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首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Clinical characteristics of soybean allergy in Europe: a double-blind, placebo-controlled food challenge study.
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Clinical characteristics of soybean allergy in Europe: a double-blind, placebo-controlled food challenge study.

机译:欧洲大豆过敏的临床特征:一项双盲,安慰剂对照食物挑战研究。

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BACKGROUND: Soybean is a relevant allergenic food, but little is known about individual threshold doses in soy allergy. OBJECTIVE: We sought to determine the clinical characteristics of soy allergy in Europe, including a dose-response curve. METHODS: Patients with a history of soy allergy underwent a titrated, double-blind, placebo-controlled food challenge. A statistical model was used to calculate the risk of allergic consumers to experience an allergic reaction to soy. Sera were analyzed for specific IgE to soy, peanut, Bet v 1, and Gly m 4. RESULTS: All patients but one responded primarily with subjective symptoms to the challenge followed by objective symptoms in 11 subjects, ranging from rhinitis up to a decrease in blood pressure. Cumulative threshold doses for allergic reactions ranged from 10 mg to 50 g for subjective symptoms and from 454 mg to 50 g for objective symptoms. The pattern of IgE reactivity against proteins with molecular weights of between approximately 10 and 70 kd was highly individual among the patients and did not correlate with the severity of symptoms. CONCLUSIONS: When data are fitted by using a normal distribution statistical model, they predict that 1% of patients with soy allergy would react subjectively and objectively with 0.21 and 37.2 mg of soy protein, respectively. CLINICAL IMPLICATIONS: Both the clinical and immunologic basis of soy allergy in Europe are highly complex, which affects the diagnosis of soy allergy and the advice given to patients with soy allergy in regard to risk management.
机译:背景:大豆是一种相关的致敏食品,但对大豆过敏的个体阈值剂量知之甚少。目的:我们试图确定欧洲大豆过敏的临床特征,包括剂量反应曲线。方法:具有大豆过敏史的患者接受了滴定,双盲,安慰剂控制的食物刺激。使用统计模型来计算过敏的消费者经历对大豆过敏反应的风险。结果分析了血清中大豆,花生,Bet v 1和Gly m 4的特异性IgE。结果:11名受试者中,除一名受试者外,其他所有受试者均主要对攻击产生主观症状,随后出现客观症状,从鼻炎到降低。血压。对于主观症状,过敏反应的累积阈值剂量为10 mg至50 g,对于客观症状,其累积阈值剂量为454 mg至50 g。 IgE对分子量在10到70 kd之间的蛋白质的反应性模式在患者中高度个体化,并且与症状的严重程度无关。结论:使用正态分布统计模型拟合数据时,他们预测1%的大豆过敏患者将分别对0.21和37.2 mg大豆蛋白进行主观和客观反应。临床意义:在欧洲,大豆过敏的临床和免疫学基础都非常复杂,这会影响大豆过敏的诊断以及对大豆过敏患者的风险管理建议。

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