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http://hdl.handle.net/1843/56335| Tipo: | Artigo de Periódico |
| Título: | Eosinophil-Associated Innate IL-17 response promotes Aspergillus fumigatus Lung Pathology |
| Autor(es): | 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 |
| Resumen: | 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. |
| Asunto: | Eosinofilos Infecção Imunidade |
| Idioma: | por |
| País: | Brasil |
| Editor: | Universidade Federal de Minas Gerais |
| Sigla da Institución: | UFMG |
| Departamento: | 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 |
| Tipo de acceso: | Acesso Aberto |
| Identificador DOI: | https://doi.org/10.3389/fcimb.2018.00453 |
| URI: | http://hdl.handle.net/1843/56335 |
| Fecha del documento: | 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 |
| Aparece en las colecciones: | Artigo de Periódico |
archivos asociados a este elemento:
| archivo | Descripción | Tamaño | Formato | |
|---|---|---|---|---|
| Eosinophil-Associated Innate IL-17 Response Promotes Aspergillus fumigatus Lung Pathology.pdf | 47.29 MB | Adobe PDF | Visualizar/Abrir |
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