Newswise — Bethesda, Md. (September 6, 2016)—Researchers have isolated an enzyme from bacteria present in human saliva that has potential as a therapy for celiac disease (CD), an autoimmune disorder that causes severe digestive and other health problems among sufferers when they consume gluten. An estimated 3 million people in the U.S. have celiac disease. Currently, the main course of treatment for people with CD is adherence to a strict gluten-free diet. The study, published in the American Journal of Physiology—Gastrointestinal and Liver Physiology, was chosen as an APSselect article for September.
“Gluten are proline- and glutamine-rich proteins present in wheat, barley and rye, and contain the immunogenic sequences that drive celiac disease (CD),” the researchers wrote. In other words, the immune response in the small intestine goes into overdrive when people with CD eat gluten.
Many patients find sticking to a gluten-free diet difficult—in part because gluten is present in most refined foods—and damaging to their quality of life. The search for new CD treatments has focused on methods that target the peptides in gluten that cause the immune system to overreact. This includes vaccine-based strategies and the use of enzymes that break down gluten and its immune-aggravating components before gluten reaches the small intestine.
The research team, led by researchers at Boston University’s Henry M. Golden School of Dental Medicine, wrote, “The aim was to isolate and identify the enzymes and evaluate their potential as novel enzyme therapeutics for CD. We have found that exceptionally high gluten-degrading enzyme activities are naturally associated with bacteria that colonize the oral cavity.”
Rothia bacteria, found in human saliva, can break down gluten compounds that cause an exaggerated immune response and that are typically resistant to the digestive enzymes that mammals produce. The team isolated a new class of enzymes—gluten-degrading enzymes from Rothia mucilaginosa, an oral microbial colonizer—from Rothia bacteria.
The identified Rothia enzymes belong to the same class as food-grade Bacillus enzymes. “B. subtilis is food safe and has been consumed for decades, e.g. in a product called natto, a Japanese fermented soy bean dish,” the researchers wrote. “Despite a long history of consumption of B. subtilis and its products, there are very few reports of adverse events. The food-grade status of B. subtilis, and the already widely consumed natto products, open new avenues for potential therapeutic applications of the subtilisin enzymes.”
The researchers concluded, “Going forward, since gluten-degrading enzymes are the preferred therapy of choice for CD, and given the exceptional activity of the subtilisins and their association with natural human microbial colonizers, they are worthy of further exploration for clinical applications in CD and potentially other gluten-intolerance disorders.”
The article “Identification of food-grade subtilisins as gluten-degrading enzymes to treat celiac disease” is published in the American Journal of Physiology—Gastrointestinal and Liver Physiology. It is highlighted as one of this month’s “best of the best” as part of the American Physiological Society’s APSselect program. Read all of this month’s selected research articles on the APSselect website.
NOTE TO JOURNALISTS: To schedule an interview with a member of the research team, please contact the APS Communications Office or 301-634-7209. Find more research highlights in the APS Press Room.
Physiology is the study of how molecules, cells, tissues and organs function in health and disease. Established in 1887, the American Physiological Society (APS) was the first U.S. society in the biomedical sciences field. The Society represents more than 11,000 members and publishes 14 peer-reviewed journals with a worldwide readership.
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