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Whole blood profiling of leprosy type 1(reversal) reactions highlights prominence of innate immune response genes

BACKGROUND: The major factors contributing for nerve damage and permanent disabilities in leprosy are type 1 or reversal reactions (RR) and type 2 or erythema nodosum leprosum (ENL). Gene profiling of leprosy reactions have shown that different pathways are activated during the course of reactions,...

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Autores principales: Rêgo, Jamile Leão, de Lima Santana, Nadja, Machado, Paulo Roberto Lima, Ribeiro-Alves, Marcelo, de Toledo-Pinto, Thiago Gomes, Castellucci, Léa Cristina, Moraes, Milton Ozório
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109344/
https://www.ncbi.nlm.nih.gov/pubmed/30143000
http://dx.doi.org/10.1186/s12879-018-3348-6
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author Rêgo, Jamile Leão
de Lima Santana, Nadja
Machado, Paulo Roberto Lima
Ribeiro-Alves, Marcelo
de Toledo-Pinto, Thiago Gomes
Castellucci, Léa Cristina
Moraes, Milton Ozório
author_facet Rêgo, Jamile Leão
de Lima Santana, Nadja
Machado, Paulo Roberto Lima
Ribeiro-Alves, Marcelo
de Toledo-Pinto, Thiago Gomes
Castellucci, Léa Cristina
Moraes, Milton Ozório
author_sort Rêgo, Jamile Leão
collection PubMed
description BACKGROUND: The major factors contributing for nerve damage and permanent disabilities in leprosy are type 1 or reversal reactions (RR) and type 2 or erythema nodosum leprosum (ENL). Gene profiling of leprosy reactions have shown that different pathways are activated during the course of reactions, which is consistent with the exacerbated immune response exhibited by these patients. METHODS: We used qPCR to screen a panel of 90 genes related to the immune response in leprosy in RNA-derived peripheral leukocytes of patients with (N = 94) and without leprosy reactions (N = 57) in order to define expression signatures correlated to RR or ENL. RESULTS: Our results show that there is a marked signature for RR in the blood, comprising genes mostly related to the innate immune responses, including type I IFN components, autophagy, parkins and Toll like receptors. On the other hand, only Parkin was differentially expressed in the ENL group. CONCLUSIONS: The data put together corroborates previous work that brings evidence that an acute uncontrolled exacerbated immune response designed to contain the spread of M. leprae antigens might be cause of RR pathogenesis. Identifying a blood profile useful to predict leprosy reactions prior to its development might help to reduce the morbidity associated to this disabling disease.
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spelling pubmed-61093442018-08-29 Whole blood profiling of leprosy type 1(reversal) reactions highlights prominence of innate immune response genes Rêgo, Jamile Leão de Lima Santana, Nadja Machado, Paulo Roberto Lima Ribeiro-Alves, Marcelo de Toledo-Pinto, Thiago Gomes Castellucci, Léa Cristina Moraes, Milton Ozório BMC Infect Dis Research Article BACKGROUND: The major factors contributing for nerve damage and permanent disabilities in leprosy are type 1 or reversal reactions (RR) and type 2 or erythema nodosum leprosum (ENL). Gene profiling of leprosy reactions have shown that different pathways are activated during the course of reactions, which is consistent with the exacerbated immune response exhibited by these patients. METHODS: We used qPCR to screen a panel of 90 genes related to the immune response in leprosy in RNA-derived peripheral leukocytes of patients with (N = 94) and without leprosy reactions (N = 57) in order to define expression signatures correlated to RR or ENL. RESULTS: Our results show that there is a marked signature for RR in the blood, comprising genes mostly related to the innate immune responses, including type I IFN components, autophagy, parkins and Toll like receptors. On the other hand, only Parkin was differentially expressed in the ENL group. CONCLUSIONS: The data put together corroborates previous work that brings evidence that an acute uncontrolled exacerbated immune response designed to contain the spread of M. leprae antigens might be cause of RR pathogenesis. Identifying a blood profile useful to predict leprosy reactions prior to its development might help to reduce the morbidity associated to this disabling disease. BioMed Central 2018-08-24 /pmc/articles/PMC6109344/ /pubmed/30143000 http://dx.doi.org/10.1186/s12879-018-3348-6 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 Article
Rêgo, Jamile Leão
de Lima Santana, Nadja
Machado, Paulo Roberto Lima
Ribeiro-Alves, Marcelo
de Toledo-Pinto, Thiago Gomes
Castellucci, Léa Cristina
Moraes, Milton Ozório
Whole blood profiling of leprosy type 1(reversal) reactions highlights prominence of innate immune response genes
title Whole blood profiling of leprosy type 1(reversal) reactions highlights prominence of innate immune response genes
title_full Whole blood profiling of leprosy type 1(reversal) reactions highlights prominence of innate immune response genes
title_fullStr Whole blood profiling of leprosy type 1(reversal) reactions highlights prominence of innate immune response genes
title_full_unstemmed Whole blood profiling of leprosy type 1(reversal) reactions highlights prominence of innate immune response genes
title_short Whole blood profiling of leprosy type 1(reversal) reactions highlights prominence of innate immune response genes
title_sort whole blood profiling of leprosy type 1(reversal) reactions highlights prominence of innate immune response genes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109344/
https://www.ncbi.nlm.nih.gov/pubmed/30143000
http://dx.doi.org/10.1186/s12879-018-3348-6
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