Annarita .
THROMBOSIS AND HAEMOSTASIS, 2009, 101 (04) :674-681
[9]   VWF protects FVIII from endocytosis by dendritic cells and subsequent presentation to immune effectors [J].
Dasgupta, Suryasarathi ;
Repesse, Yohann ;
Bayry, Jagadeesh ;
Navarrete, Ana-Maria ;
Wootla, Bharath ;
Delignat, Sandrine ;
Irinopoulou, Theano ;
Kamate, Caroline ;
Saint-Remy, Jean-Marie ;
Jacquemin, Marc ;
Lenting, Peter J. ;
Borel-Derlon, Annie ;
Kaveri, Srinivas V. ;
Lacroix-Desmazes, Sebastien .
BLOOD, 2007, 109 (02) :610-612
[10]   International workshop on immune tolerance induction: consensus recommendations [J].
Dimichele, D. M. ;
Hoots, W. K. ;
Pipe, S. W. ;
Rivard, G. E. ;
Santagostino, E. .
HAEMOPHILIA, 2007, 13 :1-22