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MALDI-TOF MS analysis of labile Lolium perenne major allergens in mixes.

机译:混合物中不稳定的黑麦草主要变应原的MALDI-TOF MS分析。

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BACKGROUND: It is well known that allergen extracts used for specific therapy of allergic disorders are commonly stored as mixtures, causing an alteration of its stability. OBJECTIVE: The aim of this report is to identify pollen allergens susceptible to degradation during storage of mixtures containing different sources of proteases in the absence of glycerol as a preserving agent. METHODS: Mixes containing Lolium perenne (Lol p) pollen extract with either Aspergillus fumigatus or Periplaneta americana extracts were prepared and co-incubated for 90 days at 4 degrees C. Samples were taken off at fixed times and comparatively tested by in vitro and in vivo assays with atopic patients. Selected pollinic allergens were subjected to MALDI-TOF MS analysis. RESULTS: ELISA inhibition evidenced the loss of potency from ryegrass extract, and immunoblotting assays showed the degradation of specific pollinic allergens during storage of mixtures containing protease-rich sources. An in vivo intradermal skin assay confirmed the gradual loss of the biological activity of L. perenne pollen extract co-incubated with non-related protease-rich extracts in comparison with that of the control pollen extract. MALDI-TOF MS analysis allowed us to determine that Lol p 1 and Lol p 5 are susceptible to proteolysis whereas Lol p 4 was found to be resistant to degradation during storage. CONCLUSIONS: Lol p 1 and Lol p 5 degradation is responsible for the loss of the biological activity of L. perenne pollen extract when co-incubated with protease-rich fungal and cockroach extracts in the same vial for months in the absence of glycerol as a preserving agent. The integrity of these major allergens must be preserved to increase the vaccine stability and to assure efficacy when mixes are used for immunotherapy.
机译:背景:众所周知,用于特异性治疗过敏性疾病的过敏原提取物通常以混合物形式存储,从而改变其稳定性。目的:本报告旨在鉴定在不存在甘油作为防腐剂的情况下,在储存含有不同蛋白酶来源的混合物的过程中易于降解的花粉过敏原。方法:制备含有黑麦草(Lol p)花粉提取物与烟曲霉或美洲大黄Per提取物的混合物,并在4°C下共孵育90天。在固定时间取出样品,并通过体内和体外进行比较测试特应性患者的检测。对选定的花粉过敏原进行MALDI-TOF MS分析。结果:ELISA抑制作用证明了黑麦草提取物的效力丧失,免疫印迹分析表明,在储存富含蛋白酶的混合物的过程中,特定的花粉过敏原降解了。与对照花粉提取物相比,体内皮内皮肤试验证实了与不相关的富含蛋白酶的提取物共孵育的紫苏花粉花粉提取物的生物活性逐渐丧失。 MALDI-TOF MS分析使我们能够确定Lol p 1和Lol p 5易于蛋白水解,而Lol p 4被发现在储存过程中具有抗降解性。结论:Lol p 1和Lol p 5的降解是与富含蛋白酶的真菌和蟑螂提取物在同一小瓶中共孵育几个月而不存在甘油的情况下,紫苏花粉提取物的生物学活性降低的原因。防腐剂。当将这些混合物用于免疫治疗时,必须保留这些主要过敏原的完整性,以提高疫苗的稳定性并确保功效。

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