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Biological standardization and maximum tolerated dose estimation of an Alternaria alternata allergenic extract

机译:链格孢变应原提取物的生物学标准化和最大耐受剂量估计

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Background: The manufacture of allergenic extracts from the mold Alternaria alternata is influenced by factors such as strain variability, allergenic origin, culturing conditions and extraction process, which affect the reproducibility of the preparations intended for diagnostic and therapeutic use.Objectives: To select the most adequate antigenic source of A. alternata extracts and determine its maximum tolerated dose (MTD) to be used in a subsequent immunotherapy efficacy clinical trial.Methods: Twenty-one patients monosensitized to A. alternata were involved in a biological standardization process of A. alternata extracts. Four different mold strains were cultured and used to produce extracts by three different methods, each incorporating proteins from different origins: culture filtrate, buffer extractable fraction and cellular antigens. The selected extract, characterized as in-house reference (IHR) preparation was used in a MTD finding immunotherapy study. Serum IgE, IgG, IgG1 and IgG4 specific of complete extract and purified natural and recombinant forms of Alt a 1 were determined by different EIA methods.Results: Culture filtrate extract containing the allergens secreted to the spent medium was shown to be the most adequate option for establishing an IHR preparation for A. alternata extract manufacturing. A maximum dose of 1670 UBE, equivalent to 0.1 μg Alt a 1, was determined as MTD for immunotherapy. One year of administration of such a dose at monthly intervals elicited pronounced immunological changes with statistically significant decreases in IgE and increases in IgG4, both estimated with whole extract or purified Alt a 1.Conclusion: A high quality natural A. alternata extract has been developed and preliminarily tested to define its MTD for subsequent determination of the optimal dose in an immunotherapy efficacy clinical trial. Keywords: Mold allergy, mold immunotherapy, specific antibodies, in-house reference, Alt a 1, recombinant allergens.
机译:背景:交替链霉菌(Alternaria alternata)霉菌的变应原提取物的生产受菌株变异性,变应原起源,培养条件和提取过程等因素的影响,这些因素会影响用于诊断和治疗用途的制剂的可重复性。方法:二十一株对交链孢霉单敏的患者参与了交链孢霉的生物学标准化过程,并确定其最大耐受剂量(MTD),以用于后续的免疫疗法临床试验。提取物。培养了四种不同的霉菌菌株,并通过三种不同的方法用于生产提取物,每种方法都结合了来自不同来源的蛋白质:培养滤液,可提取缓冲液的部分和细胞抗原。选定的以内部参考(IHR)制剂为特征的提取物用于MTD查找免疫疗法研究。通过不同的EIA方法测定完全提取物的特异血清IgE,IgG,IgG1和IgG4以及纯化的Alt a 1的天然和重组形式的结果。结果:培养滤液提取物中含有分泌到用过的培养基中的过敏原是最合适的选择建立一种适用于交链曲霉提取物生产的《国际卫生条例》制剂。确定最大剂量1670 UBE(相当于0.1μgAlt a 1)作为免疫治疗的MTD。以全间隔提取物或纯化的Alt a估计,以每月间隔给药一年的剂量可引起明显的免疫学改变,IgE显着降低,IgG4显着增加。结论:已开发出一种高质量的天然链球菌提取物。并经过初步测试以定义其MTD,以便随后在免疫疗法功效临床试验中确定最佳剂量。关键字:霉菌过敏,霉菌免疫治疗,特异性抗体,内部参考,Alt a 1,重组过敏原。

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