Researchers identify novel immune cells that may worsen asthma

Hamilton, ON (January 15, 2025) – Researchers at McMaster University have made an important discovery in the field of asthma research, identifying a new population of immune cells that may play a crucial role in the severity of asthma symptoms.  

The study, published in Science Translational Medicine on Jan. 15, 2025, sheds light on the complex mechanisms behind severe asthma and opens new avenues for potential treatments. 

Asthma is a chronic respiratory condition characterized by inflammation and narrowing of the airways, leading to difficulty breathing. Severe asthma, which affects up to 10 per cent of the general asthma population, is particularly challenging to treat due to its resistance to standard therapies.  

“When you can’t breathe, nothing else matters,” says Roma Sehmi, senior and corresponding author of the paper and professor in the Department of Medicine at McMaster University. “Our Hamilton-based group has been world leaders in evaluating the type of inflammation in the airways using methods developed to sample and examine sputum. We sought to better understand the mechanisms behind severe asthma so that we can better treat these patients.” 

The research team recruited patients from St. Joseph’s Healthcare Hamilton and carried out experimental work in laboratories within McMaster University and the Firestone Institute for Respiratory Health (FIRH), a joint McMaster University-St. Joseph’s research institute. 

Researchers explored a unique group of immune cells in the airways of people with severe asthma. The cells, called c-kit+IL-17A+ ILC2s, can be likened to chameleons; they can change their characteristics and have traits of two different types of immune cells. The study found that these "intermediate ILC2s" are linked to the presence of two types of cells that cause inflammation and make asthma worse (eosinophils and neutrophils). 

The researchers discovered that people with severe asthma have these chameleon-like ILC2s that show markers of another cell type, ILC3, which are associated with a high number of neutrophils in the airways – often seen in difficult-to-treat severe asthma. The study also found growth factors that encourage the formation of these intermediate ILC2s, suggesting that controlling their levels could prevent too many neutrophils from accumulating and worsening asthma symptoms. 

The ability of ILC2s to change and take on features of ILC3s in the airways of asthma patients is a new discovery. This finding gives new insights into what drives severe asthma and points to potential new treatment targets. By understanding the role of these intermediate ILC2s, researchers hope to develop better treatments for patients with severe asthma who don't respond well to current therapies. 

“When asthma is associated with both eosinophils and neutrophils cells, individuals are generally less responsive to treatment with glucocorticosteroids – which are the mainstay of treatment for severe asthma. The findings from this research pave the way for discovering new therapeutic targets for difficult-to-treat asthma,” said Parameswaran Nair, co-corresponding author of the paper and professor in the Department of Medicine at McMaster University. 

The study is the result of over a decade of collaborative research between Sehmi’s and Nair’s labs. The study involved contributions from several key researchers, including first author Xiaotian (Tim) Ju, who recently completed his PhD in Sehmi’s lab and is now a postdoctoral fellow at the National Institutes of Health in Bethesda, Maryland. 

The study was funded in part by an educational grant from Hoffmann-La Roche and graduate scholarship awards from the MITACS accelerate program, Ontario Graduate Scholarship, and The Research Institute of St. Joe’s Hamilton. 

For interviews please contact the authors directly: 

Roma Sehmi, professor in the Department of Medicine at McMaster University 
sehmir@mcmaster.ca  

Parameswaran Nair, professor in the Department of Medicine at McMaster University 
parames@mcmaster.ca  

Photos of the authors can be found here.  

More information, including a copy of the paper, can be found online at the Science Translational Medicine press package at eurekalert.org/press/medpak/.  

For other inquiries: fhsmedia@mcmaster.ca