Figure 4
Figure 4. Anticoagulant properties of anti-A2 mAbs. (A) Residual fVIII activity was measured by 1-stage coagulation assay following incubation of normal human plasma with varying concentrations of mAbs for 2 hours at 37°C. Data represent sample means and sample standard deviations. The curves represent least-squares fits to the data. The inhibitor titer in Bethesda units per milliter was obtained by determining the dilution of mAb producing 50% inhibition and converted to Bethesda units per milligram using the mAb concentration. (B) BDD human fVIII (50 nM) was incubated with the indicated concentrations of anti-A2 mAbs for 30 minutes and then thrombin for 60 seconds, followed by sample dilution into fIXa/PCPS phospholipid vesicles, addition of fX, and measurement of fXa as described in “Intrinsic fXase assay.” Results are presented as the percentage of fXa formed in the absence of mAb.

Anticoagulant properties of anti-A2 mAbs. (A) Residual fVIII activity was measured by 1-stage coagulation assay following incubation of normal human plasma with varying concentrations of mAbs for 2 hours at 37°C. Data represent sample means and sample standard deviations. The curves represent least-squares fits to the data. The inhibitor titer in Bethesda units per milliter was obtained by determining the dilution of mAb producing 50% inhibition and converted to Bethesda units per milligram using the mAb concentration. (B) BDD human fVIII (50 nM) was incubated with the indicated concentrations of anti-A2 mAbs for 30 minutes and then thrombin for 60 seconds, followed by sample dilution into fIXa/PCPS phospholipid vesicles, addition of fX, and measurement of fXa as described in “Intrinsic fXase assay.” Results are presented as the percentage of fXa formed in the absence of mAb.

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