Piccioni Andrea, Spagnuolo Fabio, Candelli Marcello, Voza Antonio, Covino Marcello, Gasbarrini Antonio, Franceschi Francesco
Department of Emergency Medicine, Fondazione Policlinico Universitario Agostino Gemelli-IRCCS, 00168 Rome, Italy.
Faculty of Medicine and Surgery, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
J Clin Med. 2024 Oct 12;13(20):6082. doi: 10.3390/jcm13206082.
Sepsis is a complex clinical syndrome characterized by an uncontrolled inflammatory response to an infection that may result in septic shock and death. Recent research has revealed a crucial link between sepsis and alterations in the gut microbiota, showing that the microbiome could serve an essential function in its pathogenesis and prognosis. In sepsis, the gut microbiota undergoes significant dysbiosis, transitioning from a beneficial commensal flora to a predominance of pathobionts. This transformation can lead to a dysfunction of the intestinal barrier, compromising the host's immune response, which contributes to the severity of the disease. The gut microbiota is an intricate system of protozoa, fungi, bacteria, and viruses that are essential for maintaining immunity and metabolic balance. In sepsis, there is a reduction in microbial heterogeneity and a predominance of pathogenic bacteria, such as proteobacteria, which can exacerbate inflammation and negatively influence clinical outcomes. Microbial compounds, such as short-chain fatty acids (SCFAs), perform a crucial task in modulating the inflammatory response and maintaining intestinal barrier function. However, the role of other microbiota components, such as viruses and fungi, in sepsis remains unclear. Innovative therapeutic strategies aim to modulate the gut microbiota to improve the management of sepsis. These include selective digestive decontamination (SDD), probiotics, prebiotics, synbiotics, postbiotics, and fecal microbiota transplantation (FMT), all of which have shown potential, although variable, results. The future of sepsis management could benefit greatly from personalized treatment based on the microbiota. Rapid and easy-to-implement tests to assess microbiome profiles and metabolites associated with sepsis could revolutionize the disease's diagnosis and management. These approaches could not only improve patient prognosis but also reduce dependence on antibiotic therapies and promote more targeted and sustainable treatment strategies. Nevertheless, there is still limited clarity regarding the ideal composition of the microbiota, which should be further characterized in the near future. Similarly, the benefits of therapeutic approaches should be validated through additional studies.
脓毒症是一种复杂的临床综合征,其特征是对感染产生不受控制的炎症反应,可能导致感染性休克和死亡。最近的研究揭示了脓毒症与肠道微生物群改变之间的关键联系,表明微生物群在其发病机制和预后中可能发挥重要作用。在脓毒症中,肠道微生物群会发生显著的生态失调,从有益的共生菌群转变为以致病共生菌为主。这种转变会导致肠道屏障功能障碍,损害宿主的免疫反应,从而加重疾病的严重程度。肠道微生物群是由原生动物、真菌、细菌和病毒组成的复杂系统,对维持免疫和代谢平衡至关重要。在脓毒症中,微生物异质性降低,以变形菌等致病菌为主,这会加剧炎症并对临床结果产生负面影响。微生物化合物,如短链脂肪酸(SCFAs),在调节炎症反应和维持肠道屏障功能方面发挥着关键作用。然而,其他微生物群成分,如病毒和真菌,在脓毒症中的作用仍不清楚。创新的治疗策略旨在调节肠道微生物群,以改善脓毒症的治疗。这些策略包括选择性消化道去污(SDD)、益生菌、益生元、合生元、后生元以及粪便微生物群移植(FMT),尽管结果各不相同,但所有这些都显示出了潜力。脓毒症治疗的未来可能会从基于微生物群的个性化治疗中受益匪浅。快速且易于实施的测试来评估与脓毒症相关的微生物群谱和代谢产物,可能会彻底改变该疾病的诊断和治疗。这些方法不仅可以改善患者的预后,还可以减少对抗生素治疗的依赖,并促进更具针对性和可持续性的治疗策略。然而,关于微生物群的理想组成仍存在有限的清晰度,这在不久的将来应进一步明确。同样,治疗方法的益处应通过更多研究来验证。
J Clin Med. 2024-10-12
Burns Trauma. 2023-6-15
World J Clin Cases. 2024-1-6
Front Cell Infect Microbiol. 2024
Therap Adv Gastroenterol. 2022-11-18
Autoimmun Rev. 2023-5
Front Immunol. 2018-9-10
Front Microbiol. 2025-6-26
Food Sci Nutr. 2025-6-8
Chin Med J (Engl). 2025-7-5
Front Microbiol. 2025-4-30
Front Psychiatry. 2024-3-28
Lancet Gastroenterol Hepatol. 2024-5
Microorganisms. 2024-2-25
Burns Trauma. 2023-6-15