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Immunomodulation in Cystic Fibrosis: Why and How?

Cystic fibrosis (CF) lung disease is characterized by unconventional mechanisms of inflammation, implicating a chronic immune response dominated by innate immune cells. Historically, therapeutic development has focused on the mutated cystic fibrosis transmembrane conductance regulator (CFTR), leadin...

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Dettagli Bibliografici
Pubblicato in:Int J Mol Sci
Autori principali: Giacalone, Vincent D., Dobosh, Brian S., Gaggar, Amit, Tirouvanziam, Rabindra, Margaroli, Camilla
Natura: Artigo
Lingua:Inglês
Pubblicazione: MDPI 2020
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7247557/
https://ncbi.nlm.nih.gov/pubmed/32397175
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21093331
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