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变应原诱导的白细胞介素-6调节变应性气道炎症中CD4+ T细胞的白细胞介素-9/白细胞介素-17A平衡。

Allergen-Induced IL-6 Regulates IL-9/IL-17A Balance in CD4+ T Cells in Allergic Airway Inflammation.

作者信息

Schütze Nicole, Trojandt Stefanie, Kuhn Stephanie, Tomm Janina M, von Bergen Martin, Simon Jan C, Polte Tobias

机构信息

Leipzig Research Center for Civilization Diseases, Junior Research Group on Pathogenesis of New Allergies, Leipzig University Medical Center, 04103 Leipzig, Germany; Department of Dermatology, Venerology and Allergology, Leipzig University Medical Center, 04103 Leipzig, Germany;

Department of Environmental Immunology, UFZ-Helmholtz Center for Environmental Research, 04318 Leipzig, Germany;

出版信息

J Immunol. 2016 Oct 1;197(7):2653-64. doi: 10.4049/jimmunol.1501599. Epub 2016 Aug 29.

Abstract

IL-9-secreting Th9 cells have been considered to play a pivotal role in the pathogenesis of atopic diseases. To what extent IL-9-producing cells are induced or regulated by sensitization with naturally occurring allergens is not yet clear. Naturally occurring allergens are capable of inducing IL-6 production in dendritic cells (DCs). Whether allergen-induced IL-6 supports a Th9 subtype by increasing IL-9 production, as observed in in vitro studies, or rather favors Th17 differentiation is not finally resolved. Therefore, in the present study we have investigated the impact of IL-6 on the Th9/Th17 balance depending on the predominant cytokine milieu and, additionally, in vivo using a DC-driven murine asthma model. In vitro, IL-6 increases Th9 cells under strong IL-4 and TGF-β activation, whereas under moderate IL-4 and TGF-β activation the presence of IL-6 shifts naive CD4(+) cells to Th17 cells. To induce allergic airway inflammation, OVA-pulsed DCs from IL-6-deficient or wild-type donors were adoptively transferred into BALB/c mice. Recipients receiving IL-6-producing wild-type DCs showed a significant decrease of Th9- and IL-4-producing Th2 cells but an increase of Th17 cells in lung tissue in comparison with recipients sensitized with IL-6-deficient DCs. Our data suggest that the IL-6-mediated reduction of Th2-related IL-4 leads to a decline of the Th9 immune response and allows Th17 differentiation.

摘要

分泌白细胞介素-9(IL-9)的Th9细胞被认为在特应性疾病的发病机制中起关键作用。天然存在的过敏原致敏诱导或调节产生IL-9细胞的程度尚不清楚。天然存在的过敏原能够诱导树突状细胞(DCs)产生IL-6。过敏原诱导的IL-6是否如体外研究所观察到的那样通过增加IL-9的产生来支持Th9亚型,还是更有利于Th17分化,目前尚未最终解决。因此,在本研究中,我们研究了IL-6对Th9/Th17平衡的影响,这取决于主要的细胞因子环境,此外,还在体内使用DC驱动的小鼠哮喘模型进行了研究。在体外,在强IL-4和转化生长因子-β(TGF-β)激活下,IL-6增加Th9细胞,而在中度IL-4和TGF-β激活下,IL-6的存在将初始CD4(+)细胞转变为Th17细胞。为了诱导过敏性气道炎症,将来自IL-6缺陷或野生型供体的卵清蛋白(OVA)脉冲DC过继转移到BALB/c小鼠体内。与用IL-6缺陷DC致敏的受体相比,接受产生IL-6的野生型DC的受体在肺组织中Th9和产生IL-4的Th2细胞显著减少,但Th17细胞增加。我们的数据表明,IL-6介导的Th2相关IL-4的减少导致Th9免疫反应下降,并允许Th17分化。

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