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Molecular Basis and Gene Therapies of Cystic Fibrosis
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Summary of Genes. Thirty years ago, the gene responsible for cystic fibrosis (CF), a recessive genetic disease caused by mutations in the cystic fibrosis transmembrane conductance regulator gene, was identified. This progress has considerably changed our understanding of the pathophysiology of CF and has paved the way for the development of novel and specific therapies for the disease. The CFTR gene contains 27 exons and is characterized by a frequent three base pair deletion of the p.Phe508del. As a result of collaborative work, today more than 2000 mutations have been reported in the gene, and their impact on protein function is now more evident and useful in designing new strategies to correct the gene defect. The field of gene therapy, as illustrated by Ziying Yan in this book, has worked on identifying an efficient vector system for the delivery of the wild-type CFTR gene to the lung. At the same time, animal models have been developed in mice, rats, rabbits, zebrafish, ferrets, and pigs to establish the efficacity of gene delivery. These animals are also of the utmost importance in testing new molecules as modulators or correctors to improve the CFTR lung function. During the last three decades, the epidemiology of CF has dramatically changed, as today cystic fibrosis is now a chronic adult pulmonary disease.
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Keywords
- airway basal cell
- baculovirus
- biomarker
- CFTR
- CFTR gene
- CFTR modulators
- CFTR variants
- CFTR-related disorders
- common and new pathogenic variants
- cyclophosphamide
- cystic fibrosis
- disease liability
- Drug development
- enterotoxin gene cluster
- ethnic Russian population
- Exosomes
- functional assay
- Gene Therapy
- genotype-guided therapy
- genotype-phenotype correlations
- gut–lung axis
- health policies
- Health Policy
- human nasal epithelial cells
- incidence
- insect cells
- Interprétation
- lentivirus
- Lung
- lung microbiome
- medicine
- Metagenomics
- microvesicles
- miRNA
- Molecular diagnosis
- MRSA
- newborn screening
- next generation sequencing
- next generation sequencing (NGS)
- organoids
- penetrance
- pre-clinical in vitro models
- primary cells
- proteostasis
- rAAV2/HBoV1
- small molecules
- Staphylococcus aureus
- superantigen
- Survival
- Transcriptomics
- transient immunosuppression
- trypsinogen
Links
DOI: 10.3390/books978-3-03943-684-2Editions