Figure 1
Figure 1. The immunogenicity of platelets that contain FVIII in naïve FVIIInull mice. Platelets isolated from transgenic mice (2bF8Tg), in which FVIII expression was driven by the platelet-specific αIIb promoter, were infused into FVIIInull mice without any preconditioning. The transgenic platelets were transfused to a level between 18% and 56% of total platelets upon infusion. (A) Schematic diagram of platelet transfusion in naïve FVIIInull mice. (B) Tail-clipping test on FVIIInull mice after transfusion of 2bF8Tg platelets. Tail-clipping test was performed 1 day after platelet infusion to assess phenotypic correction of FVIIInull coagulation defect. (C) The levels of platelet-FVIII in transfused recipients. Platelets were collected 1 week after platelet infusion, and functional FVIII activity levels were determined by a chromogenic assay on platelet lysates. (D) The inhibitor titers in recipients after infusion of 2bF8Tg platelets or rhF8. The anti-FVIII inhibitor titers were determined by Bethesda assay. (E) The total anti-FVIII immunoglobulin (Ig) G titers in recipients after infusion of 2bF8Tg platelets or rhF8. The total anti-FVIII IgG titers were determined by ELISA assay. These results demonstrate that transfusion of platelets containing FVIII into naïve FVIIInull mice neither elicits an anti-FVIII immune response nor induces immune suppression. FD, full dose; Wks, weeks.

The immunogenicity of platelets that contain FVIII in naïve FVIIInull mice. Platelets isolated from transgenic mice (2bF8Tg), in which FVIII expression was driven by the platelet-specific αIIb promoter, were infused into FVIIInull mice without any preconditioning. The transgenic platelets were transfused to a level between 18% and 56% of total platelets upon infusion. (A) Schematic diagram of platelet transfusion in naïve FVIIInull mice. (B) Tail-clipping test on FVIIInull mice after transfusion of 2bF8Tg platelets. Tail-clipping test was performed 1 day after platelet infusion to assess phenotypic correction of FVIIInull coagulation defect. (C) The levels of platelet-FVIII in transfused recipients. Platelets were collected 1 week after platelet infusion, and functional FVIII activity levels were determined by a chromogenic assay on platelet lysates. (D) The inhibitor titers in recipients after infusion of 2bF8Tg platelets or rhF8. The anti-FVIII inhibitor titers were determined by Bethesda assay. (E) The total anti-FVIII immunoglobulin (Ig) G titers in recipients after infusion of 2bF8Tg platelets or rhF8. The total anti-FVIII IgG titers were determined by ELISA assay. These results demonstrate that transfusion of platelets containing FVIII into naïve FVIIInull mice neither elicits an anti-FVIII immune response nor induces immune suppression. FD, full dose; Wks, weeks.

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