A human antibody that inhibits factor IX/IXa function potently inhibits arterial thrombosis without increasing bleeding

被引:25
作者
Refino, CJ [1 ]
Jeet, S [1 ]
DeGuzman, L [1 ]
Bunting, S [1 ]
Kirchhofer, D [1 ]
机构
[1] Genentech Inc, Dept Physiol, San Francisco, CA 94080 USA
关键词
thrombosis; factor IX; anticoagulants; antibody;
D O I
10.1161/hq0302.105375
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
10C12, a human antibody F(ab')(2), which specifically binds to the gamma-carboxyglutamic acid domain of factor IX/factor IXa (FIX/IXa), interferes with all known coagulation processes in which F.IX/IXa is involved. In a rabbit model of carotid artery injury, intravenous administration of 10C12 or heparin decreased thrombosis dose dependently. The dose that resulted in a 90% reduction of thrombus mass (ED90) was a 30-mug/kg bolus of 10C12 or a 100-U/kg bolus plus 1.0 U . kg(-1) . min(-1) infusion of heparin. Heparin, at and below the ED90, significantly prolonged coagulation times and cuticle bleeding times. In contrast, 10C12 had no effect on coagulation or bleeding times at doses up to 4 times the ED90. To further evaluate the effect of 10C12 on bleeding, it was compared with heparin in a novel model of blood loss. At the ED90, of heparin, blood loss induced by a standardized injury to the vasculature of the rabbit tibia increased to more than 2 times that of saline controls. In contrast, the dose of 10C12 required to produce a similar increase in blood loss was more than 30 times the ED90. The antithrombotic potency and relative safety of this fully human antibody suggests that it may have therapeutic value for treatment of thrombotic disorders.
引用
收藏
页码:517 / 522
页数:6
相关论文
共 22 条
[1]   Coagulation factor IX residues G4-Q11 mediate its interaction with a shared factor IX/IXa binding site on activated platelets but not the assembly of the functional factor X activating complex [J].
Ahmad, SS ;
Wong, MY ;
Rawala, R ;
Jameson, BA ;
Walsh, PN .
BIOCHEMISTRY, 1998, 37 (06) :1671-1679
[2]   HIGH-AFFINITY, SPECIFIC FACTOR IXA BINDING TO PLATELETS IS MEDIATED IN PART BY RESIDUES-3-11 [J].
AHMAD, SS ;
RAWALASHEIKH, R ;
CHEUNG, WF ;
JAMESON, BA ;
STAFFORD, DW ;
WALSH, PN .
BIOCHEMISTRY, 1994, 33 (40) :12048-12055
[3]   PLATELET MEMBRANE-MEDIATED COAGULATION PROTEASE COMPLEX ASSEMBLY [J].
AHMAD, SS ;
WALSH, PN .
TRENDS IN CARDIOVASCULAR MEDICINE, 1994, 4 (06) :271-278
[4]   ACTIVE SITE-BLOCKED FACTOR-IXA PREVENTS INTRAVASCULAR THROMBUS FORMATION IN THE CORONARY VASCULATURE WITHOUT INHIBITING EXTRAVASCULAR COAGULATION IN A CANINE THROMBOSIS MODEL [J].
BENEDICT, CR ;
RYAN, J ;
WOLITZKY, B ;
RAMOS, R ;
GERLACH, M ;
TIJBURG, P ;
STERN, D .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (05) :1760-1765
[5]  
BRETTLER DB, 1994, HEMOSTASIS THROMBOSI, P169
[6]  
CHEUNG WF, 1992, J BIOL CHEM, V267, P20529
[7]  
Elg M, 1997, THROMB HAEMOSTASIS, V78, P1286
[8]  
Feuerstein GZ, 1999, THROMB HAEMOSTASIS, V82, P1443
[9]   Antithrombotic efficacy of a novel murine antihuman factor IX antibody in rats [J].
Feuerstein, GZ ;
Patel, A ;
Toomey, JR ;
Bugelski, P ;
Nichols, AJ ;
Church, WR ;
Valocik, R ;
Koster, P ;
Baker, A ;
Blackburn, MN .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (10) :2554-2562
[10]   STRUCTURE OF THE CALCIUM ION-BOUND GAMMA-CARBOXYGLUTAMIC ACID-RICH DOMAIN OF FACTOR-IX [J].
FREEDMAN, SJ ;
FURIE, BC ;
FURIE, B ;
BALEJA, JD .
BIOCHEMISTRY, 1995, 34 (38) :12126-12137