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Allergen recognition by innate immune cells: critical role of dendritic and epithelial cells

机译:先天免疫细胞对过敏原的识别:树突状细胞和上皮细胞的关键作用

摘要

Allergy is an exacerbated response of the immune system against non-self-proteins called allergens and is typically characterized by biased type-2 T helper cell and deleterious IgE mediated immune responses. The allergic cascade starts with the recognition of allergens by antigen presenting cells, mainly dendritic cells (DCs), leading to Th2 polarization, switching to IgE production by B cells, culminating in mast cell sensitization and triggering. DCs have been demonstrated to play a crucial role in orchestrating allergic diseases. Using different C-type lectin receptors DCs are able to recognize and internalize a number of allergens from diverse sources leading to sensitization. Furthermore, there is increasing evidence highlighting the role of epithelial cells in triggering and modulating immune responses to allergens. As well as providing a physical barrier, epithelial cells can interact with allergens and influence DCs behavior through the release of a number of Th2 promoting cytokines. In this review we will summarize current understanding of how allergens are recognized by DCs and epithelial cells and what are the consequences of such interaction in the context of allergic sensitization and downstream events leading to allergic inflammation. Better understanding of the molecular mechanisms of allergen recognition and associated signaling pathways could enable developing more effective therapeutic strategies that target the initial steps of allergic sensitization hence hindering development or progression of allergic diseases.
机译:变态反应是免疫系统对称为变应原的非自身蛋白的反应加剧,通常以2型T辅助细胞偏向和有害IgE介导的免疫反应为特征。过敏级联反应首先是由抗原呈递细胞(主要是树突状细胞(DC))识别过敏原,导致Th2极化,由B细胞转换为IgE产生,最终导致肥大细胞致敏并触发。 DC已被证明在协调过敏性疾病中起关键作用。使用不同的C型凝集素受体,DC能够识别并内化来自多种来源的多种过敏原,从而导致过敏。此外,越来越多的证据突出了上皮细胞在触发和调节对过敏原的免疫反应中的作用。上皮细胞除了提供物理屏障外,还可以与过敏原相互作用,并通过释放多种促进Th2的细胞因子来影响DC的行为。在这篇综述中,我们将总结目前对DC和上皮细胞如何识别过敏原的理解,以及在过敏性致敏和导致过敏性炎症的下游事件中这种相互作用的后果。对变应原识别和相关信号传导途径的分子机制的更好理解可以使开发针对变应性致敏的初始步骤的更有效的治疗策略,从而阻碍变应性疾病的发展或发展。

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