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首页> 外文期刊>Allergy >Bet v 1 and its homologous food allergen Api g 1 stimulate dendritic cells from birch pollen-allergic individuals to induce different Th-cell polarization.
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Bet v 1 and its homologous food allergen Api g 1 stimulate dendritic cells from birch pollen-allergic individuals to induce different Th-cell polarization.

机译:Bet v 1及其同源食物过敏原Api g 1刺激桦树花粉过敏个体的树突状细胞诱导不同的Th细胞极化。

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摘要

BACKGROUND: Bet v 1 is the most relevant sensitizing protein for birch pollen (BP)-allergic individuals. Its homologues from plant foods are mainly involved in allergic reactions caused by IgE cross reactivity. We aimed to evaluate the polarizing effect of dendritic cells (DCs) pulsed with Bet v 1, Mal d 1, Api g 1 or Dau c 1 on Th-cell responses. METHODS: Immature DCs were generated from peripheral blood monocytes of BP-allergic and healthy donors by culture with GM-CSF and IL-4 and subsequently pulsed with allergens in combination with maturation factors. Cell surface markers were analysed by FACS. Mature DCs were co-cultured with autologous Th cells and T-cell proliferation and cytokine profiles were determined. RESULTS: In co-culture, mature allergen-pulsed DCs induced autologous Th cells of BP-allergic donors to proliferate significantly more than those of healthy individuals. Exposure of DCs from BP-allergic donors to Bet v 1 resulted in a robust Th2 skewing with significantly higher quantities of IL-5 and elevated IL-13 compared to maturation factors. In contrast, Api g 1-primed DCs from BP allergics significantly enhanced the production of the Th1 cytokine IFN-gamma and significantly down-regulated IL-13 compared to maturation factors. In healthy donors, no significant cytokine production could be detected. CONCLUSION: Bet v 1 in contrast to homologous food allergens seems to possess distinct molecular features that enable it to condition DCs from BP-allergic donors to induce allergen-specific T-cell proliferation and Th2 polarization.
机译:背景:Bet v 1是桦木花粉(BP)过敏性个体最相关的致敏蛋白。它来自植物食品的同源物主要参与由IgE交叉反应性引起的过敏反应。我们旨在评估用Bet v 1,Mal d 1,Api g 1或Dau c 1脉冲处理的树突状细胞(DC)对Th细胞反应的极化作用。方法:通过与GM-CSF和IL-4的培养,从BP过敏和健康供体的外周血单核细胞中生成未成熟的DC,然后用变应原与成熟因子结合进行脉冲处理。通过FACS分析细胞表面标记。将成熟的DC与自体Th细胞共培养,并测定T细胞增殖和细胞因子谱。结果:在共培养物中,成熟的变应原脉冲DCs诱导BP过敏性供体的自体Th细胞比健康个体的自体Th细胞增殖得多。与成熟因子相比,将来自BP过敏性供体的DC暴露于Bet v 1导致了牢固的Th2偏斜,其中IL-5的量显着更高,IL-13的升高。相比之下,与成熟因子相比,来自BP过敏症的Api g 1引发的DC显着增强了Th1细胞因子IFN-γ的产生,并显着下调了IL-13。在健康的供体中,未检测到明显的细胞因子产生。结论:与同源食物过敏原相比,Bet v 1似乎具有独特的分子特征,使其能够调节来自BP过敏性供体的DC,以诱导过敏原特异性T细胞增殖和Th2极化。

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