Scientists have discovered a new way to treat cystic fibrosis (CF) that involves delivering artificial proteins to patients lung cells to replace the faulty cystic fibrosis transmembrane conductance regulator (CFTR) protein.

The finding was reported in the study, Anion carriers as potential treatments for cystic fibrosis: transport in cystic fibrosis cells, and additivity to channel-targeting drugs, published recently in the journal Chemical Science.

CF is a genetic disorder caused by mutations in the CFTR gene, which provides instructions to make the CFTR protein.This protein works as a channel that transports in and out of cells molecules with a negative electrical charge (called anions), such as chloride, which have a direct impact on the regulation of water transport and the production of mucus.

In patients with CF, the transport of anions is impaired, leading to a buildup of fluid in the lungs and other organs.

One approach to restore anion transport to CF cells [utilizes] alternative pathways for transmembrane anion transport, including artificial anion carriers (anionophores), the researchers wrote.

The basic idea is to deliver these anionophores to patients lung cells, so that these artificial molecule transporters may replace the faulty CFTR protein, and restore the transport of water and salt in and out of cells, alleviating the symptoms of CF.

According to the researchers, these anionophores, unlike other types of targeted therapies that have been developed to correct specific defects in CFTR, may be used as a form of treatment for all CF patients, either alone or in combination with other CF therapies.

In their study, researchers from the University of Bristol in collaboration with investigators from the University of Southampton, both in the U.K., designed and tested 22 different anionophores.

Researchers discovered that four of these compounds (compound 11, 12, 15, and 19) were able to effectively transport anions in and out of lung cells cultured in a lab dish in a dose-dependent manner.

Moreover, they showed that all four compounds improved the transport of anions in cells that contained the F508 deletion, the most common CFTR mutation associated with CF, when used together with lumacaftor and ivacaftor, the active ingredients of two ofVertex Pharmaceuticals approved CF therapies, Orkambi and Kalydeco.

We also show that the compounds need not be toxic, which is an important issue, and that their activity can supplement the effects of recently introduced drugs, which help some CF patients through a different mechanism, Anthony Davis, from the University of Bristol and corresponding author of the study, said in a press release.

Overall, the results provide further evidence that anionophores, by themselves or together with other treatments that restore anion transport, offer a potential therapeutic strategy for CF, the researchers wrote.

Theres still a long way to go, but if the research proceeds as hoped it might lead to a genuinely effective and general treatment for CF patients over this timescale, Davis said.

Joana holds a MSc in Biology and a MSc in Evolutionary and Developmental Biology from Universidade de Lisboa. She is currently finishing her PhD in Biomedicine and Clinical Research at Universidade de Lisboa. Her work has been focused on the impact of non-canonical Wnt signaling in the collective behavior of endothelial cells cells that made up the lining of blood vessels found in the umbilical cord of newborns.

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Patrcia holds her PhD in Medical Microbiology and Infectious Diseases from the Leiden University Medical Center in Leiden, The Netherlands. She has studied Applied Biology at Universidade do Minho and was a postdoctoral research fellow at Instituto de Medicina Molecular in Lisbon, Portugal. Her work has been focused on molecular genetic traits of infectious agents such as viruses and parasites.

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Scientists Hope They Have Found New Form of Cystic Fibrosis Therapy - Cystic Fibrosis News Today

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