Division of Clinical and Molecular Allergology, Research Center Borstel, Leibniz Lung Center, Airway Research Center North, German Center for Lung Research, Borstel, Germany.
Interdisciplinary Allergy Outpatient Clinic, Department of Pneumology, University of Luebeck, Borstel, Germany.
Front Immunol. 2019 Feb 14;10:122. doi: 10.3389/fimmu.2019.00122. eCollection 2019.
Molecular allergology research has provided valuable information on the structure and function of single allergenic molecules. There are several allergens in food and inhalant allergen sources that are able to interact with lipid ligands different structural features: hydrophobic pockets, hydrophobic cavities, or specialized domains. For only a few of these allergens information on their associated ligands is already available. Several of the allergens are clinically relevant, so that it is highly probable that the individual structural features with which they interact with lipids have a direct effect on their allergenic potential, and thus on allergy development. There is some evidence for a protective effect of lipids delaying the enzymatic digestion of the peanut () allergen Ara h 8 (hydrophobic pocket), probably allowing this molecule to get to the intestinal immune system intact (sensitization). Oleosins from different food allergen sources are part of lipid storage organelles and potential marker allergens for the severity of the allergic reaction. House dust mite (HDM), is more often associated with allergic asthma than other sources of inhalant allergens. In particular, lipid-associated allergens from which are Der p 2, Der p 5, Der p 7, Der p 13, Der p 14, and Der p 21 have been reported to be associated with severe allergic reactions and respiratory symptoms such as asthma. The exact mechanism of interaction of these allergens with lipids still has to be elucidated. Apart from single allergens glycolipids have been shown to directly induce allergic inflammation. Several-in parts conflicting-data exist on the lipid (and allergen) and toll-like receptor interactions. For only few single allergens mechanistic studies were performed on their interaction with the air-liquid interface of the lungs, in particular with the surfactant components SP-A and SP-D. The increasing knowledge on protein-lipid-interaction for lipophilic and hydrophobic food and inhalant allergens on the basis of their particular structure, of their capacity to be integral part of membranes (like the oleosins), and their ability to interact with membranes, surfactant components, and transport lipids (like the lipid transfer proteins) are essential to eventually clarify allergy and asthma development.
分子过敏学研究为单一过敏原分子的结构和功能提供了有价值的信息。食物和吸入性过敏原来源中有几种过敏原能够与不同结构特征的脂质配体相互作用:疏水口袋、疏水腔或特化结构域。只有少数几种过敏原的相关配体信息是可用的。其中一些过敏原具有临床相关性,因此它们与脂质相互作用的特定结构特征极有可能直接影响其致敏潜能,从而影响过敏的发展。有一些证据表明,脂质具有保护作用,可以延迟花生()过敏原 Ara h 8(疏水口袋)的酶解,可能使这种分子完整地进入肠道免疫系统(致敏)。不同食物过敏原来源的油脂蛋白是脂质储存细胞器的一部分,也是过敏反应严重程度的潜在标志物过敏原。屋尘螨(HDM)比其他吸入性过敏原更常与过敏性哮喘相关。特别是,与严重过敏反应和呼吸道症状(如哮喘)相关的脂质相关过敏原包括 Der p 2、Der p 5、Der p 7、Der p 13、Der p 14 和 Der p 21。这些过敏原与脂质相互作用的确切机制仍有待阐明。除了单一过敏原外,糖脂也被证明可以直接诱导过敏炎症。关于脂质(和过敏原)与 Toll 样受体相互作用的部分存在相互矛盾的数据。只有少数几种单一过敏原的相互作用机制研究是在它们与肺部气液界面的相互作用,特别是与表面活性剂成分 SP-A 和 SP-D 的相互作用方面进行的。基于其特定结构、作为膜的完整部分的能力(如油脂蛋白)以及与膜、表面活性剂成分和转运脂质相互作用的能力,对亲脂性和疏水性食物和吸入性过敏原的蛋白质-脂质相互作用的认识不断增加,对于最终阐明过敏和哮喘的发展至关重要。