Immune tolerance induction with antihaemophilia factor (human) in poor prognosis patients with haemophilia A.
Mark H. Holguin, M.D.
Escobar, M., Shaffer, L., Holguin, M., McCavit, T., Amega, N.S. and Rajan, S.K. (2021). “Immune tolerance induction with antihaemophilia factor (human) in poor prognosis patients with haemophilia A.” Haemophilia Feb 3. [Epub ahead of print].
The formation of inhibitors (neutralizing antibodies) to factor VIII (FVIII) is a serious complication of haemophilia A (FVIII deficiency).1 Since the 1970s, immune tolerance induction (ITI) therapy using repeated dosing with FVIII concentrates has remained the standard of care to eradicate inhibitors.2 Although the non‐factor, bispecific monoclonal antibody emicizumab (approved by the Food and Drug Administration in 2017) was shown effective as prophylaxis to significantly reduce bleeding in patients with haemophilia A and inhibitors,3, 4 it does not prevent bleeds completely.2 Thus, most clinicians treating haemophilia still recommend that patients with inhibitors receive at least one round of ITI. [No abstract; excerpt from article].