Transgenic non obese diabetic mice (NOD) have been generated that expr
ess murine heat shock protein 60 (Hsp60) on an H-2E alpha promoter. Th
ese mice have been shown to be protected from diabetes, but to suffer
from exacerbated sialitis and experimental autoimmune encephalomyeliti
s (EAE). Protection from diabetes is not the result of negative select
ion of all Hsp60 reactive T cell clones; responses to self Hsp60 are o
bserved despite high expression in the thymus [1].