Jauregui-Amezaga Aranzazu, Smet Annemieke
Department of Gastroenterology and Hepatology, University Hospital Antwerp, 2650 Edegem, Belgium.
Laboratory of Experimental Medicine and Pediatrics (LEMP), Faculty of Medicine and Health Sciences, University of Antwerp, 2610 Wilrijk, Belgium.
J Clin Med. 2024 Aug 7;13(16):4622. doi: 10.3390/jcm13164622.
The management of patients with inflammatory bowel disease (IBD) aims to control inflammation through the use of immunosuppressive treatments that target various points in the inflammatory cascade. However, the efficacy of these therapies in the long term is limited, and they often are associated with severe side effects. Although the pathophysiology of the disease is not completely understood, IBD is regarded as a multifactorial disease that occurs due to an inappropriate immune response in genetically susceptible individuals. The gut microbiome is considered one of the main actors in the development of IBD. Gut dysbiosis, characterised by significant changes in the composition and functionality of the gut microbiota, often leads to a reduction in bacterial diversity and anti-inflammatory anaerobic bacteria. At the same time, bacteria with pro-inflammatory potential increase. Although changes in microbiome composition upon biological agent usage have been observed, their role as biomarkers is still unclear. While most studies on IBD focus on the intestinal bacterial population, recent studies have highlighted the importance of other microbial populations, such as viruses and fungi, in gut dysbiosis. In order to modulate the aberrant immune response in patients with IBD, researchers have developed therapies that target different players in the gut microbiome. These innovative approaches hold promise for the future of IBD treatment, although safety concerns are the main limitations, as their effects on humans remain unknown.
炎症性肠病(IBD)患者的管理旨在通过使用针对炎症级联反应中各个环节的免疫抑制疗法来控制炎症。然而,这些疗法的长期疗效有限,且常常伴有严重的副作用。尽管该疾病的病理生理学尚未完全明确,但IBD被认为是一种多因素疾病,在遗传易感性个体中因不适当的免疫反应而发生。肠道微生物群被认为是IBD发病过程中的主要因素之一。肠道生态失调,其特征是肠道微生物群的组成和功能发生显著变化,常导致细菌多样性和抗炎厌氧菌减少。与此同时,具有促炎潜力的细菌增加。尽管已观察到使用生物制剂后微生物群组成的变化,但其作为生物标志物的作用仍不清楚。虽然大多数关于IBD的研究集中在肠道细菌群体上,但最近的研究强调了其他微生物群体,如病毒和真菌,在肠道生态失调中的重要性。为了调节IBD患者异常的免疫反应,研究人员开发了针对肠道微生物群中不同参与者的疗法。这些创新方法为IBD治疗的未来带来了希望,尽管安全问题是主要限制因素,因为它们对人类的影响仍然未知。