Procedure for a standardized preparation of skin prick test solutions for the diagnosis of occupational type I allergies in the absence of commercial extracts.

Allergologie select Pub Date : 2024-07-04 eCollection Date: 2024-01-01 DOI:10.5414/ALX02506E
Sabine Kespohl, Robin Jost, Silke Maryska, Lena-Maria Altin, Ingrid Sander, Stefan Schülke, Kathrin E Paulus-Tremel, Andreas Bonertz, Thomas Klose, Vera Mahler, Monika Raulf
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Abstract

In order to ensure valid diagnostics for occupational test allergen solutions despite the ongoing reduction in the availability of commercial test extracts, a plan B was initiated for the possible production of skin prick test (SPT) solutions in public pharmacies. For important occupational allergen sources (wheat and rye, storage mites, animal epithelia, mold material) laboratory extraction methods were analyzed in comparison to pharmacy compatible extraction methods regarding protein quantity and quality in SDS-PAGE combined with silver staining. Subsequently, using the example of bovine epithelia, adapted extraction procedures as well as in-process and final product controls were transferred to a public pharmacy. Allergen sources with a high protein content, such as wheat and rye grains as well as storage mites, showed good comparability of the extractable protein quantity and protein pattern, regardless of the applied extraction method. In contrast, allergen source materials with a low total protein content, such as animal epithelia and molds, can benefit from laboratory extraction conditions such as mechanical disruption and specific buffer additives. In the qualitative protein silver staining, characteristic protein patterns were identified for each allergen source. Depending on the extraction method, only minor differences in total protein patterns were observed in animal epithelia and molds. Using source materials from two suppliers, the resulting allergen extracts displayed clear differences in protein content in storage mites and quantitative and qualitative differences in molds. A practical preparation attempt of SPT solutions in a public pharmacy was successful. SPT solutions prepared with adapted pharmacy extraction methods showed a comparable protein and Bos d 2 allergen content and equivalent qualities in the protein pattern compared to a previously available commercial SPT solution. Accordingly, it can be assumed that standardized SPT solutions with sufficient allergen quality for occupational allergen sources can be prepared in public pharmacies if certified allergen sources with appropriate protein content are available.

在没有商业提取物的情况下,用于诊断 I 型职业性过敏的皮肤点刺试验溶液的标准化制备程序。
尽管商业测试提取物的供应量不断减少,但为了确保职业测试过敏原溶液的有效诊断,我们启动了一项 B 计划,以便在公共药房生产皮肤点刺测试 (SPT) 溶液。针对重要的职业过敏原来源(小麦和黑麦、贮藏螨、动物上皮、霉菌材料),将实验室提取方法与药房兼容提取方法进行了比较分析,以确定 SDS-PAGE 结合银染色法提取的蛋白质数量和质量。随后,以牛上皮细胞为例,将经过调整的提取程序以及过程控制和最终产品控制转移到公共药房。蛋白质含量较高的过敏源,如小麦和黑麦谷物以及贮藏螨,无论采用哪种提取方法,其可提取的蛋白质数量和蛋白质模式都具有良好的可比性。相比之下,总蛋白含量较低的过敏源材料,如动物上皮和霉菌,可从实验室提取条件中获益,如机械破坏和特定的缓冲添加剂。在蛋白质银染色定性分析中,每种过敏源都能识别出特有的蛋白质模式。根据提取方法的不同,在动物上皮和霉菌中观察到的总蛋白模式只有细微差别。使用来自两家供应商的源材料,所提取的过敏原在贮存螨的蛋白质含量上有明显差异,在霉菌的数量和质量上也有差异。在一家公共药房实际制备 SPT 溶液的尝试取得了成功。与之前市面上销售的 SPT 溶液相比,采用药房萃取方法制备的 SPT 溶液中蛋白质和 Bos d 2 过敏原含量相当,蛋白质模式的质量也相当。因此,可以认为,如果有经认证的、蛋白质含量适当的过敏原来源,公共药房可以制备出具有足够过敏原质量的标准化 SPT 溶液,用于职业过敏原来源。
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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