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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...
| Autores principales: | , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2023
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| Materias: | |
| 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 |