Gut Bacteria Links Crohn’s Disease To Spondyloarthritis
New research helps explain the connection between Crohn’s disease and joint pain. The findings could help physicians identify Crohn’s disease patients who are more likely to develop spondyloarthritis, enabling them to prescribe more effective therapies for both conditions.
Crohn’s disease, a type of inflammatory bowel disease (IBD) that causes abdominal pain and diarrhea, affects about 800,000 Americans.
New technology helped the researchers identify a type of E. coli bacteria found in people with Crohn’s disease that can trigger inflammation associated with spondyloarthritis. The researchers used fecal samples from patients with IBD to identify bacteria in the gut that were coated with antibodies called immunoglobulin-A (IgA) that fight infection.
Using flow cytometry, in which fluorescent probes are used to detect IgA-coated bacterial species, the researchers discovered that IgA-coated E. coli were abundant in fecal samples from patients with both Crohn’s disease and spondyloarthritis. Using both patient samples and mouse models, they then linked these bacteria to cells that help regulate inflammation, known as Th17 cells, in people with autoimmune disorders.
The study was led by principal investigator Dr. Randy Longman and scientists from the Jill Roberts Center for Inflammatory Bowel Disease at New York Presbyterian and Weill Cornell Medicine, microbiologists at Cornell University and rheumatologists at Hospital for Special Surgery.
The investigators found that patients with Crohn’s disease and spondyloarthritis had higher levels of Th17 cells, and that a protein called IL-23 triggers their activity.
With the recent FDA approval of an anti-IL-23 medication for Crohn’s disease called ustekinumab, the findings may help physicians select therapies that target symptoms of both the bowels and joints in these patients, Dr. Longman said.
“Just sequencing the gut flora gives you an inventory of the bacteria, but does not tell you how they are perceived by the host immune system. This approach is giving you a functional readout versus just an inventory,”
said co-author Dr. Kenneth Simpson, professor of small animal medicine at Cornell’s College of Veterinary Medicine whose laboratory characterized the E. coli identified in the study.
Crohn’s Disease Remission
Dr. Simpson noted that each collaborator provided unique expertise to uncover the findings:
“We knew there was smoke but we didn’t know where the fire was. If we can block the ability of bacteria to induce inflammation, we may be able to kick Crohn’s disease and spondyloarthritis into remission.”
Dr. Longman led the translational study along with co-author Dr. Ellen Scherl, director of the Roberts Center at New York-Presbyterian and Weill Cornell Medicine and the Jill Roberts Professor of Medicine at Weill Cornell Medicine, in collaboration with HSS rheumatologists and co-authors Dr. Lisa Mandl and Dr. Sergio Schwartzman.
“In IBD therapy, this is a step toward precision medicine—to be able to clinically and biologically characterize a subtype of disease and then select the medicine that would best fit the patient with this type of inflammation,” Dr. Longman added. “The results of this innovative study will start to inform our decision of which of our available medications will give the best chance of helping the individual patient.”
Initial funding for the work was provided by a Cornell University and Weill Cornell Medicine pilot seed grant to foster collaborations between researchers in Ithaca and New York City, and has since been funded by the New York Crohn’s Foundation, the Charina Endowment Fund, the Center for Advanced Digestive Care, the Jill Roberts Institute for Research in IBD, and the National Institutes of Health.
Image: Crohn’s disease bacteria drives arthritis. E. coli bacteria (red), which are abundant in the immunoglobulin-A-coated microbiota of patients with a Crohn’s disease-associated condition called spondyloarthritis, promote systemic inflammation. The blue circular structures depict the nuclei of cells called epithelial cells. Credit: Dr. Kenneth Simpson, Cornell University