Table 1.

ROTEM assay results using whole blood samples collected on day 140 after IO infusion of LVs to evaluate platelet FVIII function in HemA mice

MiceMean ± standard deviation of mean
CT, sCFT, sα, degreeMCF, mm
G-F8/N6K12RH-LV + drugs 146 ± 4* 104 ± 21 70 ± 4** 66 ± 4 
G-F8/N6K12RH-LV 388 ± 193 165 ± 123 62 ± 15* 61 ± 7 
G-F8/N6-LV 564 ± 367 261 ± 182 43 ± 13 62 ± 6 
Wild type 164 ± 49* 57 ± 10* 79 ± 2** 63 ± 1 
HemA 956 ± 185* 2370 ± 1150* 4 ± 6*** 26 ± 19* 
MiceMean ± standard deviation of mean
CT, sCFT, sα, degreeMCF, mm
G-F8/N6K12RH-LV + drugs 146 ± 4* 104 ± 21 70 ± 4** 66 ± 4 
G-F8/N6K12RH-LV 388 ± 193 165 ± 123 62 ± 15* 61 ± 7 
G-F8/N6-LV 564 ± 367 261 ± 182 43 ± 13 62 ± 6 
Wild type 164 ± 49* 57 ± 10* 79 ± 2** 63 ± 1 
HemA 956 ± 185* 2370 ± 1150* 4 ± 6*** 26 ± 19* 

Each assay was carried out for 1 h to obtain values of clotting time (CT), clot formation time (CFT), α angle, and maximum clot firmness (MCF). Statistical significance was analyzed based on relevance to G-F8/N6-LV–treated mouse group. Mice were treated with G-F8/N6K12RH-LV + drugs, G-F8/N6K12RH-LV, or G-F8/N6-LV. Untreated wild-type normal mice and HemA mice were used as positive and negative controls, respectively.

*

P < .05, **P < .01, ***P < .001.

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