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Contribution of Blood Vessel Activation, Remodeling and Barrier Function to Inflammatory Bowel Diseases

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MDPI
DOI: 10.3390/ijms24065517

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inflammatory bowel diseases (IBDs); vasculature; angiogenesis; gut vascular barrier; vessel permeability

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Inflammatory bowel diseases (IBDs) are chronic inflammatory disorders with a complex etiology that are often difficult to treat. In IBD, inflammation of the intestinal mucosa is characterized by strong and sustained leukocyte infiltration, leading to barrier dysfunction and tissue destruction. The role of the gut vasculature in promoting inflammation is increasingly recognized.
Inflammatory bowel diseases (IBDs) consist of a group of chronic inflammatory disorders with a complex etiology, which represent a clinical challenge due to their often therapy-refractory nature. In IBD, inflammation of the intestinal mucosa is characterized by strong and sustained leukocyte infiltration, resulting in the loss of epithelial barrier function and subsequent tissue destruction. This is accompanied by the activation and the massive remodeling of mucosal micro-vessels. The role of the gut vasculature in the induction and perpetuation of mucosal inflammation is receiving increasing recognition. While the vascular barrier is considered to offer protection against bacterial translocation and sepsis after the breakdown of the epithelial barrier, endothelium activation and angiogenesis are thought to promote inflammation. The present review examines the respective pathological contributions of the different phenotypical changes observed in the microvascular endothelium during IBD, and provides an overview of potential vessel-specific targeted therapy options for the treatment of IBD.

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