October 9, 2019

This article has been reviewed according to Science X's editorial process and policies. Editors have highlighted the following attributes while ensuring the content's credibility:

Blood vessels offer new approaches for treating chronic inflammatory bowel diseases

In chronic inflammatory bowel diseases, fluid (yellow and red) seeps from the blood vessels into the interjacent indentations in the bowel wall (green, image 1). Blood vessels that do not react to interferon-γ remain impermeable under these conditions (image 2). Credit: Universitätsklinikum Erlangen
× close
In chronic inflammatory bowel diseases, fluid (yellow and red) seeps from the blood vessels into the interjacent indentations in the bowel wall (green, image 1). Blood vessels that do not react to interferon-γ remain impermeable under these conditions (image 2). Credit: Universitätsklinikum Erlangen

In Germany alone, there are around 400,000 patients who suffer from chronic inflammatory bowel diseases. For the first time, researchers at Universitätsklinikum Erlangen have discovered that dysfunctions in blood vessels play a significant role in the development of such diseases. In experimental model systems, the progression of the disease slowed down significantly by eliminating these dysfunctions. The researchers have now published their results in the Journal of Clinical Investigation.

Diseases in humans are often caused by malfunctioning cells. Epithelium cells, which form the barrier between the bowel and surrounding tissue, and have been the focus of investigations of the mechanisms of chronic inflammatory diseases of the bowel. While it is well known that inflammatory cells can only reach the relevant tissue via blood vessels, the role of blood vessels in chronic inflammatory bowel diseases has not been very well researched. A group of researchers in molecular and experimental surgery at the Department of Surgery and interdisciplinary collaborators have now conducted an in-depth investigation of the role of blood vessels.

Highly permeable blood vessels

The interdisciplinary cooperation project, which was primarily implemented by Victoria Langer as part of her doctoral thesis, discovered that the blood vessels of patients with chronic inflammatory bowel disease are especially permeable. In molecular analyses, the researchers identified the cause as a malfunction in the cell-to-cell interaction in endothelial cells. Endothelial cells form the lining of blood vessels and are responsible for maintaining vessel wall impermeability. The dysfunction is caused by a specific cytokine known as interferon-γ, which is present in higher concentrations in chronically inflamed intestinal tissue. The increased permeability of was proven in various experimental models and in patients with chronic inflammatory bowel diseases.

The significance of vessel permeability was demonstrated using genetic methods in experiments in animal models, as the ability of to react to interferon-γ was inhibited, which significantly slowed down the progression of the disease. A significant clinical finding is that the drug Imatinib (Glivec), also inhibits permeability, significantly suppressing progression. Imatinib (Glivec) is currently used to treat cancer.

The study proves for the first time the great significance of the cardiovascular system in chronic inflammatory bowel diseases and opens up new approaches for treatments. Prof. Michael Stürzl started researching chronic inflammatory diseases only a few years ago. He says, "We really hope, of course, that our results will benefit patients with chronic inflammatory bowel diseases in the long term. This is also being supported by the fact that the medication we successfully used in the has already been approved for clinical applications."

More information: Victoria Langer et al. IFN-γ drives inflammatory bowel disease pathogenesis through VE-cadherin–directed vascular barrier disruption, Journal of Clinical Investigation (2019). DOI: 10.1172/JCI124884

Journal information: Journal of Clinical Investigation

Load comments (0)