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Characterization of candidate anti-allergic probiotic strains in a model of Th2-skewed human peripheral blood mononuclear cells

机译:Th2偏向人外周血单核细胞模型中候选抗过敏益生菌菌株的表征

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Background: Pre-clinical and clinical studies have evaluated the efficacy of probiotics in allergy. However, predictive in vitro systems for rational strain selection are still missing. Methods: We developed a novel in vitro screening system for the characterization of probiotics with anti-allergic potential. In this model, human peripheral blood mononuclear cells (PBMC) from healthy donors (n = 68) were skewed towards a Th2 cytokine phenotype by culture with IL-4 and anti-CD40, to resemble cells from allergic donors. Th2-skewed cells were then co-cultured with probiotics; a total of 35 strains were tested. Levels of IFN-γ, IL-10, IL-5 and 7 additional cytokines in culture supernatants were determined by ELISA or multiplex assay. Gene expression was assessed by real-time PCR. For validation, splenocytes from ovalbumin-primed mice and PBMC from grass-allergic donors were restimulated with respective antigen and co-cultured with probiotics, and cytokine profiles were correlated. Results: Culture with IL-4 and anti-CD40 antibody induced secretion of IL-5 from PBMC, indicative of induction of a Th2 phenotype. Cytokine profiles induced by probiotics were strain specific even though species- and genus-specific clustering was observed for many strains by principal component analysis. This was paralleled by mRNA levels of the corresponding genes such as increased Tbet and reduced GATA-3 gene expression. Cytokine profiles induced by probiotics in PBMC stimulated with IL-4 and anti-CD40 correlated with those obtained from allergen-stimulated murine splenocytes or human PBMC from grass-allergic donors. Conclusions: Cytokine profiling of probiotic strains with IL-4-/anti-CD40- stimulated PBMC allowed to determine the effect of probiotics on Th2-skewed cells and thus to classify probiotic strains with anti-allergic potential.
机译:背景:临床前和临床研究已经评估了益生菌对过敏的功效。但是,仍然缺少用于合理菌株选择的预测性体外系统。方法:我们开发了一种新型的体外筛选系统,用于表征具有抗过敏潜力的益生菌。在该模型中,健康供体(n = 68)的人外周血单核细胞(PBMC)通过与IL-4和抗CD40的培养而偏向Th2细胞因子表型,类似于过敏性供体的细胞。然后将Th2偏斜的细胞与益生菌共培养;总共测试了35个菌株。培养上清液中的IFN-γ,IL-10,IL-5和7种其他细胞因子的水平通过ELISA或多重分析确定。通过实时PCR评估基因表达。为了进行验证,卵清蛋白引发小鼠的脾细胞和草过敏性供体的PBMC分别用各自的抗原再刺激,并与益生菌共培养,并关联细胞因子谱。结果:与IL-4和抗CD40抗体一起培养可诱导PBMC分泌IL-5,这表明可诱导Th2表型。益生菌诱导的细胞因子谱是菌株特异性的,即使通过主成分分析对许多菌株观察到物种和属特异性的聚类也是如此。与此相对应的是相应基因的mRNA水平,例如Tbet升高和GATA-3基因表达降低。益生菌在IL-4和抗CD40刺激下在PBMC中诱导的细胞因子谱与从变应原刺激的鼠脾细胞或人PBMC中从草过敏性供体获得的那些相关。结论:用IL-4- /抗CD40刺激的PBMC对益生菌菌株进行细胞因子谱分析,可以确定益生菌对Th2偏斜细胞的作用,从而可以对具有抗过敏潜力的益生菌菌株进行分类。

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