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. 2017 May 15;130(6):808–816. doi: 10.1182/blood-2016-11-751347

Table 1.

Frequency of fVIII domain-specific antibodies in acquired and congenital hemophilia inhibitor patients

Study Number of patients Absolute and relative number of patients with IgG binding to
HSA-domain fusion proteins SHD hpfVIII proteins
A2 C1 C2 A2 C1 C2
AHA group I, n (%) 23 4 (17) 12 (52) 17 (74) 1 (4) 5 (22) 12 (52)
AHA group II, n (%) 92 23 (25) 78 (85) 61 (66) 20 (22) 29 (32) 49 (53)
Total AHA, n (%) 115 27 (23) 90 (78) 78 (68) 21 (18) 34 (30) 61 (53)
HA group I, n (%) 33 28 (85) 23 (70) 31 (94) 13 (39) 4 (12) 18 (55)
HA group II, n (%) 30 5 (17) 13 (43) 20 (67) 5 (17) 0 (0) 14 (47)
Total HA, n (%) 63 33 (52) 36 (57) 51 (81) 18 (29) 4 (6) 32 (51)
AHA + HA, n (%) 178 60 (34) 126 (71) 129 (72) 39 (22) 38 (21) 93 (52)

The frequency of fVIII domain-specific IgG in patients with AHA and congenital HA and inhibitors to human A2, C1, or C2 domains was measured by ELISA using HSA-fVIII domain fusion proteins and SHD hpfVIII proteins as antigens. For details regarding patient groups and experimental settings, see “Methods”.