A NEW drug called Fevipiprant has a potential to lower asthmatic patients’ risks of suffering attack and being admitted to a hospital, according to a study.
Himanshu Kaul, postdoctoral fellow in University of British Columbia and one of the authors of the study published this report on an academic website The Conversation.
The new drug reduces airway smooth muscle mass— a key clinical indicator of disease severity that increases the likelihood of more frequent asthma attacks and even deaths.
The original trial was led by Christopher Brightling, clinical professor in respiratory medicine at the University of Leicester and the principal co-ordinator of the European Lung Foundation AirPROM.
According to Global Asthma Report 2018, asthma affects around 339 million people globally, killing not less than 1000 people daily.
The prevalence of asthma is on the rise, with low- and middle-income countries, including Nigeria, suffering most — in part, because essential medicines are unavailable, unaffordable or are of unreliable quality.
According to the Global Asthma Report, asthma is a big problem in Nigeria due to challenges faced from inadequate resources, weak health systems, and poverty.
Asthma is caused by complex set of interactions between a patient’s genes, cells and environment that lead to an increase in airway smooth muscle mass: a process referred to as “remodelling.”
The human airways are composed of several different cell types that exist together in a highly ordered state. The airway lumen is lined by epithelial cells and, further inside, the mesenchyme. The latter contains muscle cells that increase in mass during asthma.
Another crucial features of the airway are the inflammatory cells that are recruited in the event of a foreign challenge (such as an allergen or virus).
In health, these three elements work in harmony to ensure effective airflow and appropriate response to external challenges. In asthma, these harmonic interactions are compromised, resulting in increased muscle mass.
In the clinical trial for the new drug, Fevipiprant was observed to reduce the number of inflammatory cells and muscle mass.
To understand how, Himanshu Kaul said he developed a mathematical model that combined the epithelial, mesenchymal and inflammatory elements — to understand what is responsible for airway remodelling during asthma.
“I used something called ‘agent-based modeling’ — a mathematical approach that relies on rule-sets governing interactions between various model elements,” he wrote.
“I developed a “virtual patient” with severe asthma and gave them virtual drugs. I made sure that the model was capturing biological reality by first administering virtual Mepolizumab, which killed inflammatory cells in the airways. The virtual patient performance was consistent with clinical results.
“I then gave the virtual patient Fevipiprant. While it showed the same amount of reduction in inflammatory cells as the clinical trial, it failed to show the same amount of reduction in muscle mass as observed clinically.”
He said the process led to the conclusion that Fevipiprant acted not by reducing the inflammation alone, but by also directly impacting muscle mass.
Also Kaul said that experiments conducted by Ruth Saunders at the University of Leicester, with muscle cells taken from patients suggested that Fevipiprant reduced the recruitment of cells called myofibroblasts, which add to muscle mass during remodelling.
When this secondary feature was added to the model, the observed reduction in the muscle mass of the virtual patient was consistent with clinical data.
The postdoctoral fellow insisted that Fevipiprant could be a potential therapy to improve airway remodelling in asthma.
“Using this drug could allow patients to reduce their dependence on high-dose steroids, whose side-effects include weight gain, diabetes and high blood pressure,” Kaul said.
“Secondly, the “virtual patient” can play a role in drug design and optimization, potentially lowering drug-development costs.
“While this does need more testing with other therapies, it is a milestone in patient-specific models and promises a new era of precision within respiratory medicine.”