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Cytokines Levels and Salivary Microbiome Play A Potential Role in Oral Lichen Planus Diagnosis

Oral lichen planus (OLP) is a chronic Th1-mediated inflammatory mucocutaneous disease of the skin and oral mucosa that can have various clinical presentations. Lesions are usually bilateral and often painful. While cutaneous Lichen Planus (LP) lesions are self-limiting, the oral lesions are chronic...

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Autores principales: Carvalho, Maria Fernanda Marques Silva de, Cavalieri, Denise, Do Nascimento, Sabrina, Lourenço, Talita Gomes Baeta, Ramos, Danielle Viana Ribeiro, Pasqualin, Denise da Cunha, Martins, Leandro Aurélio Liporoni, Rocha, Fernanda Agostini, Heller, Débora, Marti, Luciana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889227/
https://www.ncbi.nlm.nih.gov/pubmed/31792433
http://dx.doi.org/10.1038/s41598-019-54615-y
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author Carvalho, Maria Fernanda Marques Silva de
Cavalieri, Denise
Do Nascimento, Sabrina
Lourenço, Talita Gomes Baeta
Ramos, Danielle Viana Ribeiro
Pasqualin, Denise da Cunha
Martins, Leandro Aurélio Liporoni
Rocha, Fernanda Agostini
Heller, Débora
Marti, Luciana
author_facet Carvalho, Maria Fernanda Marques Silva de
Cavalieri, Denise
Do Nascimento, Sabrina
Lourenço, Talita Gomes Baeta
Ramos, Danielle Viana Ribeiro
Pasqualin, Denise da Cunha
Martins, Leandro Aurélio Liporoni
Rocha, Fernanda Agostini
Heller, Débora
Marti, Luciana
author_sort Carvalho, Maria Fernanda Marques Silva de
collection PubMed
description Oral lichen planus (OLP) is a chronic Th1-mediated inflammatory mucocutaneous disease of the skin and oral mucosa that can have various clinical presentations. Lesions are usually bilateral and often painful. While cutaneous Lichen Planus (LP) lesions are self-limiting, the oral lesions are chronic and rarely remissive. The diagnosis of oral lichen planus (OLP) is often challenging, and confirmation by histopathological criterion is generally advised. The aim of our study was to identify the cytokines present in OLP-suggestive lesions and in non-specific inflammatory lesions (NSIL) used as controls. Moreover, assess cytokines protein levels and oral microbiota composition in whole saliva samples. Histopathological analysis, immunohistochemistry and gene expression were used as techniques to analyze the oral mucosal tissue samples. ELISA was conducted to analyze salivary cytokine levels and 16S rRNA sequencing was used to determine the salivary microbiome. As a result we observed larger number of infiltrated lymphocytes (p = 0.025), as well, more T CD4 lymphocytes in the epithelial tissue (p = 0.006) in OLP samples compared to NSIL. In addition, the OLP samples displayed more apoptotic cells compared to NSIL (p = 0.047). Regarding the cytokine analysis, IFN-γ and IL-33 were more expressed in OLP lesions than in NSIL samples (p < 0.001; p = 0.026). Furthermore, our results demonstrated higher levels of IFN-γ protein expression in the saliva of OLP group compared to controls (p = 0.0156). We also observed noted differences in the oral microbiota composition between OLP and NSIL saliva samples. In conclusion, OLP lesions presented larger numbers of apoptotic and inflammatory cells, higher levels of IFN-γ and IL-33 compared to NSIL, and these lesions also differ regarding oral microbiota composition. These results are consistent with the Th-1-mediated chronic inflammation nature of oral lichen planus investigated lesions and displayed unique features that could be used as a diagnostic tool.
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spelling pubmed-68892272019-12-10 Cytokines Levels and Salivary Microbiome Play A Potential Role in Oral Lichen Planus Diagnosis Carvalho, Maria Fernanda Marques Silva de Cavalieri, Denise Do Nascimento, Sabrina Lourenço, Talita Gomes Baeta Ramos, Danielle Viana Ribeiro Pasqualin, Denise da Cunha Martins, Leandro Aurélio Liporoni Rocha, Fernanda Agostini Heller, Débora Marti, Luciana Sci Rep Article Oral lichen planus (OLP) is a chronic Th1-mediated inflammatory mucocutaneous disease of the skin and oral mucosa that can have various clinical presentations. Lesions are usually bilateral and often painful. While cutaneous Lichen Planus (LP) lesions are self-limiting, the oral lesions are chronic and rarely remissive. The diagnosis of oral lichen planus (OLP) is often challenging, and confirmation by histopathological criterion is generally advised. The aim of our study was to identify the cytokines present in OLP-suggestive lesions and in non-specific inflammatory lesions (NSIL) used as controls. Moreover, assess cytokines protein levels and oral microbiota composition in whole saliva samples. Histopathological analysis, immunohistochemistry and gene expression were used as techniques to analyze the oral mucosal tissue samples. ELISA was conducted to analyze salivary cytokine levels and 16S rRNA sequencing was used to determine the salivary microbiome. As a result we observed larger number of infiltrated lymphocytes (p = 0.025), as well, more T CD4 lymphocytes in the epithelial tissue (p = 0.006) in OLP samples compared to NSIL. In addition, the OLP samples displayed more apoptotic cells compared to NSIL (p = 0.047). Regarding the cytokine analysis, IFN-γ and IL-33 were more expressed in OLP lesions than in NSIL samples (p < 0.001; p = 0.026). Furthermore, our results demonstrated higher levels of IFN-γ protein expression in the saliva of OLP group compared to controls (p = 0.0156). We also observed noted differences in the oral microbiota composition between OLP and NSIL saliva samples. In conclusion, OLP lesions presented larger numbers of apoptotic and inflammatory cells, higher levels of IFN-γ and IL-33 compared to NSIL, and these lesions also differ regarding oral microbiota composition. These results are consistent with the Th-1-mediated chronic inflammation nature of oral lichen planus investigated lesions and displayed unique features that could be used as a diagnostic tool. Nature Publishing Group UK 2019-12-02 /pmc/articles/PMC6889227/ /pubmed/31792433 http://dx.doi.org/10.1038/s41598-019-54615-y Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Carvalho, Maria Fernanda Marques Silva de
Cavalieri, Denise
Do Nascimento, Sabrina
Lourenço, Talita Gomes Baeta
Ramos, Danielle Viana Ribeiro
Pasqualin, Denise da Cunha
Martins, Leandro Aurélio Liporoni
Rocha, Fernanda Agostini
Heller, Débora
Marti, Luciana
Cytokines Levels and Salivary Microbiome Play A Potential Role in Oral Lichen Planus Diagnosis
title Cytokines Levels and Salivary Microbiome Play A Potential Role in Oral Lichen Planus Diagnosis
title_full Cytokines Levels and Salivary Microbiome Play A Potential Role in Oral Lichen Planus Diagnosis
title_fullStr Cytokines Levels and Salivary Microbiome Play A Potential Role in Oral Lichen Planus Diagnosis
title_full_unstemmed Cytokines Levels and Salivary Microbiome Play A Potential Role in Oral Lichen Planus Diagnosis
title_short Cytokines Levels and Salivary Microbiome Play A Potential Role in Oral Lichen Planus Diagnosis
title_sort cytokines levels and salivary microbiome play a potential role in oral lichen planus diagnosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889227/
https://www.ncbi.nlm.nih.gov/pubmed/31792433
http://dx.doi.org/10.1038/s41598-019-54615-y
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