Table 2.

Effect of MoAbs on vWF-Dependent CHO-GPIbβ/IX Cell Aggregation

MoAb CHO-GPIbαβ/IX Aggregation (%)
Buffer Ristocetin Heparin
None 4.2 ± 0.8  51.0 ± 1.0  48 ± 4.9  
Control antibody  3.1 ± 0.9  50.7 ± 0.9  47.8 ± 1.5 
6D1 (anti-GPIbα)  3.5 ± 1.2  5.3 ± 2.0* 8.5 ± 2.5* 
328 (anti-vWF)  5.8 ± 0.8 5.7 ± 3.7* 10.6 ± 2.7 
724 (anti-vWF) 7.8 ± 0.8  50.3 ± 1.2  17.8 ± 1.6 
MoAb CHO-GPIbαβ/IX Aggregation (%)
Buffer Ristocetin Heparin
None 4.2 ± 0.8  51.0 ± 1.0  48 ± 4.9  
Control antibody  3.1 ± 0.9  50.7 ± 0.9  47.8 ± 1.5 
6D1 (anti-GPIbα)  3.5 ± 1.2  5.3 ± 2.0* 8.5 ± 2.5* 
328 (anti-vWF)  5.8 ± 0.8 5.7 ± 3.7* 10.6 ± 2.7 
724 (anti-vWF) 7.8 ± 0.8  50.3 ± 1.2  17.8 ± 1.6 

CHO-GPIbαβ/IX cell aggregation was assessed at 6 cycles per second in the presence of 10 nmol/L vWF and either buffer, 1.4 mg/mL ristocetin or 100 μg/mL heparin. Cells were either preincubated with 20 μg/mL of control MoAb, 328, 724, or 6D1. The percentage of aggregated cells was calculated and the mean ± SEM was determined in 3 separate experiments. Statistical significance of differences between means was evaluated using the Student's t-test for paired samples by comparing aggregation in the presence of inhibitor versus the control corresponding sample in the absence of inhibitor.

*

P < .0025.

P < .05.

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