首页> 外文期刊>International archives of allergy and immunology >The Russian Thistle (Salsola kali) pollen major allergen, Sal k 1, can be quantified in allergenic extracts and airborne pollen.
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The Russian Thistle (Salsola kali) pollen major allergen, Sal k 1, can be quantified in allergenic extracts and airborne pollen.

机译:俄罗斯蓟(Salsola kali)花粉主要过敏原,Sal k 1,可以在过敏原提取物和空中花粉中定量。

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BACKGROUND: Russian thistle (Salsola kali) pollen is an important cause of pollinosis in areas where rainfall is not abundant. Our aim was to develop an ELISA for quantification of the major allergen of S. kali extracts, Sal k 1, and to assess the correlation of this allergen content with the allergenic activity of extracts. METHODS: Sal k 1 was purified by ion exchange and gel permeation chromatography and identified by mass spectrometry. Monoclonal antibody 4C11 was used for capture at 5 microg/ml and biotin-labeled specific antiserum at 0.25 microg/ml served for detection. The allergenic activity of the pollen extracts was measured by enzyme allergosorbent test inhibition. RESULTS: Sal k 1 reacted to 85% of sera from 40 S. kali-allergic patients and was able to inhibit 92% of the IgE-binding capacity of patients' serum pool to the whole extract. The ELISA had a lineal range between 1.25 and 20 ng/ml of purified Sal k 1. The intra- and interassay coefficients of variation were lower than 5 and 10%, respectively. The assay was very sensitive since it had a detection limit of 0.08 ng/ml. No reactivity was found outside the Amaranthaceae family where only Kochia and Salicornia sp. gave significant reactivity. A good correlation (Spearman's rho = 0.92) was obtained between Sal k 1 content of different S. kali extracts and their IgE-binding activity. CONCLUSIONS: The results proved the usefulness of the two-site sandwich ELISA for aeroallergen control and for the standardization of S. kali pollen extracts intended for clinical use.
机译:背景:俄罗斯蓟(Salsola kali)花粉是降雨量不足的地区授粉的重要原因。我们的目的是开发一种ELISA方法,用于定量分析卡利链球菌提取物的主要变应原,Sal k 1,并评估该变应原含量与提取物的变应原活性之间的相关性。方法:Salk 1通过离子交换和凝胶渗透色谱法纯化,并通过质谱鉴定。单克隆抗体4C11用于捕获,浓度为5微克/毫升,生物素标记的特异性抗血清为0.25微克/毫升,用于检测。花粉提取物的变应原活性通过酶变应原吸附试验抑制来测量。结果:Sal k 1对来自40名卡里氏酵母过敏患者的85%的血清有反应,并且能够抑制患者血清库对整个提取物的IgE结合能力的92%。 ELISA的线性范围介于1.25和20 ng / ml的纯化Salk 1之间。测定内和测定间变异系数分别低于5%和10%。该测定法的检测极限为0.08 ng / ml,因此非常敏感。在A菜科以外的地方仅发现了Kochia和Salicornia sp.。具有明显的反应性。不同S. kali提取物的Sal k 1含量与其IgE结合活性之间具有良好的相关性(Spearman的rho = 0.92)。结论:结果证明了两点夹心ELISA在控制气变应原和标准化供临床使用的加里链球菌花粉提取物中的有用性。

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