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Detection of anti-desmoglein antibodies in oral lichen planus: What do we know so far

Oral lichen planus (OLP) is an inflammatory disease of the oral mucosa. Clinically, two main subsets are described, namely non-erosive and erosive OLP. While non-erosive OLP is usually responsive to local therapies, erosive OLP is often refractory also to systemic therapies and extremely reduces the...

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Autores principales: Didona, Dario, Hertl, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575987/
https://www.ncbi.nlm.nih.gov/pubmed/36263026
http://dx.doi.org/10.3389/fimmu.2022.1001970
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author Didona, Dario
Hertl, Michael
author_facet Didona, Dario
Hertl, Michael
author_sort Didona, Dario
collection PubMed
description Oral lichen planus (OLP) is an inflammatory disease of the oral mucosa. Clinically, two main subsets are described, namely non-erosive and erosive OLP. While non-erosive OLP is usually responsive to local therapies, erosive OLP is often refractory also to systemic therapies and extremely reduces the quality of life of the patients. Furthermore, in some erosive OLP cases different autoantibodies have been detected, including anti-desmoglein 1 and 3 autoantibodies, and anti-bullous pemphigoid 180 and 230 autoantibodies. However, their potential role is still not clear. In this paper, we reviewed the literature about the detection of autoantibodies against desmoglein 1 and 3, the main target antigens of pemphigus vulgaris, in patient with OLP, summarizing the more recent insights on this topic.
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spelling pubmed-95759872022-10-18 Detection of anti-desmoglein antibodies in oral lichen planus: What do we know so far Didona, Dario Hertl, Michael Front Immunol Immunology Oral lichen planus (OLP) is an inflammatory disease of the oral mucosa. Clinically, two main subsets are described, namely non-erosive and erosive OLP. While non-erosive OLP is usually responsive to local therapies, erosive OLP is often refractory also to systemic therapies and extremely reduces the quality of life of the patients. Furthermore, in some erosive OLP cases different autoantibodies have been detected, including anti-desmoglein 1 and 3 autoantibodies, and anti-bullous pemphigoid 180 and 230 autoantibodies. However, their potential role is still not clear. In this paper, we reviewed the literature about the detection of autoantibodies against desmoglein 1 and 3, the main target antigens of pemphigus vulgaris, in patient with OLP, summarizing the more recent insights on this topic. Frontiers Media S.A. 2022-10-03 /pmc/articles/PMC9575987/ /pubmed/36263026 http://dx.doi.org/10.3389/fimmu.2022.1001970 Text en Copyright © 2022 Didona and Hertl https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Didona, Dario
Hertl, Michael
Detection of anti-desmoglein antibodies in oral lichen planus: What do we know so far
title Detection of anti-desmoglein antibodies in oral lichen planus: What do we know so far
title_full Detection of anti-desmoglein antibodies in oral lichen planus: What do we know so far
title_fullStr Detection of anti-desmoglein antibodies in oral lichen planus: What do we know so far
title_full_unstemmed Detection of anti-desmoglein antibodies in oral lichen planus: What do we know so far
title_short Detection of anti-desmoglein antibodies in oral lichen planus: What do we know so far
title_sort detection of anti-desmoglein antibodies in oral lichen planus: what do we know so far
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575987/
https://www.ncbi.nlm.nih.gov/pubmed/36263026
http://dx.doi.org/10.3389/fimmu.2022.1001970
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