肠道细菌和溃疡性结肠炎。

J H Cummings, G T Macfarlane, S Macfarlane
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摘要

来自动物模型和溃疡性结肠炎(UC)患者研究的令人信服的证据表明,肠道微生物群参与了这种情况下炎症过程的启动和维持。尽管如此,还没有确定特定的病原体是致病的,人们普遍认为这种疾病是由基因决定的,但对共生细菌的异常免疫反应引起的。与健康人相比,UC患者的黏膜IgG水平升高,直接针对正常的微生物群。UC粘膜细菌群的研究表明,微生物数量可能增加,但“保护性”细菌(如乳酸杆菌和双歧杆菌)的数量减少。在结肠炎的动物模型中,抗生素,特别是甲硝唑、克林霉素、环丙沙星和万古霉素/亚米嫩联合用药可以预防UC,特别是在炎症发生之前。这些抗生素针对厌氧菌和一些革兰氏阳性菌,如肠球菌。然而,在十多个随机对照试验中,抗生素的使用情况非常令人失望,可能是因为我们不知道应该针对哪些物种,何时使用抗生素,使用多长时间以及以何种组合使用。因此,令人惊讶的是,在少数研究报告中,益生菌对UC和袋炎的治疗有一致的益处。在这一领域还有更多的工作要做,重点是粘膜微生物群,它与肠道免疫系统的相互作用,它的代谢特性以及改变它的潜在方法。
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Intestinal bacteria and ulcerative colitis.

Convincing evidence from both animal models and the study of patients with ulcerative colitis (UC) implicates the intestinal microflora in the initiation and maintenance of the inflammatory processes in this condition. Despite this, no specific pathogen has been identified as causal and the disease is widely believed to occur as the result of a genetically determined, but abnormal immune response to commensal bacteria. When compared with healthy people, UC patients have increased levels of mucosal IgG directed against the normal microflora. Studies of mucosal bacterial populations in UC indicate that there may be increased numbers of organisms, but reduced counts of "protective" bacteria such as lactobacilli and bifidobacteria. In animal models of colitis, antibiotics, particularly metronidazole, clindamycin, ciprofloxacin and the combination of vancomycin/impinemem protect against UC, especially if given before the onset of inflammation. These antibiotics target anaerobes and some Gram-positive organisms such as enterococci. However, antibiotic use in more than a dozen randomised control trials has been very disappointing, probably because we do not know which species to target, when to give the antibiotics, for how long and in what combinations. Surprisingly, therefore, there is a consistent benefit in the small number of studies reported of probiotics to manage UC and pouchitis. There is scope for more work in this area focussing on the mucosal microflora, its interactions with the gut immune system, its metabolic properties and the potential ways of modifying it.

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Molecular interactions between bacteria, the epithelium, and the mucosal immune system in the intestinal tract: implications for chronic inflammation. Taxonomy of Lactobacilli and Bifidobacteria. Effect of the probiotic Enterococcus faecium NCIMB10415 on cell numbers of total Enterococcus spp., E. faecium and E. faecalis in the intestine of piglets. Differences between the fecal microbiota of coeliac infants and healthy controls. Applications of bacteriocins in livestock.
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