Table 1.
IgG | Treatment | Oligosaccharide specificity | # mice tested | # mice with skin blister | # mice without skin blister |
---|---|---|---|---|---|
PF-1 | Vehicle | 15 | 15 | 0 | |
Jacalin | Galβ1-3GalNAc-α (asialo or sialo) | 8 | 0 | 8 | |
PNA | GalNAc Galβ1-3GalNAc-α or -β (asialo) | 9 | 1* | 8 | |
VVL-B4 | GalNAc | 3 | 3 | 0 | |
PF-2 | Vehicle | 6 | 6 | 0 | |
Jacalin | 6 | 5** | 1 |
Neonatal mice were preinjected (s.c.) with vehicle (TBS-Ca2+) or lectins for 2 h followed by pathogenic PF IgG injection (s.c.). Pathogenic IgG from two patients’ sera was used. PF-1 serum showed a remarkable inhibition in Dsgl binding by jacalin, whereas PF-2 showed a marginal reduction in Dsgl binding by jacalin. Animals were evaluated 20 h post PF IgG injection. Jacalin: 80 to 160 μg/g b.w.; PNA and VVL-B4: 160 μg/g b.w. Abbreviations: Gal, galactose; GalNAc, N-acetylglactosamine; Glc, glucose; PNA, peanut agglutinin; VVL-B4, vicia villosa-B4 lectin.
Minimum disease score (0.5+).
Overall less disease score (1.25 + 0.36) compared to those preinjected with vehicle (2.58 + 0.20) (p<0.01, Students’ t-test).