Misselwitz Benjamin, Haller Dirk
Medizinische Klinik und Poliklinik II, Ludwig-Maximilians-Universität München, Marchioninistraße 15, 83477, München, Deutschland.
Lehrstuhl für Ernährung und Immunologie, School of Life Sciences, Technische Universität München, Gregor-Mendel-Straße 2, 85354, Freising, Deutschland.
Inn Med (Heidelb). 2025 Feb;66(2):146-155. doi: 10.1007/s00108-024-01845-6. Epub 2025 Jan 27.
The intestinal microbiota comprises all living microorganisms in the gastrointestinal tract and is crucial for its function. Clinical observations and laboratory findings confirm a central role of the microbiota in chronic inflammatory bowel diseases (IBD). However, many mechanistic details remain unclear.
Changes in the microbiota and the causal relationship with the pathogenesis of IBD are described and current and future diagnostic and therapeutic options are discussed.
Narrative review.
The intestinal microbiota is altered in composition, diversity, and function in IBD patients, but specific (universal) IBD-defining bacteria have not been identified. The healthy microbiota has numerous anti-inflammatory functions such as the production of short-chain fatty acids or competition with pathogens. In contrast, the IBD microbiota promotes inflammation through the destruction of the intestinal barrier and direct interaction with the immune system. The balance between pro- and anti-inflammatory effects of the microbiota appears to be crucial for the development of intestinal inflammation. Microbiota-based IBD diagnostics show promise but are not yet ready for clinical use. Probiotics and fecal microbiota transplantation have clinical effects, especially in ulcerative colitis, but the potential of microbiota-based therapies is far from being fully realized.
IBD dysbiosis remains undefined so far. It is unclear how the many parallel pro- and anti-inflammatory mechanisms contribute to IBD pathogenesis. An inadequate mechanistic understanding hinders the development of microbiota-based diagnostics and therapies.
肠道微生物群包括胃肠道中的所有活微生物,对其功能至关重要。临床观察和实验室研究结果证实微生物群在慢性炎症性肠病(IBD)中起核心作用。然而,许多机制细节仍不清楚。
描述微生物群的变化及其与IBD发病机制的因果关系,并讨论当前和未来的诊断及治疗选择。
叙述性综述。
IBD患者的肠道微生物群在组成、多样性和功能方面发生改变,但尚未确定特定的(通用的)定义IBD的细菌。健康的微生物群具有多种抗炎功能,如产生短链脂肪酸或与病原体竞争。相比之下,IBD微生物群通过破坏肠道屏障和与免疫系统直接相互作用来促进炎症。微生物群促炎和抗炎作用之间的平衡似乎对肠道炎症的发展至关重要。基于微生物群的IBD诊断显示出前景,但尚未准备好用于临床。益生菌和粪便微生物群移植具有临床效果,尤其是在溃疡性结肠炎中,但基于微生物群的治疗潜力远未得到充分实现。
迄今为止,IBD生态失调仍未明确。目前尚不清楚众多平行的促炎和抗炎机制如何导致IBD发病。对机制的理解不足阻碍了基于微生物群的诊断和治疗的发展。