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重组屋尘螨变应原

Recombinant house dust mite allergens.

作者信息

Vrtala Susanne, Huber Hans, Thomas Wayne R

机构信息

Division of Immunopathology, Department of Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.

Biomay AG, Lazarettgasse 19. 1090 Vienna, Austria.

出版信息

Methods. 2014 Mar 1;66(1):67-74. doi: 10.1016/j.ymeth.2013.07.034. Epub 2013 Jul 31.

Abstract

House dust mites (HDM) are a globally important source of allergen responsible for the sensitization of more than 50% of allergic patients. Specific immunotherapy with HDM extracts is effective but allergen extracts cannot be fully standardized and severe side-effects can occur during the protracted course of treatment. The introduction of molecular biological techniques into allergy research allowed the indentification of more than 20 groups of HDM allergens. Recombinant HDM allergens can be produced in defined concentrations and consistent quality and allow the development of vaccines for HDM allergy with reduced allergenic activity and retained immunogenicity. The immunotherapy trials in pollen allergic patients with recombinant pollen allergens/hypoallergenic allergen derivatives have shown that this treatment is effective and indicated that recombinant HDM vaccines might improve immunotherapy of HDM allergic patients. Here we report the steps for the development of vaccines for HDM allergy. After selection of the most prevalent HDM species, the panel of allergens to be included into a therapeutic vaccine for HDM allergy needs to be determined. HDM allergens with high IgE-binding frequency and clinical relevance will be modified into hypoallergenic variants and evaluated for their allergenic activity and immunogenicity. Derivatives with reduced allergenic activity but with retained immunogenicity would be good candidates for a HDM vaccine for safe and efficient immunotherapy.

摘要

屋尘螨(HDM)是全球重要的过敏原来源,导致超过50%的过敏患者致敏。用HDM提取物进行特异性免疫疗法是有效的,但过敏原提取物无法完全标准化,且在长期治疗过程中可能会出现严重的副作用。分子生物学技术引入过敏研究后,已鉴定出20多组HDM过敏原。重组HDM过敏原可以以确定的浓度和一致的质量生产,并有助于开发具有降低的过敏原活性和保留免疫原性的HDM过敏疫苗。对花粉过敏患者使用重组花粉过敏原/低变应原性过敏原衍生物进行的免疫疗法试验表明,这种治疗方法是有效的,并表明重组HDM疫苗可能会改善HDM过敏患者的免疫疗法。在此,我们报告HDM过敏疫苗的研发步骤。在选择最常见的HDM种类后,需要确定纳入HDM过敏治疗疫苗的过敏原组合。具有高IgE结合频率和临床相关性的HDM过敏原将被改造为低变应原性变体,并评估其过敏原活性和免疫原性。过敏原活性降低但免疫原性保留的衍生物将是用于安全有效免疫疗法的HDM疫苗的良好候选物。

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