Detection of non inhibitory binding antibodies to von Willebrand factor affecting the clearance of VWF:Ag in von Willebrand disease

被引:0
作者
Suiter, T. M. [1 ]
Mannucci, P. M. [2 ]
Kempton, C. [3 ,4 ]
Laffan, M. [5 ]
Romond, E. H. [6 ]
Shapiro, A. [7 ]
Birschmann, I. [8 ]
Ragni, M. V. [9 ,10 ]
Gill, J. C. [11 ]
Yee, T. T. [12 ,13 ]
Klamroth, R. [14 ]
Horling, F. M. [15 ]
Reipert, B. M. [15 ]
Turecek, P. L. [1 ]
Varadi, K. [1 ]
Chapman, M. [1 ]
Engl, W. [1 ]
Wong, W. Y.
Ewenstein, B. M.
机构
[1] Baxter Innovat GmbH, Vienna, Austria
[2] Univ Milan, A Bianchi Bonomi Hemophilia & Thrombosis Ctr, I-20122 Milan, Italy
[3] Emory Univ, Sch Med, Dept Pediat, Atlanta, GA USA
[4] Emory Univ, Sch Med, Dept Hematol Oncol, Atlanta, GA USA
[5] Hammersmith Hosp, Imperial Coll Sch Med, Dept Hematol, London, England
[6] Univ Kentucky, Hemophilia Treatment Ctr, Lexington, KY 40506 USA
[7] Indiana Hemophilia & Thrombosis Ctr, Indiana, PA USA
[8] Hannover Med Sch, Dept Hematol Hemostasis Oncol & Stem Cell Transpl, D-3000 Hannover, Germany
[9] Univ Pittsburgh, Pittsburg, KS USA
[10] Hemophilia Ctr Western Penn, Dept Med, Div Hematol Oncol, Pittsburg, KS USA
[11] Med Coll Wisconsin, Milwaukee, WI 53226 USA
[12] Royal Free Hosp, Haemophilia Ctr, London NW3 2QG, England
[13] Royal Free Hosp, Thrombosis Unit, London NW3 2QG, England
[14] Vivantes Klinikum Friedrichshain, Klin Innere Med Angiol & Haemostaseol, Berlin, Germany
[15] Baxter BioSci, Immunol, Vienna, Austria
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:42 / 43
页数:2
相关论文
共 50 条
[31]   A mutation in the D4 domain of von Willebrand factor (VWF) results in a variant of type 1 von Willebrand disease with accelerated in vivo VWF clearance. [J].
Gavazova, S ;
Gill, JC ;
Scott, JP ;
Hillery, CA ;
Friedman, KD ;
Wetzel, N ;
Jozwiak, M ;
Haberichter, SL ;
Christopherson, P ;
Montgomery, RR .
BLOOD, 2002, 100 (11) :128A-128A
[32]   Acquired von Willebrand disease: potential contribution of the von Willebrand factor collagen-binding to the identification of functionally inhibiting auto-antibodies to von Willebrand factor: a rebuttal [J].
Guerin, V. ;
Ryman, A. ;
Velez, F. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2008, 6 (06) :1051-1052
[33]   The challenging management of a child with type 3 von Willebrand disease and antibodies to von Willebrand factor [J].
Pergantou, H. ;
Xafaki, P. ;
Adamtziki, E. ;
Koletsi, P. ;
Komitopoulou, A. ;
Platokouki, H. .
HAEMOPHILIA, 2012, 18 (03) :e66-e67
[34]   Von Willebrand Factor and von Willebrand disease: prerequisite for diagnostic [J].
Fressinaud, Edith .
HEMATOLOGIE, 2014, 20 :6-13
[35]   von Willebrand disease and quantitative variation in von Willebrand factor [J].
Mohlke, KL ;
Ginsburg, D .
JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 1997, 130 (03) :252-261
[36]   Comparison between plasma von Willebrand factor (VWF) and VWF antigen II level in normal individuals and patients with von Willebrand disease [J].
DeRomeuf, C ;
Mazurier, C .
BRITISH JOURNAL OF HAEMATOLOGY, 1996, 93 :640-640
[37]   Von Willebrand factor's clearance [J].
Denis, Cecile V. ;
Lenting, Peter J. .
HEMATOLOGIE, 2006, 12 (01) :34-43
[38]   The Y/C1584 mutation of von Willebrand factor in type 2M von willebrand disease: frequency and clearance of von Willebrand factor [J].
Millar, CM ;
Riddel, AF ;
Griffioe, A ;
Jenkin, PV ;
Brown, SA .
BRITISH JOURNAL OF HAEMATOLOGY, 2005, 130 (03) :462-463
[39]   The role of VWF:Ag II in patients with acquired von Willebrand disease [J].
Krause, M ;
Caron, C ;
Stier-Brück, I ;
Vigh, T ;
Scharrer, I .
34th Hemophilia Symposium, 2005, :207-211
[40]   INHIBITION OF WILLEBRAND FACTOR IN VON WILLEBRAND DISEASE [J].
MARAGALL, S ;
CASTILLO, R ;
ORDINAS, A ;
LIENDO, F ;
RODRIGUEZ, M .
THROMBOSIS RESEARCH, 1979, 14 (2-3) :495-500