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TOLL-LIKE RECEPTORS (TLR) 2 AND 4 EXPRESSION OF KERATINOCYTES FROM PATIENTS WITH LOCALIZED AND DISSEMINATED DERMATOPHYTOSIS
There are few studies on the role of innate immune response in dermatophytosis. An investigation was conducted to define the involvement of Toll-Like Receptors (TLRs) 2 and 4 in localized (LD) and disseminated (DD) dermatophytosis due to T. rubrum. Fifteen newly diagnosed patients, eight patients wi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Instituto de Medicina Tropical
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4325524/ https://www.ncbi.nlm.nih.gov/pubmed/25651327 http://dx.doi.org/10.1590/S0036-46652015000100008 |
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author | de Oliveira, Cristiane Beatriz Vasconcellos, Cídia Sakai-Valente, Neusa Y. Sotto, Mirian Nacagami Luiz, Fernanda Guedes Belda, Walter de Sousa, Maria da Gloria Teixeira Benard, Gil Criado, Paulo Ricardo |
author_facet | de Oliveira, Cristiane Beatriz Vasconcellos, Cídia Sakai-Valente, Neusa Y. Sotto, Mirian Nacagami Luiz, Fernanda Guedes Belda, Walter de Sousa, Maria da Gloria Teixeira Benard, Gil Criado, Paulo Ricardo |
author_sort | de Oliveira, Cristiane Beatriz |
collection | PubMed |
description | There are few studies on the role of innate immune response in dermatophytosis. An investigation was conducted to define the involvement of Toll-Like Receptors (TLRs) 2 and 4 in localized (LD) and disseminated (DD) dermatophytosis due to T. rubrum. Fifteen newly diagnosed patients, eight patients with LD and seven with DD, defined by involvement of at least three body segments were used in this study. Controls comprised twenty skin samples from healthy individuals undergoing plastic surgery. TLR2 and TLR4 were quantified in skin lesions by immunohistochemistry. A reduced expression of TLR4 in the lower and upper epidermis of both LD and DD patients was found compared to controls; TLR2 expression was preserved in the upper and lower epidermis of all three groups. As TLR4 signaling induces the production of inflammatory cytokines and neutrophils recruitment, its reduced expression likely contributed to the lack of resolution of the infection and the consequent chronic nature of the dermatophytosis. As TLR2 expression acts to limit the inflammatory process and preserves the epidermal structure, its preserved expression may also contribute to the persistent infection and limited inflammation that are characteristic of dermatophytic infections. |
format | Online Article Text |
id | pubmed-4325524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Instituto de Medicina Tropical |
record_format | MEDLINE/PubMed |
spelling | pubmed-43255242015-02-13 TOLL-LIKE RECEPTORS (TLR) 2 AND 4 EXPRESSION OF KERATINOCYTES FROM PATIENTS WITH LOCALIZED AND DISSEMINATED DERMATOPHYTOSIS de Oliveira, Cristiane Beatriz Vasconcellos, Cídia Sakai-Valente, Neusa Y. Sotto, Mirian Nacagami Luiz, Fernanda Guedes Belda, Walter de Sousa, Maria da Gloria Teixeira Benard, Gil Criado, Paulo Ricardo Rev Inst Med Trop Sao Paulo Mycology There are few studies on the role of innate immune response in dermatophytosis. An investigation was conducted to define the involvement of Toll-Like Receptors (TLRs) 2 and 4 in localized (LD) and disseminated (DD) dermatophytosis due to T. rubrum. Fifteen newly diagnosed patients, eight patients with LD and seven with DD, defined by involvement of at least three body segments were used in this study. Controls comprised twenty skin samples from healthy individuals undergoing plastic surgery. TLR2 and TLR4 were quantified in skin lesions by immunohistochemistry. A reduced expression of TLR4 in the lower and upper epidermis of both LD and DD patients was found compared to controls; TLR2 expression was preserved in the upper and lower epidermis of all three groups. As TLR4 signaling induces the production of inflammatory cytokines and neutrophils recruitment, its reduced expression likely contributed to the lack of resolution of the infection and the consequent chronic nature of the dermatophytosis. As TLR2 expression acts to limit the inflammatory process and preserves the epidermal structure, its preserved expression may also contribute to the persistent infection and limited inflammation that are characteristic of dermatophytic infections. Instituto de Medicina Tropical 2015 /pmc/articles/PMC4325524/ /pubmed/25651327 http://dx.doi.org/10.1590/S0036-46652015000100008 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Mycology de Oliveira, Cristiane Beatriz Vasconcellos, Cídia Sakai-Valente, Neusa Y. Sotto, Mirian Nacagami Luiz, Fernanda Guedes Belda, Walter de Sousa, Maria da Gloria Teixeira Benard, Gil Criado, Paulo Ricardo TOLL-LIKE RECEPTORS (TLR) 2 AND 4 EXPRESSION OF KERATINOCYTES FROM PATIENTS WITH LOCALIZED AND DISSEMINATED DERMATOPHYTOSIS |
title | TOLL-LIKE RECEPTORS (TLR) 2 AND 4 EXPRESSION OF KERATINOCYTES FROM
PATIENTS WITH LOCALIZED AND DISSEMINATED DERMATOPHYTOSIS |
title_full | TOLL-LIKE RECEPTORS (TLR) 2 AND 4 EXPRESSION OF KERATINOCYTES FROM
PATIENTS WITH LOCALIZED AND DISSEMINATED DERMATOPHYTOSIS |
title_fullStr | TOLL-LIKE RECEPTORS (TLR) 2 AND 4 EXPRESSION OF KERATINOCYTES FROM
PATIENTS WITH LOCALIZED AND DISSEMINATED DERMATOPHYTOSIS |
title_full_unstemmed | TOLL-LIKE RECEPTORS (TLR) 2 AND 4 EXPRESSION OF KERATINOCYTES FROM
PATIENTS WITH LOCALIZED AND DISSEMINATED DERMATOPHYTOSIS |
title_short | TOLL-LIKE RECEPTORS (TLR) 2 AND 4 EXPRESSION OF KERATINOCYTES FROM
PATIENTS WITH LOCALIZED AND DISSEMINATED DERMATOPHYTOSIS |
title_sort | toll-like receptors (tlr) 2 and 4 expression of keratinocytes from
patients with localized and disseminated dermatophytosis |
topic | Mycology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4325524/ https://www.ncbi.nlm.nih.gov/pubmed/25651327 http://dx.doi.org/10.1590/S0036-46652015000100008 |
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