Circulation, Vol 87, 996-1006, Copyright © 1993 by American Heart Association
D Collen, F De Cock and JM Stassen
BACKGROUND. Streptokinase is a routinely used thrombolytic agent that is
immunogenic and relatively inefficient toward platelet-rich thrombus,
whereas staphylokinase is a poorly studied fibrinolytic agent. Here, the
comparative immunogenicity and thrombolytic properties toward arterial
platelet-rich thrombus and venous whole blood clots of streptokinase and
recombinant staphylokinase were studied in baboons. METHODS AND RESULTS.
The inhibitory capacity of baboon plasma (in a human plasma-based clot
lysis assay) was 0.39 +/- 0.25 microgram streptokinase and 0.04 +/- 0.05
microgram recombinant staphylokinase per milliliter of plasma (mean +/- SD,
n = 9). Intravenous infusion over 1 hour of 0.300 mg/kg of streptokinase at
0, 1, 2, 3, and 5 weeks in five baboons given heparin and the antiplatelet
agent ridogrel increased the streptokinase-neutralizing titer from 0.22 +/-
0.18 microgram/mL plasma at baseline to 3.8 +/- 4.4 micrograms/mL after 2
weeks (p = 0.043 versus baseline by Wilcoxon signed rank test) and to 4.4
+/- 4.6 micrograms/mL after 5 weeks, whereas the thrombolytic potency
toward a 125I-fibrin-labeled plasma clot inserted into an extracorporeal
arteriovenous loop was reduced from 84 +/- 7% at baseline to 45 +/- 8%
after 2 weeks and to 36 +/- 8% after 5 weeks (p < 0.01 versus baseline).
Administration over 1 hour of 0.065 mg/kg recombinant staphylokinase at 0,
1, 2, 3, and 5 weeks in four baboons did not induce measurable
staphylokinase-neutralizing activity in three of the four animals after 5
weeks. In the fourth baboon, a staphylokinase-neutralizing activity of 0.8
and 1.5 micrograms/mL was found at 3 and 5 weeks, respectively. Repeated
staphylokinase administration was not associated with inhibition of clot
lysis (43 +/- 4% lysis at baseline, 52 +/- 9% at 3 weeks, and 61 +/- 14% at
5 weeks; p = NS versus baseline). Repeated administration of streptokinase
but not of staphylokinase caused a marked (> 50%) decrease in blood
pressure, requiring administration of steroids and intravenous fluids, and
a marked increase in leukocyte count and hemoglobin concentration.
Intravenous infusion of streptokinase or recombinant staphylokinase over 1
hour in doses ranging between 0 and 1.0 mg/kg in three groups of four
baboons each induced dose-dependent lysis of a 125I-fibrin-labeled
autologous jugular vein blood clot (50% lysis requiring 0.140 mg/kg
streptokinase and 0.058 mg/kg recombinant staphylokinase, representing
equimolar amounts of 3.25 nmol/kg) without systemic fibrinogen depletion.
The thrombolytic potency toward platelet-rich arterial thrombus of
streptokinase and recombinant staphylokinase were studied in a femoral
arterial eversion graft model. Arterial recanalization with recombinant
staphylokinase was more frequent and more persistent than with
streptokinase (all p < 0.05). Intravenous infusion of 1.0 mg/kg
streptokinase or 0.25 mg/kg recombinant staphylokinase in two groups of
four baboons each given intravenous heparin (200-unit bolus and 50
units.kg-1 x hr-1) and aspirin (10 mg/kg) did not produce a significant
prolongation of the median template bleeding time. CONCLUSIONS. Recombinant
staphylokinase has a thrombolytic potency toward jugular vein blood clots
in baboons comparable to that of streptokinase, but it is less immunogenic
and less allergenic and it does not induce resistance to lysis upon
repeated administration; it is significantly more efficient than
streptokinase for the dissolution of platelet-rich arterial eversion graft
thrombi. Recombinant staphylokinase, which can be easily obtained in active
form by expression in Escherichia coli, may constitute a potentially useful
alternative to streptokinase for the treatment of acute myocardial
infarction.
ARTICLES
Comparative immunogenicity and thrombolytic properties toward arterial and venous thrombi of streptokinase and recombinant staphylokinase in baboons
Center for Thrombosis and Vascular Research, University of Leuven, Belgium.
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