Targeting the immune system could prevent or treat periodontal disease (PD), a common but serious gum disease, according to new research from the University of Pittsburgh.
The study, published in Proceedings of the National Academy of Sciencesshowed that delivering microparticles containing the immunomodulatory compound CCL2 directly to the gingiva inhibited bone loss and accelerated bone repair in a mouse model of PD.
Dr. Charles Speir
“PD is a highly prevalent inflammatory disease that affects many patients in varying degrees of severity,” said senior author Dr. Charles Speir, associate professor and chair of the Department of Periodontology and Preventive Dentistry at Pitt. School of Dentistry and a member of McGowan Institute for Regenerative Medicine. “This research is exciting because it has the potential to impact so many people.”
Sfeir collaborated with Dr. Steven Little, Distinguished Professor and Chair of the Department of Chemistry and Petroleum Engineering at Swanson School of Engineering and member of McGowan, who developed microparticles that provide sustained release of CCL2.
Dr. Stephen Little
“The potential for mechanical systems to interact with the immune system of the periodontal space is huge and represents a completely different way of treating disease compared to what is done clinically now,” Little said. “This collaboration with Dr. Sfeir is further proof of the exciting future for these types of technologies.”
Led by first author Dr. Mostafa Shehabeldin, who was a graduate student in Sfeir’s lab and is now an assistant professor of periodontics at UT Health San Antonio, the researchers first induced PD in mice by tying a strand of silk around one of their molars. Silk quickly accumulates bacteria, causing inflammation that begins to rapidly destroy the bone around the teeth in as little as four days.
To see if CCL2 could prevent PD or treat active disease, the researchers treated animals with the microparticles at the same time as silk placement or four days after. They also tested whether CCL2 would affect the self-resolving disease by treating mice with microparticles at the same time as removing the silk.
In all three scenarios, CCL2 treatment helped prevent or treat PD by reducing bone loss and improving bone repair.
Microparticles containing the immunomodulatory compound CCL2 (CREDIT: Julie Kobyra)
This beneficial effect came from changes in macrophages, the white blood cells that kill microorganisms, remove dead cells, and stimulate other immune cells.
Injecting microparticles also altered the oral microbiome, reducing or preventing increases in total bacterial load and the abundance of certain bacterial species associated with PD.
“The treatment of PD has always focused on targeting the bacteria, but the bacteria don’t actually cause the disease. Instead, they cause PD by activating the immune system, which leads to inflammation and bone loss around the teeth,” Sfeir said. “Our study shows that it goes both ways: If we curb the immune system, we can change the composition of the bacteria and prevent the disease from occurring or stop it from progressing.”
According to Sfeir, who hopes to test this new approach to treating PD in a future clinical trial, CCL2 therapy will likely be developed as an adjunctive therapy that would work alongside traditional bacteria-targeting treatments that include regular dental cleanings and antimicrobials.
“For 70 to 80 percent of the PD population, they get a dental cleaning and the inflammation goes down,” Sfeir said. “But a small fraction of patients, despite regular cleanings and meticulous oral hygiene, still have bone destruction. For this aggressive PD, we still don’t have a good cure. This is where we think modulating the immune system with something like CCL2 would really help.”
The findings also offer new insights into understanding the interactions between the immune system and the microbiome.
“The oral cavity is one of the few areas of the human body where you can study interactions between microbes and the immune system, and it’s much more accessible than other areas like the gut and lungs,” Sfeir said. “This makes PD a really important model system for other immune-driven diseases.”
