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From the Department of Pathology, School of Medicine, University of North Carolina, Chapel Hill.
Correspondence to William E. Sanders, Jr, MD, Division of Cardiology, CB #7075, Burnett-Womack Bldg, University of North Carolina Hospitals, Chapel Hill, NC 27599-7075.
Abstract Thrombotic thrombocytopenia with severe depletion of
plasma von Willebrand factor (vWF) was induced in normal large animals
(5 dogs and 2 pigs) by botrocetin, a Bothrops factor
requiring vWF for platelet agglutination. Botrocetin (90 to 100 U/kg,
2.14 to 2.38 mg/kg, in a single IV injection) reduced plasma vWF
activity to <0.1 U/mL for 24 hours. During this period, multimeric
analysis of plasma vWF antigen (Ag) revealed the loss of
intermediate- and high-molecular-weight forms with a concomitant
increase in lower molecular weight forms. A moderate reduction in
factor VIII (FVIII) activity was observed. The vWF reduction was
accompanied by transient thrombocytopenia and prolonged bleeding times
during the deficiency state. Occlusive platelet thrombi were detected
by transmission electron microscopy in the microcirculation of lung and
spleen but not kidney or brain 30 minutes after the botrocetin
injection. Recovery of plasma vWF and platelet count occurred within 48
hours and was associated with the appearance in the plasma of unusually
large forms of vWF:Ag multimers. The vWF:Ag multimer distribution was
normal at 72 hours. The ultrastructural distribution of vWF in
unstimulated normal porcine and canine platelets was examined by using
immunogold staining. VWF was detected in the
-granules of normal pig
platelets but was not observed in platelets from normal dogs. However,
both animals developed thrombotic thrombocytopenia when injected with
botrocetin. A second group of animals (2 dogs and 3 pigs) with von
Willebrand disease (vWD) was given a single botrocetin injection (90 to
100 U/kg). No thrombocytopenia occurred. Electron photomicrographs
showed no platelet thrombi in any tissues examined. Porcine and canine
platelets from vWD animals exhibited no specific labeling of vWF in any
-granule. The vWD animals were entirely protected from the
thrombocytopenia and thrombogenic action of botrocetin. These data
suggest that plasma vWF but not platelet vWF is required for the
intravascular platelet and microthrombotic response and that the
thrombotic thrombocytopenic syndrome cannot be induced in the absence
of plasma vWF.
Key Words: thrombotic thrombocytopenia thrombotic thrombocytopenic purpura von Willebrand disease von Willebrand factor
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