Research and Development Department, IMG Pharma Biotech S.L., 48170 Zamudio, Spain.
Department of Immunology, Microbiology and Parasitology, Faculty of Science and Technology, University of the Basque Country (UPV/EHU), 48940 Leioa, Spain.
Int J Mol Sci. 2024 Jun 27;25(13):7062. doi: 10.3390/ijms25137062.
In inflammatory bowel diseases (IBDs), such as Crohn's disease (CD) and ulcerative colitis (UC), the immune system relentlessly attacks intestinal cells, causing recurrent tissue damage over the lifetime of patients. The etiology of IBD is complex and multifactorial, involving environmental, microbiota, genetic, and immunological factors that alter the molecular basis of the organism. Among these, the microbiota and immune cells play pivotal roles; the microbiota generates antigens recognized by immune cells and antibodies, while autoantibodies target and attack the intestinal membrane, exacerbating inflammation and tissue damage. Given the altered molecular framework, the analysis of multiple molecular biomarkers in patients proves exceedingly valuable for diagnosing and prognosing IBD, including markers like C reactive protein and fecal calprotectin. Upon detection and classification of patients, specific treatments are administered, ranging from conventional drugs to new biological therapies, such as antibodies to neutralize inflammatory molecules like tumor necrosis factor (TNF) and integrin. This review delves into the molecular basis and targets, biomarkers, treatment options, monitoring techniques, and, ultimately, current challenges in IBD management.
在炎症性肠病 (IBD) 中,如克罗恩病 (CD) 和溃疡性结肠炎 (UC),免疫系统无情地攻击肠道细胞,导致患者终生反复发生组织损伤。IBD 的病因复杂且多因素,涉及环境、微生物群、遗传和免疫因素,这些因素改变了机体的分子基础。在这些因素中,微生物群和免疫细胞起着关键作用;微生物群产生被免疫细胞和抗体识别的抗原,而自身抗体则针对并攻击肠道膜,加剧炎症和组织损伤。鉴于改变了的分子框架,对患者的多个分子生物标志物进行分析对于诊断和预测 IBD 非常有价值,包括 C 反应蛋白和粪便钙卫蛋白等标志物。在检测和分类患者后,会给予特定的治疗,包括传统药物和新型生物疗法,例如针对肿瘤坏死因子 (TNF) 和整合素等炎症分子的抗体。本文深入探讨了 IBD 管理中的分子基础和靶点、生物标志物、治疗选择、监测技术以及最终的当前挑战。