Pointner Lisa, Bethanis Athanasios, Thaler Michael, Traidl-Hoffmann Claudia, Gilles Stefanie, Ferreira Fatima, Aglas Lorenz
Department of Biosciences, University of Salzburg, Hellbrunnerstraße. 34, 5020 Salzburg, Austria.
Chair and Institute of Environmental Medicine, UNIKA-T, Technical University of Munich and Helmholtz Zentrum München, Augsburg, Germany.
Clin Transl Allergy. 2020 Aug 31;10:36. doi: 10.1186/s13601-020-00341-y. eCollection 2020.
The mechanisms involved in the induction of allergic sensitization by pollen are not fully understood. Within the last few decades, findings from epidemiological and experimental studies support the notion that allergic sensitization is not only dependent on the genetics of the host and environmental factors, but also on intrinsic features of the allergenic source itself. In this review, we summarize the current concepts and newest advances in research focusing on the initial mechanisms inducing pollen sensitization. Pollen allergens are embedded in a complex and heterogeneous matrix composed of a myriad of bioactive molecules that are co-delivered during the allergic sensitization. Surprisingly, several purified allergens were shown to lack inherent sensitizing potential. Thus, growing evidence supports an essential role of pollen-derived components co-delivered with the allergens in the initiation of allergic sensitization. The pollen matrix, which is composed by intrinsic molecules ( proteins, metabolites, lipids, carbohydrates) and extrinsic compounds ( viruses, particles from air pollutants, pollen-linked microbiome), provide a specific context for the allergen and has been proposed as a determinant of Th2 polarization. In addition, the involvement of various pattern recognition receptors (PRRs), secreted alarmins, innate immune cells, and the dependency of DCs in driving pollen-induced Th2 inflammatory processes suggest that allergic sensitization to pollen most likely results from particular combinations of pollen-specific signals rather than from a common determinant of allergenicity. The exact identification and characterization of such pollen-derived Th2-polarizing molecules should provide mechanistic insights into Th2 polarization and pave the way for novel preventive and therapeutic strategies against pollen allergies.
花粉诱导过敏致敏的机制尚未完全明确。在过去几十年中,流行病学和实验研究结果支持这样一种观点,即过敏致敏不仅取决于宿主的遗传学和环境因素,还取决于变应原来源本身的内在特征。在本综述中,我们总结了目前关于诱导花粉致敏初始机制的概念和最新研究进展。花粉变应原嵌入在一个复杂且异质的基质中,该基质由无数生物活性分子组成,这些分子在过敏致敏过程中共同传递。令人惊讶的是,几种纯化的变应原显示缺乏内在致敏潜力。因此,越来越多的证据支持与变应原共同传递的花粉衍生成分在过敏致敏起始中起关键作用。花粉基质由内在分子(蛋白质、代谢产物、脂质、碳水化合物)和外在化合物(病毒、空气污染物颗粒、与花粉相关的微生物群)组成,为变应原提供了特定环境,并被认为是Th2极化的决定因素。此外,各种模式识别受体(PRR)、分泌性警戒素、固有免疫细胞的参与以及树突状细胞在驱动花粉诱导的Th2炎症过程中的依赖性表明,对花粉的过敏致敏很可能源于花粉特异性信号的特定组合,而非变应原性的共同决定因素。准确识别和表征此类花粉衍生的Th2极化分子应能为Th2极化提供机制性见解,并为针对花粉过敏的新型预防和治疗策略铺平道路。