Vitiligo is considered an autoimmune disorder due to the generation an
d presence of autoantibodies directed against melanocyte antigens in t
he patients' sera. In the present study we point towards a newly defin
ed autoantigen in vitiligo, the enzyme tyrosinase, which participates
in the process oi. melanogenesis. Anti-tyrosinase antibodies were dete
cted in the sera of seven patients with diffuse and 11 patients with l
ocalized vitiligo. Employing solid-phase ELISA to mushroom tyrosinase,
we found that patients with diffuse vitiligo had significantly higher
titres of IgG anti-tyrosinase autoantibodies than patients with local
ized disease or healthy subjects. These anti-tyrosinase autoantibodies
have relatively high functional affinity to tyrosinase and can be rec
overed from vitiligo patients' sera by affinity purification. The anti
-tyrosinase antibodies do not cross-react with other enzymes recognize
d as autoantigens in different autoimmune disorders and the autoantibo
dies do not block the enzymatic activity of tyrosinase, indicating tha
t they are not reacting with the catalytic site of the enzyme. These d
ata point to tyrosinase as an autoantigen in vitiligo and suggest that
anti-tyrosinase titres call serve as a marker for disease activity.