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Microbiome in atopic dermatitis

机译:特应性皮炎中的微生物组

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Atopic dermatitis (AD) is a common chronic inflammatory skin disease affecting ~10–20% of the general population. AD is characterized by disturbances in epidermal barrier function and hyperactive immune response. Recently, changes in the skin and intestinal microbiome have been analyzed in more detail. The available data suggest a link between disturbed skin microbiome and course of the disease. Flares of the disease are associated with an expansion of Staphylococcus aureus on lesional skin and a substantial loss of biodiversity in skin microbiome. Staphylococci exoproteins and superantigens evoke inflammatory reactions in the host. Skin microbiome includes superficial stratum corneum that is affected by environmental factors such as exposure to germs and cleansing. Available evidence argues for a link between epidermal barrier impairment and disturbances in skin microbiome in AD. In contrast to skin microbiome, intestinal microbiome seems to become stabilized after infancy. There is also a significant heritable component for intestinal microbiome. The microbial taxa, relative percentages and quantities vary remarkably between the different parts of the intestinal tract. Early intestinal microbial colonization may be a critical step for prevention of further development of AD. Skin barrier-aimed topical treatments help to develop a neo-microbiome from deeper compartments. Probiotics, prebiotics and synbiotics have been investigated for the treatment of AD, but further investigations are needed. Targeted treatment options to normalize skin and intestinal microbiome in AD are under investigation.
机译:特应性皮炎(AD)是一种常见的慢性炎症性皮肤病,约占总人口的10–20%。 AD的特征在于表皮屏障功能和免疫反应过度活跃。最近,已经对皮肤和肠道微生物组的变化进行了更详细的分析。现有数据表明皮肤微生物组紊乱与病程之间存在联系。该疾病的发作与病灶皮肤上的金黄色葡萄球菌扩张以及皮肤微生物组中生物多样性的大量丧失有关。葡萄球菌外蛋白和超抗原在宿主中引起炎症反应。皮肤微生物组包括受环境因素(例如接触细菌和清洁)影响的表皮角质层。现有证据表明,AD中表皮屏障障碍与皮肤微生物组紊乱之间存在联系。与皮肤微生物组相反,婴儿后肠道微生物组似乎变得稳定。肠道微生物组还有一个重要的可遗传成分。肠道不同部分之间的微生物分类群,相对百分比和数量显着不同。早期肠道微生物定植可能是预防AD进一步发展的关键步骤。针对皮肤屏障的局部治疗有助于从更深的隔室中形成新的微生物组。已经研究了益生菌,益生元和合生元用于AD的治疗,但还需要进一步研究。正在研究使AD中的皮肤和肠道微生物组正常化的靶向治疗方案。

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