Please use this identifier to cite or link to this item: http://hdl.handle.net/1843/56335
Type: Artigo de Periódico
Title: Eosinophil-Associated Innate IL-17 response promotes Aspergillus fumigatus Lung Pathology
Authors: Nathália Luísa Sousa de Oliveira Malacco
Frederico Marianetti Soriani
Milene Alvarenga Rachid
Isabella Luisa da Silva Gurgel
Tauany Rodrigues Moura
Pedro Henrique Ferreira Sucupira
Lirlândia Pires de Sousa
Daniele da Glória de Souza
Remo de Castro Russo
Mauro Martins Teixeira
Abstract: Aspergillus fumigatus is a common widespread microorganism with environmental, biological and clinical relevance. After inhalation, swollen conidia can germinate, colonize and invade pulmonary tissues. Eosinophils have been described as key cells in A. fumigatus lung infection. However, their specific role in protecting or damaging lung tissue as well as their relatioship among different A. fumigatus strains is poorly understood. Previously, it has been reported that eosinophils are able to produce IL17 and mediate an innate response that protected mice from infection using Af293 and CEA10 strains. Here, we have developed a set of new experiments with the CEA17-derived A1163 strain of A. fumigatus. Using 1dblGATA1 mice, we demonstrate that eosinophils produce IL-17 and are involved in control of neutrophil, macrophage and lymphocyte recruitment. We found that eosinophils also induce high levels of cytokines and chemokines, generating an intense inflammatory process. Eosinophils are responsible for increased pulmonary dysfunction and elevated lethality rates in mice. Curiously, fungal burden was not affected. To address the role of IL-17 signaling, pharmacological inhibition of this mediator in the airways with anti-IL-17 antibody was able to reduce inflammation in the airways and protect infected mice. In conclusion, our results demonstrate that eosinophils control IL-17-mediated response and contribute to lung pathology after A. fumigatus infection. Therefore, eosinophils may represent a potential target for controlling exacerbated inflammation and prevent tissue damage during this fungal infection.
Subject: Eosinofilos
Infecção
Imunidade
language: por
metadata.dc.publisher.country: Brasil
Publisher: Universidade Federal de Minas Gerais
Publisher Initials: UFMG
metadata.dc.publisher.department: FAR - DEPARTAMENTO DE ANÁLISES CLÍNICAS E TOXICOLÓGICAS
ICB - DEPARTAMENTO DE BIOQUÍMICA E IMUNOLOGIA
ICB - DEPARTAMENTO DE FARMACOLOGIA
ICB - DEPARTAMENTO DE FISIOLOGIA E BIOFÍSICA
ICB - DEPARTAMENTO DE PATOLOGIA
Rights: Acesso Aberto
metadata.dc.identifier.doi: https://doi.org/10.3389/fcimb.2018.00453
URI: http://hdl.handle.net/1843/56335
Issue Date: 2019
metadata.dc.url.externa: https://www.frontiersin.org/articles/10.3389/fcimb.2018.00453/full
metadata.dc.relation.ispartof: Frontiers in Cellular and Infection Microbiology
Appears in Collections:Artigo de Periódico

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