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首页> 外文期刊>Clinical and experimental allergy : >Comparison of allergenicity and immunogenicity of an intact allergen vaccine and commercially available allergoid products for birch pollen immunotherapy.
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Comparison of allergenicity and immunogenicity of an intact allergen vaccine and commercially available allergoid products for birch pollen immunotherapy.

机译:完整的过敏原疫苗和用于桦树花粉免疫疗法的市售过敏原产品的过敏原和免疫原性的比较。

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BACKGROUND: Specific immunotherapy with intact allergen vaccine is a well-documented treatment for allergic diseases. Different vaccine formulations are currently commercially available, the active ingredient either being intact allergens or chemically modified allergoids. The rationale behind allergoids is to decrease allergenicity while maintaining immunogenicity. However, data from the German health authorities based on reporting of adverse events over a 10-year period did not indicate increased safety of allergoids over intact allergens. OBJECTIVE: The objective of this study was to investigate the effect of chemical modification on allergenicity and immunogenicity comparing four commercial allergoid products for birch pollen immunotherapy with an intact allergen vaccine. METHODS: Solid-phase IgE inhibition and histamine release assays were selected as model systems for allergenicity, and a combination of human T cell proliferation and IgG titres following mouse immunizations were used to address the immunogenicity of the intact allergen vaccine and the four allergoids. In all assays, the products were normalized with respect to the manufacturer's recommended maintenance dose. RESULTS: IgE inhibition experiments showed a change in epitope composition comparing intact allergen vaccine with allergoid. One allergoid product induced enhanced histamine release compared to the intact allergens, while the other three allergoids showed reduced release. Standard T cell stimulation assays using lines from allergic patients showed a reduced response for all allergoids compared with the intact allergen vaccine regardless of the cell type used for antigen presentation. All allergoids showed reduced capacity to induce allergen-specific IgG responses in mice. CONCLUSION: While some allergoids were associated with reduced allergenicity, a clear reduction in immunogenicity was observed for all allergoid products compared with the intact allergen vaccine, and the commercial allergoids tested therefore do not fulfil theallergoid concept.
机译:背景:完整的过敏原疫苗的特异性免疫疗法是治疗过敏性疾病的有据可查的疗法。当前可商购获得不同的疫苗制剂,其活性成分是完整的过敏原或化学修饰的过敏原。过敏原的基本原理是减少过敏原,同时保持免疫原性。但是,德国卫生当局基于10年期间不良事件报告的数据并未表明变态反应变体相对于完整变应原的安全性增加。目的:本研究的目的是比较四种完整的变应原疫苗用于桦树花粉免疫疗法的四种商品变应性变应原产品,以研究化学修饰对变应原性和免疫原性的影响。方法:选择固相IgE抑制和组胺释放试验作为变应原性的模型系统,并使用小鼠免疫后人T细胞增殖和IgG滴度的组合来解决完整变应原疫苗和四种变应原的免疫原性。在所有测定中,均根据制造商建议的维持剂量对产品进行了标准化。结果:IgE抑制实验表明,与完整的变应原疫苗和变应原疫苗相比,表位组成发生了变化。与完整的变应原相比,一种变应原产品可诱导增强的组胺释放,而其他三种变应原则显示减少的释放。与完整的过敏原疫苗相比,使用来自过敏患者的品系进行的标准T细胞刺激试验显示,对于所有过敏原,其应答均降低,而与用于抗原呈递的细胞类型无关。所有变态反应动物均表现出降低诱导小鼠变应原特异性IgG反应的能力。结论:虽然有些变应原性与变应原性降低有关,但与完整的变应原疫苗相比,所有变应原性产品均观察到免疫原性明显降低,因此测试的商业化变应性变体不符合变应原性概念。

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