Cargando…
Intrinsic predisposition of naïve cystic fibrosis T cells to differentiate towards a Th17 phenotype
BACKGROUND: Cystic fibrosis (CF) is a complex, multi-system, life-shortening, autosomal recessive disease most common among Caucasians. Pulmonary pathology, the major cause of morbidity and mortality in CF, is characterized by dysregulation of cytokines and a vicious cycle of infection and inflammat...
Autores principales: | Kushwah, Rahul, Gagnon, Stéphane, Sweezey, Neil B |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3890528/ https://www.ncbi.nlm.nih.gov/pubmed/24344776 http://dx.doi.org/10.1186/1465-9921-14-138 |
Ejemplares similares
-
T cell unresponsiveness in a pediatric cystic fibrosis patient: a case report
por: Kushwah, Rahul, et al.
Publicado: (2014) -
Estrogen aggravates inflammation in Pseudomonas aeruginosa pneumonia in cystic fibrosis mice
por: Wang, Yufa, et al.
Publicado: (2010) -
Progression of Cystic Fibrosis Lung Disease from Childhood to Adulthood: Neutrophils, Neutrophil Extracellular Trap (NET) Formation, and NET Degradation
por: Khan, Meraj A., et al.
Publicado: (2019) -
Adult Non-Cystic Fibrosis Bronchiectasis Is Characterised by Airway Luminal Th17 Pathway Activation
por: Chen, Alice C.-H., et al.
Publicado: (2015) -
High Peripheral Blood Th17 Percent Associated with Poor Lung Function in Cystic Fibrosis
por: Mulcahy, Emily M., et al.
Publicado: (2015)