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Scientists at the University of Virginia School of Medicine have identified immune cells vital for protecting us from potentially fatalClostridum difficileinfection. Surprisingly, those cells are often vilified for their role in causing asthma and allergies. But when it comes toC. difficile, they could be the difference in life and death.
With the discovery (“Microbiota-Regulated IL-25 Increases Eosinophil Number to Provide Protection duringClostridium difficileInfection”), published in Cell Reports, the researchers have answered some of the greatest questions aboutC. diff, shed light on why antibiotics lead to severeC. diffinfection, and identified a potential way for doctors to prevent the life-threatening infection and possibly other infections as well.
William A. Petri, Jr., M.D., Ph.D., chief of the Division of Infectious Diseases and International Health at the UVA Health System, hailed the discovery by UVA’s Erica L. Buonomo, Ph.D., and colleagues as “the most remarkable breakthrough I have participated in as a scientist.”
According to Dr. Petri, “Antibiotics are really important, and very often you have to give antibiotics, but you do it knowing that you’re predisposing your patient to another infection[C. difficile] that is potentially lethal. About one out of seven people with this infection dies in North America. So it’s a terrible dilemma for physicians. This is not a common complication of antibiotics, but when it happens, it’s a very serious one. This work enables a potential long-term solution to that, which is probiotics to restore the natural state of the gut.”
There were almost half a millionC. diffinfections in the United States in 2011, and approximately 29,000 patients died within 30 days of infection, according to a study released last year by the U.S. CDC. The agency has classified the bacterium as an “urgent threat,” noting the rise of a new epidemic strain in recent years that has made the infection even deadlier.
Kris Chadee, Ph.D., a professor at the University of Calgary who was not involved in UVA’sC. diffwork, called the discovery “as unexpected as it is important,” noting that the finding “has immediate implications for therapy. Probiotics designed to restore the healthy gut microbiome should be an effective way to prevent this life-threatening infection.”
C. difficileis primarily a hospital-acquired infection, and it predominantly affects the elderly, particularly elderly people on antibiotics. UVA’s discovery offers answers about why that is. The researchers showed that the gut bacteria stimulates the production of interleukin-25 (IL-25), which then recruits protective cells–eosinophils. As such, IL-25, the product of “good” bacteria, protects the lining of the gut from pathogens. Antibiotics, however, disrupt our body’s natural bacterial populations, leaving the gut lining vulnerable toC. diffand other infections.
Intriguingly, the researchers found an important and unexpected role for eosinophils, a type of white blood cell. These cells play a role in causing both allergies and asthma, but in the battle againstC. diff, they can be life-saving. IL-25, the UVA researchers show, protects us fromC. diffby manufacturing eosinophils to guard the integrity of the gut lining. The epidemic strain ofC. diffis so deadly specifically because it kills eosinophils, allowing it to breach the gut, the researchers determined.
“We found that if you deplete eosinophils, either genetically or by an antibody neutralization, you lost the integrity of the epithelial barrier in the gut,” Dr. Buonomo said. “Maintaining that barrier is very important for having a healthy response toC. difficile.It also prevents bacteria from spreading to other sites in the body, so if you have a breakdown in the barrier, you can have a septic response or bacteria in your blood or in other systemic organs.”
The findings suggest that researchers should be able to develop new probiotics that patients could take to ward offC. difficile. “We could end up that every person taking an antibiotic is taking a new probiotic that is specifically designed to maintain IL-25 and eosinophils,” noted Dr. Petri.