4.7 Article

Eosinophils release extracellular DNA traps in response to Aspergillus fumigatus

期刊

出版社

MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2017.07.048

关键词

Eosinophil; extracellular DNA traps; allergic bronchopulmonary aspergillosis; inflammation

资金

  1. Fundacao de Amparo a Pesquisa do Estado do Rio de Janeiro (FAPERJ)
  2. Fundacao de Amparo a Pesquisa do Estado de Minas Gerais (FAPEMIG)
  3. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)
  4. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)
  5. Research Grant on Allergic Disease and Immunology from the Japan Agency for Medical Research and Development
  6. Charitable Trust Laboratory Medicine Research Foundation of Japan
  7. JSPS [15KK0329, 16K08926]

向作者/读者索取更多资源

Background: Eosinophils mediate the immune response in different infectious conditions. The release of extracellular DNA traps (ETs) by leukocytes has been described as an innate immune response mechanism that is relevant in many disorders including fungal diseases. Different stimuli induce the release of human eosinophil ETs (EETs). Aspergillus fumigatus is an opportunistic fungus that may cause eosinophilic allergic bronchopulmonary aspergillosis (ABPA). It has been reported that eosinophils are important to the clearance of A fumigatus in infected mice lungs. However, the immunological mechanisms that underlie the molecular interactions between A fumigatus and eosinophils are poorly understood. Objective: Here, we investigated the presence of EETs in the bronchial mucus plugs of patients with ABPA. We also determined whether A fumigatus induced the release of human eosinophil EETs in vitro. Methods: Mucus samples of patients with ABPA were analyzed by light and confocal fluorescence microscopy. The release of EETs by human blood eosinophils was evaluated using different pharmacological tools and neutralizing antibodies by fluorescence microscopy and a fluorimetric method. Results: We identified abundant nuclear histone-bearing EETs in the bronchial secretions obtained from patients with ABPA. In vitro, we demonstrated that A fumigatus induces the release of EETs through a mechanism independent of reactive oxygen species but associated with eosinophil death, histone citrullination, CD11b, and the Syk tyrosine kinase pathway. EETs lack the killing or fungistatic activities against A fumigatus. Conclusions: Our findings may contribute to the understanding of how eosinophils recognize and act as immune cells in response to A fumigatus, which may lead to novel insights regarding the treatment of patients with ABPA.

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