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. Author manuscript; available in PMC: 2011 Dec 1.
Published in final edited form as: J Invest Dermatol. 2010 Jul 15;130(12):2773–2780. doi: 10.1038/jid.2010.209

Table 1.

In vivo effect of plant lectins in IgG passive transfer mouse model of PF

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).