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.
Format: Artigo
Sprog:Inglês
Udgivet: American Thoracic Society 2006
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Articles
Online adgang: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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