Table 1

Estimated prevalence of FVIII-binding antibodies in healthy individuals and in different patient cohorts

Patient typeSample sizePrevalence of positive individuals, % (95% CI)Prevalence of antibodies with titers ≥ 1:80, % (95% CI)Prevalence of antibodies with titers < 1:80, % (95% CI)
Healthy 600 19 (16-22) 2 (1-4) 17 (14-20) 
Severe hemophilia A without inhibitor (HA-no/INH) 77 34 (24-45) 5 (2-13) 31 (22-42) 
Severe hemophilia A after successful ITI (HA-ITI) 23 39 (22-59) 4 (1-21) 35 (19-55) 
Severe hemophilia A with inhibitor (HA-INH) 20 100 (84-100) 100 (84-100) 0 (0-16) 
Acquired hemophilia A (Acqu-HA) 100 (70-100) 100 (70-100) 0 (0-30) 
Patient typeSample sizePrevalence of positive individuals, % (95% CI)Prevalence of antibodies with titers ≥ 1:80, % (95% CI)Prevalence of antibodies with titers < 1:80, % (95% CI)
Healthy 600 19 (16-22) 2 (1-4) 17 (14-20) 
Severe hemophilia A without inhibitor (HA-no/INH) 77 34 (24-45) 5 (2-13) 31 (22-42) 
Severe hemophilia A after successful ITI (HA-ITI) 23 39 (22-59) 4 (1-21) 35 (19-55) 
Severe hemophilia A with inhibitor (HA-INH) 20 100 (84-100) 100 (84-100) 0 (0-16) 
Acquired hemophilia A (Acqu-HA) 100 (70-100) 100 (70-100) 0 (0-30) 

Estimated prevalence of FVIII-binding antibodies in healthy individuals, in patients with hemophilia A without inhibitors, and in patients with hemophilia A after successful immune tolerance induction therapy (ITI). Some samples contained more than one population of antibodies of different Ig isotypes and IgG subclasses which were individually assessed for antibody titers ≥ 1:80 and antibody titers < 1:80, respectively. Therefore, the prevalence of antibody titers ≥ 1:80 and antibody titers < 1:80 does not necessarily add up to the total prevalence of positive individuals.

FVIII indicates factor VIII; and CI, confidence interval.

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