Summary
Use of high purity and recombinant factor VIII (FVIII) concentrates has been thought
to be associated with an increased incidence of FVIII inhibitors in patients with
severe haemophilia A. Comparison with comparable historical control groups has suggested
that the true incidence of inhibitors in patients with severe haemophilia A was ~20-25%,
similar to the incidence seen with new high purity and recombinant FVIII products.
We have conducted a study of inhibitor development in a cohort of 37 boys with severe
haemophilia A (VIII: C <2 u/dl) exposed only to a single FVIII concentrate (BPL 8Y)
with no previous blood or blood product exposure. This factor VIII concentrate is
an intermediate purity product with a specific activity of ~2 IU/mg protein and contains
well preserved von Willebrand factor multimers. It is manufactured by conventional
fractionation technologies and terminally dry heat treated at 80° C for 72 h.