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Ethanol impairs mucosal immunity against Streptococcus pneumoniae infection by disrupting interleukin 17 gene expression.
Trevejo-Nunez, Giraldina; Chen, Kong; Dufour, Jason P; Bagby, Gregory J; Horne, William T; Nelson, Steve; Kolls, Jay K.
Afiliación
  • Trevejo-Nunez G; Richard King Mellon Foundation Institute for Pediatric Research, Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Chen K; Richard King Mellon Foundation Institute for Pediatric Research, Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Dufour JP; Division of Comparative Pathology, Tulane National Primate Research Center, Covington, Louisiana, USA.
  • Bagby GJ; Department of Medicine and Department of Physiology, LSU Health Sciences Center, New Orleans, Louisiana, USA.
  • Horne WT; Richard King Mellon Foundation Institute for Pediatric Research, Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Nelson S; Department of Medicine and Department of Physiology, LSU Health Sciences Center, New Orleans, Louisiana, USA.
  • Kolls JK; Richard King Mellon Foundation Institute for Pediatric Research, Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA jay.kolls@chp.edu.
Infect Immun ; 83(5): 2082-8, 2015 May.
Article en En | MEDLINE | ID: mdl-25754201
Acute ethanol intoxication suppresses the host immune responses against Streptococcus pneumoniae. As interleukin 17 (IL-17) is a critical cytokine in host defense against extracellular pathogens, including S. pneumoniae, we hypothesized that ethanol impairs mucosal immunity against this pathogen by disrupting IL-17 production or IL-17 receptor (IL-17R) signaling. A chronic ethanol feeding model in simian immunodeficiency virus (SIV)-infected rhesus macaques and acute ethanol intoxication in a murine model were used. Transcriptome analysis of bronchial brushes in the nonhuman primate model showed downregulation of the expression of IL-17-regulated chemokines in ethanol-fed animals, a finding also replicated in the murine model. Surprisingly, recombinant CXCL1 and CXCL5 but not IL-17 or IL-23 plus IL-1ß rescued bacterial burden in the ethanol group to control levels. Taken together, the results of this study suggest that ethanol impairs IL-17-mediated chemokine production in the lung. Thus, exogenous luminal restoration of IL-17-related chemokines, CXCL1 and CXCL5, improves host defenses against S. pneumoniae.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones Neumocócicas / Streptococcus pneumoniae / Expresión Génica / Inmunidad Mucosa / Interleucina-17 / Etanol / Membrana Mucosa Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Animals Idioma: En Revista: Infect Immun Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones Neumocócicas / Streptococcus pneumoniae / Expresión Génica / Inmunidad Mucosa / Interleucina-17 / Etanol / Membrana Mucosa Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Animals Idioma: En Revista: Infect Immun Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos