Monocytes from Cystic Fibrosis Patients Are Locked in an LPS Tolerance State: Down-Regulation of TREM-1 as Putative Underlying Mechanism

Cystic Fibrosis (CF) is an inherited pleiotropic disease that results from abnormalities in the gene that codes for the chloride channel, Cystic Fibrosis Transmembrane Conductance Regulator (CFTR). CF patients are frequently colonized by several pathogens, but the mechanisms that allow colonization...

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Detalles Bibliográficos
Autores principales: del Fresno, Carlos, Gómez-Piña, Vanesa, Lores, Vanesa, Soares-Schanoski, Alessandra, Fernández-Ruiz, Irene, Rojo, Blas, Alvarez-Sala, Rodolfo, Caballero-Garrido, Ernesto, García, Felipe, Veliz, Tania, Arnalich, Francisco, Fuentes-Prior, Pablo, García-Río, Francisco, López-Collazo, Eduardo
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442190/
https://www.ncbi.nlm.nih.gov/pubmed/18628981
http://dx.doi.org/10.1371/journal.pone.0002667

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