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. Author manuscript; available in PMC: 2010 Jan 1.
Published in final edited form as: J Immunol. 2009 Jan 1;182(1):711–717. doi: 10.4049/jimmunol.182.1.711

Table I.

Blockade of experimental PF by the caspase inhibitors*

IgG injected Treatment # of mice Disease Score
(Mean ± SD)
PF1 Vehicle 8 2.5 ± 0.3
Ac-DEVD-cmk 6 0
Boc-D-fmk 3 0
PF2 Vehicle 6 2.3 ± 0.3
Ac-DEVD-cmk 3 0
Boc-D-fmk 3 0
*

Neonatal mice were preinjected (s.c.) with the caspase inhibitor or control vehicle. One and a half hour later, mice were injected (s.c.) with the pathogenic IgG prepared from two PF patients (PF1 and PF2) along with the inhibitor or vehicl. The total doses for Ac-DEVD-cmk were 3.4 or 6.8 µg/g b.w. and for Boc-D-fmk was 6.8 µg/g b.w. Injected animals were examined clinically 20 h after IgG injection, and clinical disease was scored. There is a significant difference in clinical disease scores between mice treated with vehicle and mice treated with Ac-DEVD-cmk or Boc-D-fmk (p < 0.0001, Student’s t test).