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T regulatory cells (TREG)(TCD4+CD25+FOXP3+) distribution in the different clinical forms of leprosy and reactional states()
BACKGROUND: Leprosy is characterized histologically by a spectrum of different granulomatous skin lesions, reflecting patients' immune responses to Mycobacterium leprae. Although CD4+CD25+ FoxP3+ T regulatory cells are pivotal in the immuneregulation, presence, frequency, and distribution of Tr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Dermatologia
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323697/ https://www.ncbi.nlm.nih.gov/pubmed/25672298 http://dx.doi.org/10.1590/abd1806-4841.20153311 |
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author | Parente, José Napoleão Tavares Talhari, Carolina Schettini, Antônio Pedro Mendes Massone, Cesare |
author_facet | Parente, José Napoleão Tavares Talhari, Carolina Schettini, Antônio Pedro Mendes Massone, Cesare |
author_sort | Parente, José Napoleão Tavares |
collection | PubMed |
description | BACKGROUND: Leprosy is characterized histologically by a spectrum of different granulomatous skin lesions, reflecting patients' immune responses to Mycobacterium leprae. Although CD4+CD25+ FoxP3+ T regulatory cells are pivotal in the immuneregulation, presence, frequency, and distribution of Tregs in leprosy, its reactional states have been investigated in few studies. OBJECTIVES: This study aimed to verify the frequency and distribution of regulatory T cells in different clinical forms and reactional states of leprosy. METHODS: We performed an immunohistochemical study on 96 leprosy cases [Indeterminate (I): 9 patients; tuberculoid tuberculoid: 13 patients; borderline tuberculoid: 26 patients; borderline borderline: 3 patients; borderline lepromatous: 8 patients; lepromatous lepromatous: 27 patients; reversal reaction: 8 patients; and erythema nodosum leprosum: 2 patients]. RESULTS: FoxP3-positive cells were present in 100% of the cases with an average density of 2.82% of the infiltrate. Their distribution was not related to granulomatous structures or special locations. There was a statistically significant increment of FoxP3 expression in patients with leprosy reversal reactions when compared with patients presenting with type I leprosy (P= 0.0228); borderline tuberculoid leprosy (P = 0.0351) and lepromatous leprosy (P = 0.0344). CONCLUSIONS: These findings suggest that Tregs play a relevant role in the etiopathogenesis of leprosy, mainly in type I leprosy reaction. |
format | Online Article Text |
id | pubmed-4323697 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Sociedade Brasileira de Dermatologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-43236972015-02-20 T regulatory cells (TREG)(TCD4+CD25+FOXP3+) distribution in the different clinical forms of leprosy and reactional states() Parente, José Napoleão Tavares Talhari, Carolina Schettini, Antônio Pedro Mendes Massone, Cesare An Bras Dermatol Investigation BACKGROUND: Leprosy is characterized histologically by a spectrum of different granulomatous skin lesions, reflecting patients' immune responses to Mycobacterium leprae. Although CD4+CD25+ FoxP3+ T regulatory cells are pivotal in the immuneregulation, presence, frequency, and distribution of Tregs in leprosy, its reactional states have been investigated in few studies. OBJECTIVES: This study aimed to verify the frequency and distribution of regulatory T cells in different clinical forms and reactional states of leprosy. METHODS: We performed an immunohistochemical study on 96 leprosy cases [Indeterminate (I): 9 patients; tuberculoid tuberculoid: 13 patients; borderline tuberculoid: 26 patients; borderline borderline: 3 patients; borderline lepromatous: 8 patients; lepromatous lepromatous: 27 patients; reversal reaction: 8 patients; and erythema nodosum leprosum: 2 patients]. RESULTS: FoxP3-positive cells were present in 100% of the cases with an average density of 2.82% of the infiltrate. Their distribution was not related to granulomatous structures or special locations. There was a statistically significant increment of FoxP3 expression in patients with leprosy reversal reactions when compared with patients presenting with type I leprosy (P= 0.0228); borderline tuberculoid leprosy (P = 0.0351) and lepromatous leprosy (P = 0.0344). CONCLUSIONS: These findings suggest that Tregs play a relevant role in the etiopathogenesis of leprosy, mainly in type I leprosy reaction. Sociedade Brasileira de Dermatologia 2015 /pmc/articles/PMC4323697/ /pubmed/25672298 http://dx.doi.org/10.1590/abd1806-4841.20153311 Text en ©2015 by Anais Brasileiros de Dermatologia 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 | Investigation Parente, José Napoleão Tavares Talhari, Carolina Schettini, Antônio Pedro Mendes Massone, Cesare T regulatory cells (TREG)(TCD4+CD25+FOXP3+) distribution in the different clinical forms of leprosy and reactional states() |
title | T regulatory cells (TREG)(TCD4+CD25+FOXP3+) distribution in the different
clinical forms of leprosy and reactional states() |
title_full | T regulatory cells (TREG)(TCD4+CD25+FOXP3+) distribution in the different
clinical forms of leprosy and reactional states() |
title_fullStr | T regulatory cells (TREG)(TCD4+CD25+FOXP3+) distribution in the different
clinical forms of leprosy and reactional states() |
title_full_unstemmed | T regulatory cells (TREG)(TCD4+CD25+FOXP3+) distribution in the different
clinical forms of leprosy and reactional states() |
title_short | T regulatory cells (TREG)(TCD4+CD25+FOXP3+) distribution in the different
clinical forms of leprosy and reactional states() |
title_sort | t regulatory cells (treg)(tcd4+cd25+foxp3+) distribution in the different
clinical forms of leprosy and reactional states() |
topic | Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323697/ https://www.ncbi.nlm.nih.gov/pubmed/25672298 http://dx.doi.org/10.1590/abd1806-4841.20153311 |
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