Systems serology in cystic fibrosis: Anti-Pseudomonas IgG1 responses and reduced lung function

Nearly one-half of patients with cystic fibrosis (CF) carry the homozygous F508del mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene but exhibit variable lung function phenotypes. How adaptive immunity influences their lung function remains unclear, particularly the ser...

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Detalles Bibliográficos
Autores principales: Lu, Shiping, Chen, Kong, Song, Kejing, Pilewski, Joseph M., Gunn, Bronwyn M., Poch, Katie R., Rysavy, Noel M., Vestal, Brian E., Saavedra, Milene T., Kolls, Jay K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10591031/
https://www.ncbi.nlm.nih.gov/pubmed/37852181
http://dx.doi.org/10.1016/j.xcrm.2023.101210

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10591031/
https://www.ncbi.nlm.nih.gov/pubmed/37852181
http://dx.doi.org/10.1016/j.xcrm.2023.101210

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