Researchers at the University of Colorado Anschutz Medical Campus report that they have broken up deadly mucus secretions in the lungs, which can be fatal for asthma patients, at the molecular level and reversed their impacts.

In a study “Disulfide disruption reverses mucus dysfunction in allergic airway disease” published in Nature Communications, the scientists explained how they created an inhaled treatment that disrupted the production of excess mucus by reducing disulfide bonds in mice and opening up their airways. The same treatment had similar impacts on human mucus samples.

“Current asthma treatments have minimal effects on mucus, and the lack of therapeutic options stems from a poor understanding of mucus function and dysfunction at a molecular level and in vivo. Biophysical properties of mucus are controlled by mucin glycoproteins that polymerize covalently via disulfide bonds. Once secreted, mucin glycopolymers can aggregate, form plugs, and block airflow,” write the investigators.

“Here we show that reducing mucin disulfide bonds disrupts mucus in human asthmatics and reverses pathological effects of mucus hypersecretion in a mouse allergic asthma model. In mice, inhaled mucolytic treatment loosens mucus mesh, enhances mucociliary clearance, and abolishes airway hyperreactivity (AHR) to the bronchoprovocative agent methacholine. AHR reversal is directly related to reduced mucus plugging. These findings establish grounds for developing treatments to inhibit effects of mucus hypersecretion in asthma.”

“Currently about 10% of the population has asthma,” said the study’s lead author Christopher Evans, PhD, professor of Pulmonary Sciences & Critical Care at the CU School of Medicine. “Excessive mucus blocks airflow, causing wheezing, and worsening the effects of inflammation and contraction of the muscles that line the airways.”

Yet treatments for asthma like bronchodilators and steroids are rarely effective against mucus. Evans said they hydrate the mucus making it easier to cough up, but fail to treat the problem at the molecular level.

He and his team targeted polymeric mucin glycoproteins which help protect the lungs and airways from infection in healthy individuals. But when overproduced, they can make gelatinous plugs that block airways as seen in asthma and other pulmonary conditions.

The researchers tried to shut down this process by breaking up mucin disulfide bonds which contribute to the overproduction of mucus. They treated asthmatic mice with a chemical known as TCEP (tris(2-carboxyethyl)phosphine) which quickly reversed the disease. It also worked on human mucus taken as samples from asthma patients.

“We showed that disrupting mucin disulfide bonds loosens the mucus and reverses the pathological effects of mucus hypersecretion in a mouse allergic asthma model,” said study co-author Ana Maria Jaramillo, PhD, a postdoctoral fellow at CU Anschutz. “Loosening the mucus reduces airway inflammation, enhances mucociliary clearance and abolishes airway hyperactivity.”

The researchers said that while TCEP would likely irritate human lungs, something similar could be added to drugs treating asthma, COPD, cystic fibrosis, and other pulmonary diseases making them much more effective at reducing mucus.

“You can develop safer mucolytic compounds using this kind of strategy,” Evans said. “They could help steroids and albuterol penetrate deeper into the lungs and airways. They could be used as an adjunct therapy.”

Such new compounds might also be used in treating COPD, pulmonary fibrosis and even infections such as pneumonia or COVID-19 which attacks the lungs and airways.

“These findings establish grounds for developing treatments to inhibit effects of mucus hypersecretion in asthma,” Evans said. “I believe they have life-saving potential.”

Previous articleMechanisms Underlying SARS-CoV-2 Neuroinvasion Discovered
Next articleBioinformatic Study Underscores Contribution of Tandem Repeat Mutations in Autism