Validation of an ELISA method for quantification of the major Timothy grass pollen allergen Phl p 5a (BSP090).

Q4 Medicine
Pharmeuropa bio & scientific notes Pub Date : 2022-01-01
J Zimmer, S Schmidt, A Costanzo, K-H Buchheit, S Brown, J Carnés, M Chapman, A Chen, M De Neergaard, S Döring, J Hindley, T Holzhauser, S Jorajuria, D Le Tallec, M Lombardero, P Iacovacci, G Reese, I Sander, B Smith, D Strecker, R van Ree, M Zebina, S Kaul, S Vieths
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引用次数: 0

Abstract

Progress towards standardisation of allergen products has been made in recent years. Nevertheless, no standardised test method to quantify the allergen content of grass pollen allergen products is available at present. One aim of the BSP090 project was to validate a quantitative assay for a major Timothy grass (Phleum pratense) pollen allergen, Phl p 5. Qualification of a candidate ELISA system was performed with regard to range, robustness and cross-reactivity in preliminary studies. The assay specifically detected Phl p 5 with a quantification range from 3.9 ng/mL to 62.5 ng/mL. Suitability to quantify recombinant and natural Phl p 5 was further assessed in a collaborative study including 14 laboratories in Europe and the USA. Precision and accuracy of the assay was satisfactory with 93% of calculated Phl p 5 concentrations and 100% of total recoveries being within the ± 30% acceptance range. Similar results were obtained for spike recoveries, with exclusion of the lowest concentration spike, showing spike recoveries exceeding the acceptance range for six laboratories. Inter-assay (repeatability) and inter-laboratory (reproducibility) variability were satisfactory, in the format used in the present study. Robustness towards different statistical methods for data analysis was demonstrated. In conclusion, the assay can easily be established in routine testing and results of the preliminary testing and collaborative study support the proposal of the assessed Phl p 5-specific ELISA as a European Pharmacopoeia general method.

建立了一种定量测定蒂莫西草花粉主要过敏原php5a (BSP090)的ELISA方法。
近年来,在过敏原产品标准化方面取得了进展。然而,目前还没有标准化的测试方法来量化草花粉过敏原产品的过敏原含量。BSP090项目的目的之一是验证一种主要的蒂莫西草(Phleum pratense)花粉过敏原php5的定量分析方法。在初步研究中对候选ELISA系统的范围、稳健性和交叉反应性进行了鉴定。特异性检测php5,定量范围为3.9 ~ 62.5 ng/mL。在一项包括欧洲和美国的14个实验室的合作研究中,进一步评估了重组和天然php5的量化适用性。该方法精密度和准确度令人满意,计算的php5浓度93%,总回收率100%在±30%的可接受范围内。在排除最低浓度峰后,得到了类似的结果,表明峰回收率超过了六个实验室的可接受范围。在本研究中使用的格式中,测定间(可重复性)和实验室间(可重复性)变异性令人满意。对数据分析的不同统计方法的稳健性进行了论证。总之,该方法可以很容易地建立在常规检测中,初步测试和合作研究的结果支持评估的php5特异性ELISA作为欧洲药典通用方法的建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmeuropa bio & scientific notes
Pharmeuropa bio & scientific notes Medicine-Medicine (all)
CiteScore
0.70
自引率
0.00%
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