Over 20,000 chemicals in cigarette smoke may bind to immune cell MR1, affecting immune response.
Cigarette smoking is prevalent and harmful, but our understanding of how it leads to serious respiratory diseases remains limited, hindering the development of effective treatments. Today (TBC), Australian researchers uncover how various chemicals in cigarette smoke and e-cigarettes affect the function of a crucial immune cell in the lungs. (1✔ ✔Trusted Source
Cigarette smoke components modulate the MR-1-MAIT axis
Go to source) The study, published in the Journal of Experimental Medicine (JEM), suggests that these alterations make cigarette smokers, and those exposed to second- and third-hand smoke, more susceptible to respiratory infections, and worsen smoking-related inflammatory diseases such as chronic obstructive pulmonary disease (COPD).
‘#Smoking weakens your #lungs, making you more vulnerable to #infections and diseases like #COPD (chronic obstructive pulmonary disease). It's the third leading cause of death globally.’
Chronic Obstructive Pulmonary Disease
COPD patients are more susceptible to influenza infections that can, in turn, worsen the underlying disease by increasing airway inflammation and promoting the destruction of the lung’s air sacs. There are currently no effective treatments for COPD.According to Dr. Wael Awad, from Monash University’s Biomedicine Discovery Institute, first author on the new JEM study, “until now the mechanisms underlying the skewed immune responses in people exposed to cigarette smoke, and how they are related to smoke-associated diseases like COPD remain unclear.”
Professor Jamie Rossjohn of Monash University’s Biomedicine Discovery Institute co-led the study with Professor David P. Fairlie of the Institute for Molecular Bioscience at University of Queensland, Professor Alexandra J. Corbett of the University of Melbourne, based at the Peter Doherty Institute for Infection and Immunity, and Professor Philip M. Hansbro of the Centenary Institute and University of Technology Sydney.
In their study, the researchers looked at the effects of cigarette smoke on Mucosal-Associated Invariant T (MAIT) cells, a type of immune cell found in the lungs and other tissues of the body. MAIT cells help fight off bacterial and viral infections and can promote inflammation or tissue repair.
MAIT cells are activated by a protein called MR1 that is found in almost every cell of the body. MR1 recognises chemicals produced by bacteria and presents them at the surface of infected cells in order to activate MAIT cells and initiate an immune response. “While we know that smoke from cigarettes, bushfires, cooking, vehicle exhausts and burning waste pose significant health risks, we still surprisingly know relatively little about how the specific components pf smoke affect our immune system and how they impact multiple parts of the human body,” Professor Fairlie said.
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The research team then studied the effects of cigarette smoke on MAIT cells from human blood and mice and showed they reduced MAIT cell function. Mice repeatedly exposed to cigarette smoke developed symptoms of lung disease and this was worsened if also infected by influenza. Researchers found that long-term exposure to cigarette smoke altered the protection provided to mice by their MAIT cells, making them less able to fight off influenza infections and more prone to the development of COPD disease.
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“This study demonstrates the power of collaboration and the insights we can gain with inter-disciplinary science,” Professor Corbett said.
“Overall, our study reveals that components of cigarette smoke can bind to the protein MR1 and reduce the functions of protective immune cells called MAIT cells. This increases susceptibility to infections worsens progression of lung disease” Dr Awad said. The researchers now plan to investigate exactly which MAIT cell pathways are impacted by cigarette smoke, in order to learn how to better treat COPD and other lung diseases.
Reference:
- Cigarette smoke components modulate the MR-1-MAIT axis - (https://apps.crossref.org/pendingpub/pendingpub.html?doi=10.1084%2Fjem.20240896)