{"id":941611,"date":"2026-05-06T13:32:16","date_gmt":"2026-05-06T13:32:16","guid":{"rendered":"https:\/\/www.europesays.com\/uk\/941611\/"},"modified":"2026-05-06T13:32:16","modified_gmt":"2026-05-06T13:32:16","slug":"scientists-flip-immune-system-switch-uncover-surprising-path-to-stop-gut-inflammation","status":"publish","type":"post","link":"https:\/\/www.europesays.com\/uk\/941611\/","title":{"rendered":"Scientists Flip Immune System \u201cSwitch,\u201d Uncover Surprising Path To Stop Gut Inflammation"},"content":{"rendered":"

\"Woman<\/a>Inflammatory bowel disease (IBD) is a chronic condition involving abnormal immune-driven inflammation of the gastrointestinal tract, most commonly seen in Crohn\u2019s disease and ulcerative colitis. It results from interactions between genetics, the immune system, and the gut microbiome. Credit: Shutterstock<\/p>\n

Scientists have uncovered an unexpected mechanism by which the gut\u2019s immune system maintains balance, challenging long-standing assumptions about how immune tolerance is regulated.<\/strong><\/p>\n

Researchers at Weill Cornell Medicine<\/a> have uncovered an unexpected mechanism the immune system uses to prevent chronic inflammation in the intestine. The discovery could point to new treatment strategies for inflammatory bowel disease (IBD), food allergies, and other autoimmune disorders.<\/p>\n

The study, published April 24 in the Journal of Experimental Medicine, examined how immune cells communicate to tolerate harmless gut microbes and proteins from food. Scientists focused on a signal long believed to be essential for expanding immune cells that enforce tolerance. Instead, they found the opposite. Blocking this signal, rather than activating it, promoted tolerance in the intestine through a specific group of cells and significantly reduced inflammation in a preclinical model.<\/p>\n

A Paradigm-Shifting Discovery<\/p>\n

\u201cWe think this is a paradigm-shifting discovery that will lead to new treatment approaches for chronic inflammatory disorders of the intestine,\u201d said senior author Dr. Gregory Sonnenberg, the Henry R. Erle, M.D.-Roberts Family Professor of Medicine, associate vice chair of research in medicine, and a faculty member in the Division of Gastroenterology & Hepatology and the Jill Roberts Institute for Research in Inflammatory Bowel Disease at Weill Cornell Medicine.<\/p>\n

The study\u2019s lead and co-corresponding author, Dr. Mengze Lyu, is an instructor of microbiology and immunology in medicine and a member of the Sonnenberg Laboratory.<\/p>\n

\"Immune<\/a>Image visualizing immune cell aggregates in the intestine, demonstrating the presence of ROR\u03b3t+ APCs (red and green) and T cells (blue and red), whose interactions are critical in establishing immune tolerance in the intestine. Credit: Image provided by Dr. Gregory F. Sonnenberg.<\/p>\n

Scientists still do not fully understand how the immune system distinguishes harmful threats from harmless substances across different tissues. When this process fails, inappropriate immune responses can develop. This is especially common in the gut, where the body is constantly exposed to food molecules and microbes. Conditions such as Crohn\u2019s disease and ulcerative colitis affect millions of people in the United States.<\/p>\n

Unique Features of Gut Immunity<\/p>\n

The intestinal immune system relies on specialized local cells, which makes it particularly complex. Previous studies<\/a> have shown that immune tolerance in the gut is largely maintained by a subset of regulatory T cells known as Treg cells that express the transcription factor ROR\u03b3t.<\/p>\n

The Sonnenberg lab previously identified a unique group of antigen-presenting cells (APCs) that also express ROR\u03b3t. These cells are concentrated in the gut and are critical for maintaining immune balance. Further work by Drs. Lyu and Sonnenberg showed that gut ROR\u03b3t+ Treg cells depend<\/a> on direct signals from these APCs.<\/p>\n

In general, T cell activation follows a two-step process sometimes described as a \u201ctwo-factor authentication\u201d system. The first step, called Signal One, occurs when an APC presents a fragment of a molecule, known as an antigen, to a T cell.<\/p>\n

Rethinking the \u201cSecond Signal\u201d<\/p>\n

The new study focused on Signal Two, which typically involves receptor interactions between T cells and APCs and is required for T cell activation outside the gut.<\/p>\n

Unexpectedly, this second signal did not drive expansion of gut ROR\u03b3t+ Treg cells when combined with Signal One. Instead, blocking Signal Two while maintaining Signal One led to increased numbers of these cells and protected against intestinal inflammation in a preclinical model. This response is the opposite of what is seen in Treg cells outside the gut, highlighting the distinct nature of intestinal immunity.<\/p>\n

An existing drug, CTLA4-Ig, also known as abatacept, blocks the Signal Two interaction. Although it did not improve outcomes for IBD patients in a 2012 clinical report, the new findings help explain why. The researchers found that ROR\u03b3t+ APCs are reduced in people with IBD. Without these cells, the immune system cannot deliver the Signal One needed to support Treg cell expansion when Signal Two is blocked.<\/p>\n

\u201cOur results suggest that CTLA4-Ig could be effective against inflammatory bowel disease, if we could restore ROR\u03b3t+ APCs that are missing, or give CTLA4-Ig to patients who are in remission and still have these cells present and functional in the intestine,\u201d Dr. Lyu said.<\/p>\n

The team is now exploring these possibilities. Because ROR\u03b3t+ Treg cells also help protect against food allergies, side effects from cancer immunotherapy, and other chronic inflammatory conditions, researchers believe this approach could have broader applications for improving gut health.<\/p>\n

Reference: \u201cB7 costimulation antagonizes ROR\u03b3t+ regulatory T cells and immune tolerance in the intestine\u201d by Mengze Lyu and Gregory F. Sonnenberg, 24 April 2026, Journal of Experimental Medicine.
DOI: 10.1084\/jem.20251094<\/a><\/p>\n

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