Cystic Fibrosis: Pathogenesis and Future Treatment Strategies

被引:113
作者
Ratjen, Felix A. [1 ]
机构
[1] Univ Toronto, Hosp Sick Children, Div Resp Med Physiol & Expt Med, Toronto, ON M5G 1X8, Canada
关键词
cystic fibrosis; airway surface liquid; cystic fibrosis transmembrane regulator; CFTR; pharmacotherapy; chloride secretion; gene therapy; osmotic therapy; TRANSMEMBRANE CONDUCTANCE REGULATOR; INHALED HYPERTONIC SALINE; AIRWAY SURFACE LIQUID; MUCOCILIARY CLEARANCE; PERICILIARY LIQUID; CHLORIDE CHANNEL; EPITHELIAL-CELLS; CONTROLLED-TRIAL; GENE-TRANSFER; CFTR FUNCTION;
D O I
10.4187/aarc0427
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Since the detection of the underlying gene defect, our knowledge of how the genetic mutations in cystic fibrosis cause lung disease has increased substantially, but we still lack a complete understanding of some of the pieces in the puzzle. Nevertheless, the information gained has led to new therapeutic approaches that address key factors of cystic fibrosis pathophysiology. Past therapeutic successes were largely based on targeting the consequences of the cystic fibrosis transmembrane regulator dysfunction, such as phlegm retention, infection, and inflammation, but new therapies may be able to address the underlying abnormality rather than its downstream effects. The efficacy of these treatments still needs to be established, but early studies look promising for several compounds. This review summarizes our current understanding of the pathophysiology and treatment of cystic fibrosis lung disease.
引用
收藏
页码:595 / 602
页数:8
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