Christian Doppler Laboratory for Allergy Diagnosis and Therapy, University of Salzburg, Salzburg, Austria.
Clin Exp Allergy. 2014 Mar;44(3):438-49. doi: 10.1111/cea.12250.
Trees belonging to the order of Fagales show a distinct geographical distribution. While alder and birch are endemic in the temperate zones of the Northern Hemisphere, hazel, hornbeam and oak prefer a warmer climate. However, specific immunotherapy of Fagales pollen-allergic patients is mainly performed using birch pollen extracts, thus limiting the success of this intervention in birch-free areas.
T cells are considered key players in the modification of an allergic immune response during specific immunotherapy (SIT), therefore we thought to combine linear T cell epitope-containing stretches of the five most important Fagales allergens from birch, hazel, alder, oak and hornbeam resulting in a Fagales pollen hybrid (FPH) molecule applicable for SIT.
A Fagales pollen hybrid was generated by PCR-based recombination of low IgE-binding allergen epitopes. Moreover, a structural-variant FPH4 was calculated by in silico mutagenesis, rendering the protein unable to adopt the Bet v 1-like fold. Both molecules were produced in Escherichia coli, characterized physico-chemically as well as immunologically, and tested in mouse models of allergic sensitization as well as allergy prophylaxis.
Using spectroscopic analyses, both proteins were monomeric, and the secondary structure elements of FPH resemble the ones typical for Bet v 1-like proteins, whereas FPH4 showed increased amounts of unordered structure. Both molecules displayed reduced binding capacities of Bet v 1-specific IgE antibodies. However, in a mouse model, the proteins were able to induce high IgG titres cross-reactive with all parental allergens. Moreover, prophylactic treatment with the hybrid proteins prevented pollen extract-induced allergic lung inflammation in vivo.
The hybrid molecules showed a more efficient uptake and processing by dendritic cells resulting in a modified T cell response. The proteins had a lower IgE-binding capacity compared with the parental allergens, thus the high safety profile and increased efficacy emphasize clinical application for the treatment of Fagales multi-sensitization.
属于壳斗目(山毛榉目)的树木表现出明显的地理分布。虽然桤木和桦木是北半球温带特有的,榛子、榉木和栎木则更喜欢温暖的气候。然而,对壳斗目花粉过敏患者的特异性免疫治疗主要使用桦树花粉提取物进行,因此这限制了该干预措施在无桦树地区的效果。
T 细胞被认为是特异性免疫治疗(SIT)中改变过敏免疫反应的关键因素,因此我们考虑将桦树、榛子、桤木、栎木和榉木这五种最重要的壳斗目过敏原中含有线性 T 细胞表位的片段进行组合,从而产生一种适用于 SIT 的壳斗目花粉杂合(FPH)分子。
通过基于 PCR 的重组,将低 IgE 结合过敏原表位的壳斗目花粉杂合分子产生。此外,通过计算机诱变计算出一种结构变异的 FPH4,使该蛋白无法采用 Bet v 1 样折叠。这两种分子均在大肠杆菌中产生,通过物理化学和免疫学特性进行了表征,并在过敏致敏和过敏预防的小鼠模型中进行了测试。
使用光谱分析,两种蛋白均为单体,且 FPH 的二级结构元件与 Bet v 1 样蛋白的典型元件相似,而 FPH4 则显示出更多的无序结构。两种分子均显示出降低的与 Bet v 1 特异性 IgE 抗体的结合能力。然而,在小鼠模型中,这些蛋白能够诱导与所有亲本过敏原发生交叉反应的高 IgG 滴度。此外,预防性使用杂合蛋白治疗可防止花粉提取物在体内诱导过敏的肺部炎症。
杂合分子通过树突状细胞的摄取和处理显示出更高的效率,从而导致 T 细胞反应发生改变。与亲本过敏原相比,这些蛋白的 IgE 结合能力较低,因此高安全性和更高的疗效强调了其在治疗壳斗目多敏化方面的临床应用。