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Review
. 2024 Sep 4;25(17):9599.
doi: 10.3390/ijms25179599.

Cystic Fibrosis: A Journey through Time and Hope

Affiliations
Review

Cystic Fibrosis: A Journey through Time and Hope

Pascal Trouvé et al. Int J Mol Sci. .

Abstract

Just over thirty years is the span of a generation. It is also the time that has passed since the discovery of the gene responsible for cystic fibrosis. Today, it is safe to say that this discovery has revolutionized our understanding, research perspectives, and management of this disease, which was, thirty years ago, a pediatric condition with a grim prognosis. The aim of this review is to present the advances that science and medicine have brought to our understanding of the pathophysiology of the disease and its management, which in many ways, epitomizes modern molecular genetic research. Since the discovery of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in 1989, modeling the CFTR protein, deciphering its function as an ion channel, and identifying its molecular partners have led to numerous therapeutic advances. The most significant advancement in this field has been the discovery of protein modulators that can target its membrane localization and chloride channel activity. However, further progress is needed to ensure that all patients can benefit from a therapy tailored to their mutations, with the primary challenge being the development of treatments for mutations leading to a complete absence of the protein. The present review delves into the history of the multifaceted world of CF, covering main historical facts, current landscape, clinical management, emerging therapies, patient perspectives, and the importance of ongoing research, bridging science and medicine in the fight against the disease.

Keywords: cystic fibrosis.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Chronology of the key findings demonstrating that understanding the pathophysiology of cystic fibrosis is a long process. A marked acceleration in the rate of significant discoveries has been observed since the 1930s.
Figure 2
Figure 2
Timeline of the main therapies implemented against cystic fibrosis correlated with the increase in life expectancy. Thanks to new treatments (CFTR modulators), cystic fibrosis is now a chronic adult disease.

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