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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Detalhes bibliográficos
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 em: American Thoracic Society 2006
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Articles
Acesso em linha: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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