Busca avançada
Ano de início
Entree
(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Sleep deprivation predisposes allergic mice to neutrophilic lung inflammation

Texto completo
Autor(es):
Nunes, Jethe O. F. [1] ; Apostolico, Juliana de Souza [1] ; Andrade, David A. G. [1] ; Ruiz, Francieli S. [2] ; Fernandes, Edgar R. [1] ; Andersen, Monica L. [2] ; Keller, Alexandre C. [1, 3] ; Rosa, Daniela S. [1]
Número total de Autores: 8
Afiliação do(s) autor(es):
[1] Fed Univ Sao Paulo UNIFESP EPM, Dept Microbiol Immunol & Parasitol, Rua Botucatu 862, 4 Andar, Sao Paulo - Brazil
[2] Fed Univ Sao Paulo UNIFESP EPM, Dept Psychobiol, Sao Paulo - Brazil
[3] Fed Univ Sao Paulo UNIFESP EPM, Dept Med, Div Nephrol, Sao Paulo - Brazil
Número total de Afiliações: 3
Tipo de documento: Artigo Científico
Fonte: Journal of Allergy and Clinical Immunology; v. 141, n. 3, p. 1018+, MAR 2018.
Citações Web of Science: 4
Resumo

Background: Although different studies associated sleep deprivation (SD) with systemic inflammatory changes, the effect of sleep duration on the pathology of allergic chronic diseases is poorly understood. Objective: We sought to evaluate the influence of SD on allergen-induced pulmonary inflammation. Methods: Ovalbumin (OVA)-sensitized C57BL/6 mice were exposed to a first set of intranasal OVA challenge under SD or healthy sleep (HS) conditions, followed by a second OVA challenge, 1 week apart. Some groups were subjected to corticosteroid treatment with dexamethasone. Results: OVA-sensitized mice with SD had more severe airway inflammation than the allergic group with HS. Analysis of lung parenchyma revealed that the inflammation in allergic mice with SD was marked by an influx of neutrophils (mainly) and eosinophils and secretion of IL-6, TNF-alpha, and IL-17 in contrast to the eosinophilic inflammation and IL-4 production observed in allergic mice with HS. The same cytokine profile was observed in ex vivo culture of cervical lymph node cells and splenocytes, indicating that in allergic mice SD favors immune responses toward a proinflammatory TH17 profile. This idea is supported by the fact that disruption of IL-17 signaling (IL-17 receptor A(-/-)) prevented airway neutrophilia in allergic mice with SD. Furthermore, allergic mice with SD became refractory to corticosteroid treatment in contrast to the allergic group with HS. Conclusion: Collectively, our data show that sleep quality participates in the progression of allergen-induced eosinophilic lung inflammation to corticosteroid-refractory neutrophilic manifestation. (AU)

Processo FAPESP: 12/04692-1 - Estudo sobre o papel de respostas Th2 como fator de risco associado ao desenvolvimento da glomeruloesclerose segmentar e focal
Beneficiário:Alexandre de Castro Keller
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 14/15061-8 - Direcionamento in vivo de epitopos de linfócitos TCD4+ do HIV-1 para células dendríticas
Beneficiário:Daniela Santoro Rosa
Modalidade de apoio: Auxílio à Pesquisa - Regular