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Quantification of Chemical Peptide Reactivity for Screening Contact Allergens: A Classification Tree Model Approach

机译:筛选接触性过敏原的化学肽反应性的量化:分类树模型方法

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In the interest of reducing animal use, in vitro alternatives for skin sensitization testing are under development. One unifying characteristic of chemical allergens is the requirement that they react with proteins for the effective induction of skin sensitization. The majority of chemical allergens are electrophilic and react with nucleophilic amino acids. To determine whether and to what extent reactivity correlates with skin sensitization potential, 82 chemicals comprising allergens of different potencies and nonallergenic chemicals were evaluated for their ability to react with reduced glutathione (GSH) or with two synthetic peptides containing either a single cysteine or lysine. Following a 15-min reaction time with GSH, or a 24-h reaction time with the two synthetic peptides, the samples were analyzed by high-performance liquid chromatography. UV detection was used to monitor the depletion of GSH or the peptides. The peptide reactivity data were compared with existing local lymph node assay data using recursive partitioning methodology to build a classification tree that allowed a ranking of reactivity as minimal, low, moderate, and high. Generally, nonallergens and weak allergens demonstrated minimal to low peptide reactivity, whereas moderate to extremely potent allergens displayed moderate to high peptide reactivity. Classifying minimal reactivity as nonsensitizers and low, moderate, and high reactivity as sensitizers, it was determined that a model based on cysteine and lysine gave a prediction accuracy of 89%. The results of these investigations reveal that measurement of peptide reactivity has considerable potential utility as a screening approach for skin sensitization testing, and thereby for reducing reliance on animal-based test methods.
机译:为了减少动物的使用,用于皮肤敏化测试的体外替代品正在开发中。化学变应原的一个统一特征是要求它们与蛋白质反应以有效诱导皮肤致敏。大多数化学过敏原是亲电子的,并与亲核氨基酸反应。为了确定反应性是否与皮肤敏化潜能相关以及在多大程度上与皮肤致敏潜能相关,评估了82种包含不同效力过敏原和非过敏原化学物质与还原型谷胱甘肽(GSH)或与两种含有单个半胱氨酸或赖氨酸的合成肽反应的能力。与GSH反应15分钟或与两种合成肽反应24小时后,通过高效液相色谱分析样品。紫外线检测用于监测GSH或肽的消耗。使用递归分配方法将肽反应性数据与现有的局部淋巴结测定数据进行比较,以建立分类树,该树可将反应性分级为最小,低,中和高。通常,非过敏原和弱过敏原表现出极低至低的肽反应性,而中度至极强的过敏原则表现出中至高肽反应性。将最小反应性归类为非敏化剂,将低,中和高反应性归类为敏化剂,可以确定基于半胱氨​​酸和赖氨酸的模型的预测准确性为89%。这些研究的结果表明,肽反应性的测量作为皮肤敏化测试的筛选方法具有相当大的潜在实用性,从而减少了对基于动物的测试方法的依赖。

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