Adrenal-cortex autoantibodies and steroid-producing cells autoantibodies in patients with Addison's disease: Comparison of immunofluorescence and immunoprecipitation assays
C. Betterle et al., Adrenal-cortex autoantibodies and steroid-producing cells autoantibodies in patients with Addison's disease: Comparison of immunofluorescence and immunoprecipitation assays, J CLIN END, 84(2), 1999, pp. 618-622
Autoimmune Addison's disease and premature ovarian failure are characterize
d by the presence of organ-specific autoantibodies. The main adrenal and go
nadal autoantigens have been identified and cloned, and the relationship be
tween the autoantibodies detected by immunofluorescence techniques and thos
e detected by the new assays using recombinant autoantigens needed to be in
vestigated. We studied 165 patients with Addison's disease: 143 patients ha
d different forms of autoimmune Addison's disease (13 with idiopathic prema
ture ovarian failure) and 22 had nonautoimmune Addison's disease. Adrenal-c
ortex autoantibodies and steroid-producing cell autoantibodies were measure
d by the immunofluorescence techniques. Autoantibodies to steroid 21-hydrox
ylase, 17 alpha-hydroxylase, and P450 side chain cleavage enzyme were measu
red by immunoprecipitation assay using S-35-labeled recombinant proteins.
Adrenal-cortex autoantibodies and autoantibodies to 21-hydroxylase were fou
nd in 81% of the patients with autoimmune Addison's disease. None of the pa
tients with nonautoimmune Addison's disease had adrenal-cortex autoantibodi
es or autoantibodies to 21-hydroxylase. A high association between these tw
o markers in patients with different forms of autoimmune Addison's disease
and in those with short- or long-standing disease was found. Steroid-produc
ing cells autoantibodies were found in 26% of the patients with autoimmune
Addison's disease, and autoantibodies to 17 alpha-hydroxylase and/or P450 s
ide chain cleavage enzyme in 36% of the patients. Steroid-producing cells a
utoantibodies were found in 11/13 (85%) of patients with idiopathic prematu
re ovarian failure associated with autoimmune Addison's disease, and autoan
tibodies to 17 alpha-hydroxylase and/or P450 side chain cleavage were found
12/13 (92%) of patients; the only case negative for all these three marker
s suffered from Turner's syndrome.
Provided that a high standard of immunofluorescence technique is maintained
, measurement of adrenal cortex autoantibodies or steroid-producing cells a
utoantibodies by either immunofluorescence or immunoprecipitation assay is
essentially equivalent.