Detection of adrenocortical autoantibodies in Addison's disease with a peroxidase-labelled protein A technique

Adrenocortical autoantibodies (ACA), present in 60-80% of patients with idiopathic Addison's disease, are conventionally detected by indirect immunofluorescence (IIF) on frozen sections of adrenal glands. The large-scale use of IIF is limited in part by the need for a fluorescence microscope an...

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Main Authors: R.C. Silva, S. Faiçal, S. Laureti, A. Falorni, S.A. Dib, C.E. Kater
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 1998-09-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1998000900007
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author R.C. Silva
S. Faiçal
S. Laureti
A. Falorni
S.A. Dib
C.E. Kater
author_facet R.C. Silva
S. Faiçal
S. Laureti
A. Falorni
S.A. Dib
C.E. Kater
author_sort R.C. Silva
collection DOAJ
description Adrenocortical autoantibodies (ACA), present in 60-80% of patients with idiopathic Addison's disease, are conventionally detected by indirect immunofluorescence (IIF) on frozen sections of adrenal glands. The large-scale use of IIF is limited in part by the need for a fluorescence microscope and the fact that histological sections cannot be stored for long periods of time. To circumvent these restrictions we developed a novel peroxidase-labelled protein A (PLPA) technique for the detection of ACA in patients with Addison's disease and compared the results with those obtained with the classical IIF assay. We studied serum samples from 90 healthy control subjects and 22 patients with Addison's disease, who had been clinically classified into two groups: idiopathic (N = 13) and granulomatous (N = 9). ACA-PLPA were detected in 10/22 (45%) patients: 9/13 (69%) with the idiopathic form and 1/9 (11%) with the granulomatous form, whereas ACA-IIF were detected in 11/22 patients (50%): 10/13 (77%) with the idiopathic form and 1/9 (11%) with the granulomatous form. Twelve of the 13 idiopathic addisonians (92%) were positive for either ACA-PLPA or ACA-IIF, but only 7 were positive by both methods. In contrast, none of 90 healthy subjects was found to be positive for ACA. Thus, our study shows that the PLPA-based technique is useful, has technical advantages over the IIF method (by not requiring the use of a fluorescence microscope and by permitting section storage for long periods of time). However, since it is only 60% concordant with the ACA-IIF method, it should be considered complementary instead of an alternative method to IIF for the detection of ACA in human sera.
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spelling doaj.art-07e40e805eb74b2eb527652e53cce1f42022-12-22T01:58:10ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research0100-879X1414-431X1998-09-01319114110.1590/S0100-879X1998000900007Detection of adrenocortical autoantibodies in Addison's disease with a peroxidase-labelled protein A techniqueR.C. SilvaS. FaiçalS. LauretiA. FalorniS.A. DibC.E. KaterAdrenocortical autoantibodies (ACA), present in 60-80% of patients with idiopathic Addison's disease, are conventionally detected by indirect immunofluorescence (IIF) on frozen sections of adrenal glands. The large-scale use of IIF is limited in part by the need for a fluorescence microscope and the fact that histological sections cannot be stored for long periods of time. To circumvent these restrictions we developed a novel peroxidase-labelled protein A (PLPA) technique for the detection of ACA in patients with Addison's disease and compared the results with those obtained with the classical IIF assay. We studied serum samples from 90 healthy control subjects and 22 patients with Addison's disease, who had been clinically classified into two groups: idiopathic (N = 13) and granulomatous (N = 9). ACA-PLPA were detected in 10/22 (45%) patients: 9/13 (69%) with the idiopathic form and 1/9 (11%) with the granulomatous form, whereas ACA-IIF were detected in 11/22 patients (50%): 10/13 (77%) with the idiopathic form and 1/9 (11%) with the granulomatous form. Twelve of the 13 idiopathic addisonians (92%) were positive for either ACA-PLPA or ACA-IIF, but only 7 were positive by both methods. In contrast, none of 90 healthy subjects was found to be positive for ACA. Thus, our study shows that the PLPA-based technique is useful, has technical advantages over the IIF method (by not requiring the use of a fluorescence microscope and by permitting section storage for long periods of time). However, since it is only 60% concordant with the ACA-IIF method, it should be considered complementary instead of an alternative method to IIF for the detection of ACA in human sera.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1998000900007autoantibodies detectionAddison's diseaseperoxidase-labelled protein Aindirect immunofluorescenceadrenal gland
spellingShingle R.C. Silva
S. Faiçal
S. Laureti
A. Falorni
S.A. Dib
C.E. Kater
Detection of adrenocortical autoantibodies in Addison's disease with a peroxidase-labelled protein A technique
Brazilian Journal of Medical and Biological Research
autoantibodies detection
Addison's disease
peroxidase-labelled protein A
indirect immunofluorescence
adrenal gland
title Detection of adrenocortical autoantibodies in Addison's disease with a peroxidase-labelled protein A technique
title_full Detection of adrenocortical autoantibodies in Addison's disease with a peroxidase-labelled protein A technique
title_fullStr Detection of adrenocortical autoantibodies in Addison's disease with a peroxidase-labelled protein A technique
title_full_unstemmed Detection of adrenocortical autoantibodies in Addison's disease with a peroxidase-labelled protein A technique
title_short Detection of adrenocortical autoantibodies in Addison's disease with a peroxidase-labelled protein A technique
title_sort detection of adrenocortical autoantibodies in addison s disease with a peroxidase labelled protein a technique
topic autoantibodies detection
Addison's disease
peroxidase-labelled protein A
indirect immunofluorescence
adrenal gland
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1998000900007
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