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Fibrosis: a distinguishing feature in the pathology of neural leprosy

BACKGROUND: Fibrosis in the peripheral nerve is the end stage of leprous neuropathy and the cause of the resulting permanent neural function impairments. Preventive measures to avoid this irreversible pathological state are a relief strategy for leprosy sufferers. OBJECTIVES: The present study descr...

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Autores principales: Antunes, Sérgio Luiz Gomes, Jardim, Márcia Rodrigues, Vital, Robson Teixeira, Pascarelli, Bernardo Miguel de Oliveira, Nery, José Augusto da Costa, Amadeu, Thaís Porto, Sales, Anna Maria, da Costa, Eduardo Alves Freire, Sarno, Euzenir Nunes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto Oswaldo Cruz, Ministério da Saúde 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6684007/
https://www.ncbi.nlm.nih.gov/pubmed/31389520
http://dx.doi.org/10.1590/0074-02760190056
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author Antunes, Sérgio Luiz Gomes
Jardim, Márcia Rodrigues
Vital, Robson Teixeira
Pascarelli, Bernardo Miguel de Oliveira
Nery, José Augusto da Costa
Amadeu, Thaís Porto
Sales, Anna Maria
da Costa, Eduardo Alves Freire
Sarno, Euzenir Nunes
author_facet Antunes, Sérgio Luiz Gomes
Jardim, Márcia Rodrigues
Vital, Robson Teixeira
Pascarelli, Bernardo Miguel de Oliveira
Nery, José Augusto da Costa
Amadeu, Thaís Porto
Sales, Anna Maria
da Costa, Eduardo Alves Freire
Sarno, Euzenir Nunes
author_sort Antunes, Sérgio Luiz Gomes
collection PubMed
description BACKGROUND: Fibrosis in the peripheral nerve is the end stage of leprous neuropathy and the cause of the resulting permanent neural function impairments. Preventive measures to avoid this irreversible pathological state are a relief strategy for leprosy sufferers. OBJECTIVES: The present study describes the frequency of fibrosis along with its characterisation and pathogenic development. METHODS: Six-hundred-and-thirteen nerve samples were sorted from 278 neural leprosy (NL) and 335 non-leprosy neuropathy patients (ON). The total number of samples was histologically examined by routine staining methods (haematoxylin-eosin, Wade staining and Gomori’s trichrome) and fibrosis was evaluated via semi-quantitative estimation. FINDINGS: Fibrosis was most frequent in the NL group (33% against 0.4% in ON) while fibrosis in association with endoneurial microfasciculation was found in 38 (41.3%) of the NL samples in the examination of semithin sections. Pericytic activation in the perivascular environment was confirmed to be the source of the fibroblasts and perineurial cells delimiting microfascicles. End-stage fibrosis in leprosy displays an arrangement of microfascicles devoid of neural components (i.e., Schwann cells and axons) lined by an intermediate phenotype of fibroblastic-perineurial cells filled with bundles of collagen fibres. MAIN CONCLUSIONS: The present study underscores that fibrosis is frequently the severe end stage of neural leprosy NL pathogeny after analysing the notably distinct development of fibrosis within the neural environment.
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spelling pubmed-66840072019-08-19 Fibrosis: a distinguishing feature in the pathology of neural leprosy Antunes, Sérgio Luiz Gomes Jardim, Márcia Rodrigues Vital, Robson Teixeira Pascarelli, Bernardo Miguel de Oliveira Nery, José Augusto da Costa Amadeu, Thaís Porto Sales, Anna Maria da Costa, Eduardo Alves Freire Sarno, Euzenir Nunes Mem Inst Oswaldo Cruz Original Article BACKGROUND: Fibrosis in the peripheral nerve is the end stage of leprous neuropathy and the cause of the resulting permanent neural function impairments. Preventive measures to avoid this irreversible pathological state are a relief strategy for leprosy sufferers. OBJECTIVES: The present study describes the frequency of fibrosis along with its characterisation and pathogenic development. METHODS: Six-hundred-and-thirteen nerve samples were sorted from 278 neural leprosy (NL) and 335 non-leprosy neuropathy patients (ON). The total number of samples was histologically examined by routine staining methods (haematoxylin-eosin, Wade staining and Gomori’s trichrome) and fibrosis was evaluated via semi-quantitative estimation. FINDINGS: Fibrosis was most frequent in the NL group (33% against 0.4% in ON) while fibrosis in association with endoneurial microfasciculation was found in 38 (41.3%) of the NL samples in the examination of semithin sections. Pericytic activation in the perivascular environment was confirmed to be the source of the fibroblasts and perineurial cells delimiting microfascicles. End-stage fibrosis in leprosy displays an arrangement of microfascicles devoid of neural components (i.e., Schwann cells and axons) lined by an intermediate phenotype of fibroblastic-perineurial cells filled with bundles of collagen fibres. MAIN CONCLUSIONS: The present study underscores that fibrosis is frequently the severe end stage of neural leprosy NL pathogeny after analysing the notably distinct development of fibrosis within the neural environment. Instituto Oswaldo Cruz, Ministério da Saúde 2019-08-05 /pmc/articles/PMC6684007/ /pubmed/31389520 http://dx.doi.org/10.1590/0074-02760190056 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License
spellingShingle Original Article
Antunes, Sérgio Luiz Gomes
Jardim, Márcia Rodrigues
Vital, Robson Teixeira
Pascarelli, Bernardo Miguel de Oliveira
Nery, José Augusto da Costa
Amadeu, Thaís Porto
Sales, Anna Maria
da Costa, Eduardo Alves Freire
Sarno, Euzenir Nunes
Fibrosis: a distinguishing feature in the pathology of neural leprosy
title Fibrosis: a distinguishing feature in the pathology of neural leprosy
title_full Fibrosis: a distinguishing feature in the pathology of neural leprosy
title_fullStr Fibrosis: a distinguishing feature in the pathology of neural leprosy
title_full_unstemmed Fibrosis: a distinguishing feature in the pathology of neural leprosy
title_short Fibrosis: a distinguishing feature in the pathology of neural leprosy
title_sort fibrosis: a distinguishing feature in the pathology of neural leprosy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6684007/
https://www.ncbi.nlm.nih.gov/pubmed/31389520
http://dx.doi.org/10.1590/0074-02760190056
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