Sputa-Grzegrzolka Patrycja, Socha-Banasiak Anna, Dziegiel Piotr, Kempisty Bartosz
Division of Anatomy, Department of Human Morphology and Embryology, Faculty of Medicine, Wroclaw Medical University, 50-368 Wroclaw, Poland.
Department of Gastroenterology, Allergology and Pediatrics, Polish Mother's Memorial Hospital-Research Institute, 93-338 Lodz, Poland.
Int J Mol Sci. 2025 Jun 16;26(12):5754. doi: 10.3390/ijms26125754.
Inflammatory bowel diseases (IBDs), including Crohn's disease (CD), ulcerative colitis (UC), and IBD-unclassified (IBD-U), are chronic inflammatory disorders of the gastrointestinal tract. Chronic inflammation in the course of IBD is an important initiating factor of fibrosis of the intestinal wall. Intestinal fibrosis is one of the most common and important complications of IBD and, due to the irreversibility of the process and the need for surgical treatment, currently poses a major clinical challenge. In this review, we presented in detail the process of intestinal wall fibrosis at the molecular, immunological, and clinical levels. We characterized the mediators, including transforming growth factor β (TGF-β), tumor necrosis factor-α (TNF-α), and others participating in this process. We also described the type 2 epithelial-mesenchymal transition (EMT) process closely associated with chronic inflammation, leading to excessive development of connective tissue in the intestinal wall in the course of IBD.
炎症性肠病(IBD),包括克罗恩病(CD)、溃疡性结肠炎(UC)和未分类的IBD(IBD-U),是胃肠道的慢性炎症性疾病。IBD病程中的慢性炎症是肠壁纤维化的重要起始因素。肠纤维化是IBD最常见且重要的并发症之一,由于该过程的不可逆性以及手术治疗的必要性,目前构成了一项重大的临床挑战。在本综述中,我们在分子、免疫和临床层面详细阐述了肠壁纤维化的过程。我们对参与该过程的介质进行了特征描述,包括转化生长因子β(TGF-β)、肿瘤坏死因子-α(TNF-α)等。我们还描述了与慢性炎症密切相关的2型上皮-间质转化(EMT)过程,该过程在IBD病程中导致肠壁结缔组织过度增生。