Table 3

Estimated prevalence of Ig isotypes and IgG subclasses of FVIII-binding antibodies found in healthy individuals and in different cohorts of hemophilia A patients

Study cohortSample sizeIgG1, %*IgG2, %*IgG3, %*IgG4, %*IgA, %*IgM, %*
Healthy 600 
Hemophilia A without inhibitor (HA-noINH) 77 19 13 
Hemophilia A after successful ITI (HA-ITI) 23 30 
Hemophilia A with inhibitor (HA-INH) 20 95 35 25 95 10 
Acquired hemophilia A (Acqu-HA) 100 67 22 100 11 11 
Study cohortSample sizeIgG1, %*IgG2, %*IgG3, %*IgG4, %*IgA, %*IgM, %*
Healthy 600 
Hemophilia A without inhibitor (HA-noINH) 77 19 13 
Hemophilia A after successful ITI (HA-ITI) 23 30 
Hemophilia A with inhibitor (HA-INH) 20 95 35 25 95 10 
Acquired hemophilia A (Acqu-HA) 100 67 22 100 11 11 

FVIII indicates factor VIII; and ITI, immune tolerance induction therapy.

*

Many samples contained different populations of antibodies that were individually assessed for prevalence. Therefore, the sum of the prevalence of the individual isotypes and subclasses may be > 100%.

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