过敏疫苗:需要对主要过敏原的大量单位进行标准化。

Pharmeuropa bio Pub Date : 2005-09-01
R van Ree, J W Dorpema, S Vieths
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引用次数: 0

摘要

呼吸道过敏的治疗可以使用过敏原提取物进行过敏原特异性免疫治疗。这些产品是具有极其复杂和可变组成的生物制剂。只有少数成分对这种疾病具有重要意义,即所谓的主要过敏原。目前,过敏原提取物的标准化主要是通过收集过敏患者的血清来确定它们的整体ige结合能力。市场上的每家公司都使用自己的单位类型来表达实力,从而阻碍了可比性。另一个缺点是主要过敏原组成不确定。大多数公司在其质量控制系统中引入了测量主要过敏原的分析方法,但这些数据尚未用于标签目的。在标准化方案中纳入主要过敏原含量的必要性现已被广泛接受。为了支持未来以主要过敏原含量为基础的标签,欧盟资助了多学科多中心项目CREATE。本项目旨在为最重要的主要呼吸道过敏原制定经国际认证的参考资料,并评估可用的酶联免疫吸附法测量过敏原的性能。该项目将促进通过活性成分(主要过敏原)含量来表达效力,并将允许直接比较竞争产品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Allergy vaccines: a need for standardisation in mass units of major allergen.

Treatment of respiratory allergies can be performed with allergen-specific immunotherapy using allergen extracts. These products are biologicals with an extremely complex and variable composition. Only a few components are of major importance for the disease, the so-called major allergens. At present, standardisation of allergen extracts is dominated by techniques that aim at establishing their overall IgE-binding potencies using pooled sera of allergic patients. Each company in the market uses its own type of units to express potencies, thus hampering comparability. Another disadvantage is that the major allergen composition is not determined. Most companies have introduced assays for the measurement of major allergens in their quality control systems, but these data are not yet used for labelling purposes. The need to include major allergen content in standardisation protocols is now widely accepted. To support future labelling on the basis of major allergen content the European Union has funded the multidisciplinary multicentre project CREATE. This project aims at developing international certified references for the most important major respiratory allergens and at evaluating the performance of available ELISA for their measurement. The project will facilitate expression of potencies by active ingredient (major allergen) content and will allow direct comparison of competitor products.

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