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Probiotics modulate the gut microbiota composition and immune responses in patients with atopic dermatitis: a pilot study

机译:益生菌调节特应性皮炎患者的肠道微生物群组成和免疫应答:试验研究

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Purpose Many studies have investigated the association between intestinal barrier impairment and the onset of atopic dermatitis (AD). The gut microbiota is essential to maintain physiological homeostasis and immune regulation of host. Therefore, the objectives were to determine the effects of probiotics on the clinical symptoms, immune responses, and gut microbiota in AD patients. Methods 109 patients were randomly divided into 4 groups, including placebo group, oligosaccharides group,Bifidobacterium bifidumCCFM16 group, andLactobacillus plantarumCCFM8610 group. At the end of the experiment, serological indicators, SCORAD, and DLQI indices were assessed. V3-V4 region of the 16S ribosomal RNA gene was sequenced to evaluate changes in the gut microbiota. Linear discriminant analysis (LDA) effect size was used to uncover microbial biomarkers and PICRUSt (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States) was used to predict gene family abundances based on 16S information. Results The results demonstrated that CCFM8610 significantly decreased the SCORAD index, and increased the serum IL-10 levels. Supplement with CCFM8610 and CCFM16 significantly influenced the alpha diversity, increased the proportion ofBacteroidetes, and reduced the F/B ratio. CCFM8610 treatment downregulated the functional genes of gut microbiota involvingStaphylococcus aureusinfection and upregulated the steroid hormone biosynthesis. Conclusion The results indicated a positive correlation between decreased SCORAD index and CCFM8610 treatment, and that CCFM8610 regulated the immune responses in AD patients. CCFM8610 treatment influences the gut microbiota composition and functional changes. In conclusion,L. plantarumCCFM8610 exerts the strain-specific amelioration effects on patients with AD. Trial registration: ChiCTR1800015330 (Clinicaltrials.gov Identifier).
机译:目的,许多研究已经研究了肠道屏障障碍与特应性皮炎的发作(AD)之间的关联。肠道微生物生物是保持生理稳态和宿主免疫调节至关重要。因此,目的是确定益生菌对AD患者临床症状,免疫应答和肠道微生物的影响。方法将109名患者随机分为4组,包括安慰剂组,寡糖组,双歧杆菌Bifidumccfm16组,雄鹿杆菌植物杆菌CFM8610组。在实验结束时,评估了血清学指标,Scorad和DLQI指数。测序16S核糖体RNA基因的V3-V4区域以评估肠道微生物的变化。线性判别分析(LDA)效应大小用于揭示微生物生物标志物和屠杀(通过重建未观察状态的社区的Phylocy调查)用于根据16S信息预测基因家族丰富。结果结果表明,CCFM8610显着降低了Scorad指数,并增加了血清IL-10水平。 CCFM8610和CCFM16的补充显着影响了α多样性,增加了伯段的比例,降低了F / B比。 CCFM8610治疗下调了肠道微生物的功能基因,涉及过敏性的肠道菌,并上调类固醇激素生物合成。结论结果表明,下降指标和CCFM8610治疗之间的正相关,CCFM8610调节了AD患者的免疫应答。 CCFM8610治疗影响肠道微生物群组成和功能变化。总之,升。 Plantarumccfm8610对广告患者施加质量特异性改善效果。试用注册:CHICTR1800015330(ClinicalTrials.gov标识符)。

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