Reduced mucosal associated invariant T-cells are associated with increased disease severity and Pseudomonas aeruginosa infection in cystic fibrosis.
<h4>Background</h4>Primary defects in host immune responses have been hypothesised to contribute towards an inability of subjects with cystic fibrosis (CF) to effectively clear pulmonary infections. Innate T-lymphocytes provide rapid pathogen-specific responses prior to the development o...
Guardado en:
Autores principales: | Daniel J Smith, Geoffrey R Hill, Scott C Bell, David W Reid |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2014
|
Materias: | |
Acceso en línea: | https://doaj.org/article/2a087e3964c043a8ac54a64c5d843b3e |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
The susceptibility of Pseudomonas aeruginosa strains from cystic fibrosis patients to bacteriophages.
por: Christiane Essoh, et al.
Publicado: (2013) -
Evolution of the Pseudomonas aeruginosa mutational resistome in an international Cystic Fibrosis clone
por: Carla López-Causapé, et al.
Publicado: (2017) -
Lung and Gut Microbiota Changes Associated with <i>Pseudomonas aeruginosa</i> Infection in Mouse Models of Cystic Fibrosis
por: Giovanni Bacci, et al.
Publicado: (2021) -
Modifications of Pseudomonas aeruginosa cell envelope in the cystic fibrosis airway alters interactions with immune cells
por: Preston J. Hill, et al.
Publicado: (2017) -
The role of Psl in the failure to eradicate Pseudomonas aeruginosa biofilms in children with cystic fibrosis
por: Amanda J. Morris, et al.
Publicado: (2021)