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Congrats Mohamed on your first authored JEM paper

Scientists discover natural molecules that help calm immune cells

First author on the JEM publication, Monash BDI PhD student Mohamed Abdelaal, and co-senior and co-corresponding author, Dr. Wael Awad.

Researchers have uncovered a surprising way the human body helps keep its immune system in check. The study found that when the body breaks down vitamin B2 (riboflavin), it produces natural molecules that can reduce the activity of MAIT cells – specialised immune cells involved in inflammation.

Co-led by Monash Biomedicine Discovery Institute (BDI) and University of Melbourne researchers, and published in the Journal of Experimental Medicine, the discovery shows that our bodies naturally produce molecules that can suppress MAIT cell activity, filling a major gap in understanding how the body maintains immune balance. Previously, research focused on how bacteria activate these cells, but little was known about the body’s own regulatory mechanisms.

These molecules interact with an immune sensor called MR1, which normally helps activate MAIT cells. Instead of boosting MR1 activity like vitamin-related molecules do, the body’s own molecules keep MR1 inside the cell, lowering its presence on the surface and dampening the immune response.

“Our findings reveal a natural mechanism that prevents unnecessary immune activation and inflammation,” said Mohamed Abdelaal, a PhD student with the Monash BDI and first author of the study.

“Understanding this process opens the door to new ways of controlling inflammation and immune-related diseases, by targeting overactive immune responses,” he said.

The study highlights a new dimension of MR1 biology and its role in immune homeostasis, paving the way for future research into how metabolic byproducts influence immunity.

Next steps include testing these molecules in living systems and exploring drug-like compounds that fine-tune MAIT cell activity, potentially leading to new therapeutic targets for immune disorders.

This study was co-led by Dr Wael Awad from Monash University’s Biomedicine Discovery Institute, and Dr Nicholas Gheradin from the Peter Doherty Institute for Infection and Immunity, University of Melbourne.

Read the full paper published in the Journal of Experimental Medicine, titled The antigen presenting molecule MR1 binds host-generated riboflavin catabolites.
DOI: 10.1084/jem.20250711

Original article

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Where there is smoke …. there is fire – Congrats to co-first author Wael

Researchers discover how cigarette smoke impairs critical lung immune cells

Cigarette smoking is widespread and deadly, yet our understanding of how cigarette smoke actually causes serious respiratory illnesses in incomplete, which has severely hampered the development of effective treatments. In the Journal of Experimental Medicine (JEM) Australian researchers reveal how multiple chemicals found in cigarette smoke and e-cigarettes alter the function of a key type of immune cell found in the lungs.

The study suggests that these alterations make cigarette smokers, and those exposed to second- and third-hand smoke, more susceptible to respiratory infections, and exacerbate smoking-related inflammatory diseases such as chronic obstructive pulmonary disease (COPD).

Cigarette smoking is known to impair the immune system’s response to infections and promote inflammation in the lungs that can lead to or exacerbate COPD, the third leading cause of death worldwide. COPD patients are more susceptible to influenza infections that can, in turn, exacerbate 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, 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,” says Dr Awad, first author on the new JEM study.

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 recognizes chemicals produced by bacteria and presents them at the surface of infected cells in order to activate MAIT cells and initiate an immune response. “We suspected that some of the more than 20,000 chemicals present in cigarette smoke that smokers inhale might also bind to MR1 and influence the activity of MAIT cells in the lungs”, Dr Awad said.

The researchers used computer modeling to predict which components of cigarette smoke might be recognized by MR1 and then found that several of these molecules not only bound to the protein but also either increased or decreased in amounts on the surface of cells. These chemicals, including benzaldehyde derivatives that are also used as flavorings in e-cigarettes, blocked activation of human MAIT cells by compounds produced by bacteria.

Unveiling the Molecular Impact of Smoking on Lung Health. This illustration explores how smoke components in cigarette and e-cigarette smoke obscures critical chemicals that bind MR1 and disrupt T cell functions in the lungs. Image: Erica Tandori

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.

“We found that mice lacking MAIT cells were also protected from cigarette smoke-induced COPD, showing reduced levels of lung inflammation and no tissue deterioration in their lung’s air sacs” Profesor Hansbro said.  “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” Awad says. 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.

Read the full paper in Journal of Experimental Medicine: Cigarette smoke components modulate the MR1-MAIT axis. DOI: 10.1084/jem.20240896

Original article

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