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Molecular diagnosis of anti-laminin 332 (epiligrin) mucous membrane pemphigoid

BACKGROUND: Mucous membrane pemphigoid is a group of chronic subepithelial autoimmune blistering diseases that mainly affect mucous membranes. Laminin 332-specific autoantibodies are present in approximately 1/3 of the patients, being associated with an increased risk of malignancy. Because of the s...

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Autores principales: Chiorean, Roxana, Danescu, Sorina, Virtic, Oana, Mustafa, Mayson B., Baican, Adrian, Lischka, Annette, Hashimoto, Takashi, Kariya, Yoshinobu, Koch, Manuel, Sitaru, Cassian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6035451/
https://www.ncbi.nlm.nih.gov/pubmed/29980216
http://dx.doi.org/10.1186/s13023-018-0855-x
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author Chiorean, Roxana
Danescu, Sorina
Virtic, Oana
Mustafa, Mayson B.
Baican, Adrian
Lischka, Annette
Hashimoto, Takashi
Kariya, Yoshinobu
Koch, Manuel
Sitaru, Cassian
author_facet Chiorean, Roxana
Danescu, Sorina
Virtic, Oana
Mustafa, Mayson B.
Baican, Adrian
Lischka, Annette
Hashimoto, Takashi
Kariya, Yoshinobu
Koch, Manuel
Sitaru, Cassian
author_sort Chiorean, Roxana
collection PubMed
description BACKGROUND: Mucous membrane pemphigoid is a group of chronic subepithelial autoimmune blistering diseases that mainly affect mucous membranes. Laminin 332-specific autoantibodies are present in approximately 1/3 of the patients, being associated with an increased risk of malignancy. Because of the severe complications, an early recognition of the disease allowing a timely therapy is essential. The gold standard methods for detection of laminin 332-specific autoantibodies, including the immunoprecipitation and immunoblotting are non-quantitative, laborious and restricted to a few specialized laboratories worldwide. In addition, the use of radioimmunoassays, although highly sensitive and specific, are laborious, expensive and tightly regulated. Therefore, there is a stringent need for a quantitative immunoassay for the routine detection of laminin 332-specific autoantibodies more broadly available to diagnostic laboratories. The aim of this study was to compare different antigenic substrates, including native, recombinant laminin 332 and laminin 332-rich keratinocyte extracellular matrix, for development of an ELISA to detect autoantibodies in mucous membrane pemphigoid. RESULTS: Using a relatively large number of sera from MMP patients with well-characterized autoantibody reactivity we show the suitability of ELISA systems using laminin 332 preparations as adjunct diagnostic tools in MMP. While glycosylation of laminin 332 does not appear to influence its recognition by MMP autoantibodies, ELISA systems using both purified, native and recombinant laminin 332 demonstrated a high sensitivity and good correlation with the detection of autoantibodies by immunoblotting. ELISA systems using different laminin 332 preparations represent a feasible and more accessible alternative for a broad range of laboratories. CONCLUSIONS: Our findings qualify the use of immunoassays with the laminin 332-rich preparations as an ancillary diagnostic tool in mucous membrane pemphigoid. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13023-018-0855-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-60354512018-07-09 Molecular diagnosis of anti-laminin 332 (epiligrin) mucous membrane pemphigoid Chiorean, Roxana Danescu, Sorina Virtic, Oana Mustafa, Mayson B. Baican, Adrian Lischka, Annette Hashimoto, Takashi Kariya, Yoshinobu Koch, Manuel Sitaru, Cassian Orphanet J Rare Dis Research BACKGROUND: Mucous membrane pemphigoid is a group of chronic subepithelial autoimmune blistering diseases that mainly affect mucous membranes. Laminin 332-specific autoantibodies are present in approximately 1/3 of the patients, being associated with an increased risk of malignancy. Because of the severe complications, an early recognition of the disease allowing a timely therapy is essential. The gold standard methods for detection of laminin 332-specific autoantibodies, including the immunoprecipitation and immunoblotting are non-quantitative, laborious and restricted to a few specialized laboratories worldwide. In addition, the use of radioimmunoassays, although highly sensitive and specific, are laborious, expensive and tightly regulated. Therefore, there is a stringent need for a quantitative immunoassay for the routine detection of laminin 332-specific autoantibodies more broadly available to diagnostic laboratories. The aim of this study was to compare different antigenic substrates, including native, recombinant laminin 332 and laminin 332-rich keratinocyte extracellular matrix, for development of an ELISA to detect autoantibodies in mucous membrane pemphigoid. RESULTS: Using a relatively large number of sera from MMP patients with well-characterized autoantibody reactivity we show the suitability of ELISA systems using laminin 332 preparations as adjunct diagnostic tools in MMP. While glycosylation of laminin 332 does not appear to influence its recognition by MMP autoantibodies, ELISA systems using both purified, native and recombinant laminin 332 demonstrated a high sensitivity and good correlation with the detection of autoantibodies by immunoblotting. ELISA systems using different laminin 332 preparations represent a feasible and more accessible alternative for a broad range of laboratories. CONCLUSIONS: Our findings qualify the use of immunoassays with the laminin 332-rich preparations as an ancillary diagnostic tool in mucous membrane pemphigoid. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13023-018-0855-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-06 /pmc/articles/PMC6035451/ /pubmed/29980216 http://dx.doi.org/10.1186/s13023-018-0855-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Chiorean, Roxana
Danescu, Sorina
Virtic, Oana
Mustafa, Mayson B.
Baican, Adrian
Lischka, Annette
Hashimoto, Takashi
Kariya, Yoshinobu
Koch, Manuel
Sitaru, Cassian
Molecular diagnosis of anti-laminin 332 (epiligrin) mucous membrane pemphigoid
title Molecular diagnosis of anti-laminin 332 (epiligrin) mucous membrane pemphigoid
title_full Molecular diagnosis of anti-laminin 332 (epiligrin) mucous membrane pemphigoid
title_fullStr Molecular diagnosis of anti-laminin 332 (epiligrin) mucous membrane pemphigoid
title_full_unstemmed Molecular diagnosis of anti-laminin 332 (epiligrin) mucous membrane pemphigoid
title_short Molecular diagnosis of anti-laminin 332 (epiligrin) mucous membrane pemphigoid
title_sort molecular diagnosis of anti-laminin 332 (epiligrin) mucous membrane pemphigoid
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6035451/
https://www.ncbi.nlm.nih.gov/pubmed/29980216
http://dx.doi.org/10.1186/s13023-018-0855-x
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