Abnormalities in the Pulmonary Innate Immune System in Cystic Fibrosis

Pulmonary infection is the dominant clinical feature of cystic fibrosis (CF), but the basis for this susceptibility remains incompletely understood. One hypothesis is that CF airway surface liquid (ASL) is abnormal and interferes with neutrophil function. To study this possibility, we developed an i...

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Main Authors: Moraes, Theo J., Plumb, Jonathan, Martin, Raiza, Vachon, Eric, Cherepanov, Vera, Koh, Adeline, Loeve, Carola, Jongstra-Bilen, Jenny, Zurawska, Joanna H., Kus, Julianne V., Burrows, Lori L., Grinstein, Sergio, Downey, Gregory P.
Formato: Artigo
Idioma:Inglês
Publicado: American Thoracic Society 2006
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Articles
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC2644201/
https://ncbi.nlm.nih.gov/pubmed/16293782
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1165/rcmb.2005-0146OC
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